cells Article The E1a Adenoviral Gene Upregulates the Yamanaka Factors to Induce Partial Cellular Reprogramming Gracia Mendoza 1,2, * , Rebeca González-Pastor 1,3, * , Juan Miguel Sánchez 4 , Altamira Arce-Cerezo 5 , Miguel Quintanilla 6 , Gema Moreno-Bueno 6,7,8 , Anna Pujol 5 , Carolina Belmar-López 1,9 , Alba de Martino 1 , Efrén Riu 5 , Tristan A. Rodriguez 4 and Pilar Martin-Duque 1,2,8,10,11, * 1 Instituto Aragonés de Ciencias de la Salud (IACS), 50009 Zaragoza, Spain 2 Instituto de Investigación Sanitaria Aragón (IIS Aragón), 50009 Zaragoza, Spain 3 Centro de Investigación Biomédica (CENBIO), Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito 170527, Ecuador 4 National Heart and Lung Institute, Imperial College London, London W12 ONN, UK 5 Centro de Biotecnología Animal y de Terapia Génica (CBATEG), Universidad Autónoma de Barcelona, 08193 Bellaterra, Spain 6 Departamento de Bioquímica, Instituto de Investigaciones Biomédicas ‘Alberto Sols’, Universidad Autónoma de Madrid (UAM), (UAM-CSIC), 28029 Madrid, Spain 7 Fundación MD Anderson Internacional, 28033 Madrid, Spain 8 Centro de Investigación Biomédica en Red, Instituto de Salud Carlos III, Red de Cáncer (CIBERONC) and Red de Nanomedicina y Nanomateriales (CIBER-BBN), 28029 Madrid, Spain 9 OncoGenomics Lab, Universidad Privada San Juan Bautista, Lima 15038, Peru 10 Fundación Araid, 50018 Zaragoza, Spain 11 Departamento de Cirugía, Facultad de Medicina, Universidad de Zaragoza, 50009 Zaragoza, Spain * Correspondence: gmendoza@iisaragon.es (G.M.); rebeca.gonzalez@ute.edu.ec (R.G.-P.); mariadelpilar.martin@unizar.es (P.M.-D.); Tel.: +34-976-71-5895 (P.M.-D.) Abstract: The induction of pluripotency by enforced expression of different sets of genes in somatic Citation: Mendoza, G.; cells has been achieved with reprogramming technologies first described by Yamanaka’s group. González-Pastor, R.; Sánchez, J.M.; Methodologies for generating induced pluripotent stem cells are as varied as the combinations of Arce-Cerezo, A.; Quintanilla, M.; genes used. It has previously been reported that the adenoviral E1a gene can induce the expression Moreno-Bueno, G.; Pujol, A.; of two of the Yamanaka factors (c-Myc and Oct-4) and epigenetic changes. Here, we demonstrate that Belmar-López, C.; de Martino, A.; the E1a-12S over-expression is sufficient to induce pluripotent-like characteristics closely to epiblast Riu, E.; et al. The E1a Adenoviral stem cells in mouse embryonic fibroblasts through the activation of the pluripotency gene regulatory Gene Upregulates the Yamanaka network. These findings provide not only empirical evidence that the expression of one single factor Factors to Induce Partial Cellular is sufficient for partial reprogramming but also a potential mechanistic explanation for how viral Reprogramming. Cells 2023, 12, 1338. infection could lead to neoplasia if they are surrounded by the appropriate environment or the right https://doi.org/10.3390/ medium, as happens with the tumorogenic niche. cells12091338 Academic Editor: Ritva Tikkanen Keywords: reprogramming; induced pluripotent stem cells; embryonic stem cells; Yamanaka factors; adenovirus; E1a gene Received: 29 January 2023 Revised: 29 April 2023 Accepted: 2 May 2023 Published: 7 May 2023 1. Introduction Cellular reprogramming of somatic cells has been one of the fundamental questions in stem cell biology. A major breakthrough in this field was achieved when it was demon- Copyright: © 2023 by the authors. strated that embryonic and adult somatic cells could be reprogrammed to the pluripotent Licensee MDPI, Basel, Switzerland. state just by overexpression of four defined genes, c-Myc, Klf4, Oct4, and Sox2 [1,2]. The This article is an open access article combination of these four factors has been subsequently termed the Yamanaka factors, and distributed under the terms and the resulting reprogrammed cells are defined as induced pluripotent stem (iPS) cells. This conditions of the Creative Commons ability to reprogram somatic cells has created enormous expectations, given the potential Attribution (CC BY) license (https:// clinical applications of these iPS cells. For example, to facilitate the generation of patient- creativecommons.org/licenses/by/ specific stem cells that would overcome the ethical problems posed by human embryonic 4.0/). Cells 2023, 12, 1338. https://doi.org/10.3390/cells12091338 https://www.mdpi.com/journal/cells Cells 2023, 12, 1338 2 of 17 stem cells (ESCs) and reduce the risk of immune rejection [3]. For these reasons, stem cell researchers have invested significant efforts in improving both the efficiency and the technical limitations that accompany the reprogramming process. As part of this effort, a number of studies have reported various mechanisms for enhancing the efficiency and rate of reprogramming, for example, by using small molecules [4–6]. Another major effort has been to identify cell types where it is possible to reduce the number of Yamanaka factors used for reprogramming. In this way, some groups described that Oct4 expression might be sufficient to initiate and maintain the reprogramming process in early embryonic cell types or neural stem cells [7,8], while recently, Myc has been shown not to be required for the maintenance of pluripotency [9]. The adenovirus 5 early region 1 (E1) gene is involved in a large number of gene and growth regulatory activities, such as the stimulation of cell growth and the inhibition of differentiation (by deregulating the normal transcription pathways of the host cell) in order to obtain a productive infection [10]. In this E1 region, E1a is the first viral gene expressed in cells upon infection and encodes two major proteins of 289 (E1A-13S) and 243 (E1A-12S) residues that arise from differential splicing of the same transcript and differ only by the presence of a residue of 46 amino acids [11]. In addition, E1A interacts with many cellular proteins, including retinoblastoma protein (pRb), TBP, CBP/p300, p400, YY1, and CDK8, amongst others. All of these have individual contributions to the E1A function, although the interaction of E1A with chromatin remodeling proteins, such as CBP/p300 and p400, have also been suggested to be important for E1a function [12,13]. A number of studies have indicated a nexus between E1a and two of the Yamanaka factors: Oct4 and c-Myc [12–15]. The induction of c-Myc mediated by E1a is related to the binding to pRb, p300, and p400 host proteins [12,13]. Moreover, p300-binding has been shown to be essential for the transactivation of a third Yamanaka’s factor, such as Sox-2, with an indirect involvement of the E1a gene [16], and it has been reported as a key factor in the induction of S-phase and the loss of growth control [13,17]. More importantly, Oct4 transactivation is strongly stimulated by E1a in differentiated cells through the interaction with TATA box factors [14]. The ability of E1a to activate Oct4 and c-Myc in certain contexts, together with the E1a effects in histone modification patterns [18,19], led us to hypothesize that E1a overexpression alone may be sufficient to initiate the reprogramming process. Here, we demonstrate that mouse embryonic fibroblasts (MEF) can be induced into iPS-like cells, closely resembling epiblast stem cells (EpiSCs), by the presence of a single adenoviral gene, E1a-12S, although this process was maintained in combination with MEK and GSK3β small molecule inhibitors. 2. Materials and Methods 2.1. Cell Culture Murine Embryonic Fibroblasts (MEF) were obtained from HP165 mice, which have a genetic background derived from 129 and MF1 (outbred) mice crossing [20]. Wild-type MEF cells were provided by Dr. Tristan A Rodríguez (Imperial College London, London, UK), while MEF Oct4-GPF cell lines were kindly provided by Dr. Jennifer Nichols (Wellcome Trust Centre for Stem Cell Research, University of Cambridge, Cambridge, UK). All MEFs, 293T, and 293 cell lines were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM) containing 10% heat-inactivated fetal bovine serum (FBS) and 50 U penicillin/streptomycin. The media were changed twice a week. Reprogrammed MEFs were cultured under stan- dard mouse embryonic stem cells (mES) conditions: Glasgow’s modified Eagle’s medium (GMEM) containing 10% heat-inactivated FBS, 50 U penicillin/streptomycin, 1% sodium pyruvate, 1% non-essential amino acids, 0.1% β-mercaptoethanol, and 100 U of leukemia inhibitory factor (LIF) (Invitrogen, Waltham, MA, USA). mES cells were collected from E14 embryos and characterized by Dr. Tristán Rodríguez (Imperial College London, UK). mES and induced pluripotent stem (iPS)-like cells were seeded on tissue culture plates coated with 0.1% gelatin and cultured with mES standard medium supplemented with MEK (1 µM; Merck; Rahway, NJ, USA) and GSK3β (3 µM; Stemgent, Boston, NJ, USA) Cells 2023, 12, 1338 3 of 17 inhibitors [6]. Media were replaced every other day. All the experiments were performed when cells were cultured in this conditioned medium for 25–45 days. All the media and FBS used were purchased from Gibco (Waltham, MA, USA), while the other cell culture supplements were obtained from Lonza (Durham, NC, USA). All the cell lines used in this study were cultured at 37 ◦ C and 5% CO2 . 2.2. E1a Retroviral Reprogramming of MEF Oct4-GFP MEF Oct4-GFP were plated 48 h prior to infection. A total of 50,000 cells per well were seeded on a 6-well plate, previously coated with 0.1% gelatin. Polybrene (4 mg/mL) was added to the viral supernatant in order to increase the transduction efficiency. The medium was removed, and cells were incubated with 1 mL of retrovirus carrying the E1a-12S gene between 4–16 h. To prepare the retrovirus, the pLPC-E1a-12S [21] or the pLPC-GFP plasmids (kindly donated by Dr. Ramón y Cajal) were used. Maps and further explanation regarding the E1a construct could be found at the addgene site (https://www. addgene.org/18740/sequences/, accessed on 6 May 2023) or in supplemental data. Plates were centrifuged at 700× g for 45 min and 32 ◦ C. The infectious medium was removed and replaced with fresh medium. After 72 h, 50,000 reprogrammed cells were plated on feeder cells seeded on gelatinized 10 cm dishes and cultured with mES standard medium. To test GFP expression and, thus, the efficiency of reprogramming, iPS-like (GFP expressing or not) clones were visualized 14 days after transfection in a fluorescence microscopy IX81 Olympus equipped with an XC50 Olympus camera, and images were processed using CellˆD 5.1 software (Olympus, Shinjuku, Japan). Then, single clones were transferred into gelatinized 96-well flat-bottomed tissue culture plates containing 50 µL of fresh medium. Previously, clones were picked with a 10 µL micropipette from the 10 cm dishes to 96-well round-bottomed plates containing 25 µL of Trypsin/EDTA. Clones were disaggregated with trypsin, then transferred into the gelatinized 96-well flat-bottomed plates. mES standard medium was changed every day. In order to expand the clones, four gelatin-coated 48 well- plates were used per each 96 well-plate. Cells were washed with PBS, trypsinized with 50 µL of Trypsin/EDTA and 200 µL of fresh medium was added per well. Clones were disaggregated by pipetting, and 100 µL of cell suspension was transferred into a well of a 48 well-plate in duplicate. The medium was changed every day. 2.3. Alkaline Phosphatase Activity and E1a Expression Alkaline phosphatase staining was performed both in iPS-like cell cultures and in embryoid bodies with the alkaline-phosphatase detection kit (Sigma, Waltham, MA, USA) according to the manufacturer’s protocol. Briefly, cells were fixed with the citrate-acetone- formaldehyde solution for 30 s at room temperature. Then, cells were washed and stained with the alkaline staining solution for 15 min at room temperature and, after washing, with hematoxylin for 2 min. The samples were evaluated in an IX81 Olympus equipped with an XC50 Olympus camera, and images were processed using CellˆD 5.1 software (Olympus, Shinjuku, Japan). In order to evaluate whether the E1a gene was still activated in iPS-like cells, and could disrupt differentiation and embryogenesis processes, nested PCR (nPCR) and sequencing studies were performed. The detection of the E1a gene was analyzed by nPCR, as other authors described, in order to amplify the low presence of the E1a adenoviral gene in infected cells [22–24]. First, genomic DNA from 293 cells (positive control for E1a gene) and iPS-like cells was isolated with the Nucleospin Tissue extraction kit (Macherey-Nagel, Düren, Germany) following the manufacturer’s protocol. The PCR amplifications were performed in a final volume of 10 µL consisting of 1X PCR buffer (Bioline, London, UK), 1.5 mM MgCl2 (Bioline, London, UK), 0.2 mM deoxynucleoside triphosphate mix (Invit- rogen, Waltham, MA, USA), 0.3 U of BIOTAQ DNA polymerase (Bioline, London, UK), 200 nM each primer (Sigma, Waltham, MA, USA; sequences designed with Oligo 7 Software (Molecular Biology Insights Inc., Colorado Springs, CO, USA) are shown in Supplementary Table S1), and 100 ng of template DNA, in a 2720 Thermal Cycler (Applied Biosystems, Cells 2023, 12, 1338 4 of 17 Waltham, MA, USA) for a total of 35 cycles. After an initial denaturation step for 2 min at 94 ◦ C, each cycle consisted of denaturation for 20 s at 94 ◦ C, annealing for 30 s at 61 ◦ C, and primer extension for 30 s at 72 ◦ C. Then, primary PCR products were used in a second amplification. nPCR products were visualized on a 2% agarose gel stained with ethidium bromide in a G:Box UV Transilluminator (Syngene, Bangalore, India), and images were displayed by the Gen5 10.9 Data Analysis Software (Biotek, Winooski, VT, USA). The pri- mary PCR product was 383 bp, while the second product was 103 bp. Products of primary PCR were sequenced with a 3500xL Genetic Analyzer (Applied Biosystems, Waltham, MA, USA), and sequences were aligned by BioEdit v7.1.3 Software (Ibis Biosciences, Carlsbad, CA, USA) and compared to the E1a 12S region sequence from adenovirus 5 in GenBank. 2.4. Immunocytochemistry mES and iPS-like cells were seeded on gelatin-coated glass coverslips in 24-well plates at 50,000 cells/well. After 24 h, cells were fixed in 4% paraformaldehyde for 20 min at room temperature and washed thrice with PBS. In the last washing, 50 µL ammonium chloride (Panreac, Chicago, IL, USA) 1 M was added per well in order to eliminate the remaining paraformaldehyde remaining residues. Then, cells were permeabilized with 100 µL/well PBS-0.5% Triton X100 (Biorad, Hercules, CA, USA) and incubated for 10 min at room temperature. Cells were rinsed and incubated in primary antibody containing 10% FBS (Gibco, Waltham, MA, USA) in PGBA (0.1% gelatin (Sigma, Waltham, MA, USA), 1% bovine serum albumin (Sigma), and 0.05% sodium azide (Sigma, Waltham, MA, USA) in PBS) at 4 ◦ C overnight. Immunostaining was performed with the Mouse Embryonic Stem Cell Marker Panel Kit (Abcam, Cambridge, UK), which contains polyclonal rabbit anti-Oct4 (1:200), anti-Nanog (1:25), anti-Sox2 (1:50), anti-Lin 28 (1:1000), and mouse monoclonal anti-SSEA1 (1:10). Then, cells were rinsed and incubated in secondary antibody (donkey anti-rabbit or donkey anti-mouse Alexa488 (1:1000; Invitrogen, Waltham, MA, USA)) containing PGBA at room temperature for 20 min. After washing, coverslips were mounted on glass slides in DAPI-Mowiol mounting medium and subsequently sealed with nail varnish. Confocal images were collected using a Fluoview FV1000 Confocal Microscope (Olympus, Shinjuku, Japan), then processed with FV1000 Software and Adobe Photoshop SC 5.01 (Adobe Systems, San Jose, CA, USA). 2.5. Embryoid Bodies Generation mES and iPS-like cells were trypsinized and resuspended in their conditioned medium at a density of 40,000 cells/mL. Embryoid body formation was induced by seeding 50 drops of the cell suspension (1000 cells per drop) on the lid of a cell culture dish 100 mm in diameter and adding PBS to the dish. The lid was turned, and the dish was incubated at 37 ◦ C and 5% CO2 . After 48 h, cells were collected with conditioned medium and transferred to a Petri dish to allow embryoid bodies growth in suspension for 5–7 days at 37 ◦ C and 5% CO2 . Then, the embryoid bodies were transferred to 0.1% gelatin-coated dishes, where they adhered for 2–3 days. The medium was changed every 3–4 days. The samples were visualized in an IX81 Olympus equipped with an XC50 Olympus camera, and images were processed using CellˆD 5.1 software (Olympus, Shinjuku, Japan). 2.6. RNA Isolation and qPCR Analysis Total RNA was isolated from mES, iPS-like cells, MEF, and embryoid bodies with the NucleoSpin RNA II kit (Macherey-Nagel, Düren, Germany) according to the manufacturer’s protocol. Complementary DNA (cDNA) was obtained from 250 ng of total RNA with the iScript Reverse Transcription Supermix (Bio-Rad, Hercules, CA, USA) in a 2720 Thermal Cycler (Applied Biosystems, Waltham, MA, USA). Quantitative PCR (RT-qPCR) reactions of cDNA obtained from mES, iPS-like cells, and MEF were performed using 2 µL of a 2.5 ng of cDNA in a final reaction volume of 10 µL with the TaqMan Universal Master Mix II (no UNG) and different TaqMan probes in Applied Biosystems 7900HT Fast-Real Time PCR System (Applied Biosystems, Waltham, MA, USA). Pre-incubation step consisted of 1 cycle Cells 2023, 12, 1338 5 of 17 of 10 min at 95 ◦ C. The amplification step comprised 40 cycles of 15 s at 95 ◦ C and 1 min at 60 ◦ C. Then, the plate was read. cDNA samples of embryoid bodies were analyzed using an OpticonIITM DNA engine and Opticon Monitor 3.1 software (MJ Research Inc., Deltona, FL, USA). PCR reactions included SYBR Green PCR Mastermix (Qiagen, Hilden, Germany), 300 nM primers, and 2 µL of diluted cDNA template in a 30 µL reaction volume. PCR conditions were as follows: 95 ◦ C for 15 min, then 40 cycles of 94 ◦ C for 15 s, 60 ◦ C for 30 s, 72 ◦ C for 30 s, followed by plate-read. Melting curves were calculated to check the specific amplification of the sequence of interest. The relative gene expression was determined by using the 2−∆∆CT comparative method. Expression values were normalized with 18S gene values in the pluripotency genes expression assay and in the validation of microarray analyses, while β-actin was used as a housekeeping gene in the differentiation experiments. Each measurement was performed in triplicate. Data were processed with the SDS2.2.2 Software (Life Technologies, Carlsbad, CA, USA). TaqMan probes (Life Technologies, Carlsbad, CA, USA) and primer sequences (Sigma, Waltham, MA, USA) are listed in the Supplementary information, respectively. 2.7. Gene Expression Profiling MEF, mES, and iPS-like cells were harvested, RNA obtained, and cDNA transcribed as described above. Samples were hybridized onto the Whole Mouse Genome Oligo Microar- ray (Agilent Technologies, Santa Clara, CA, USA) following the manufacturer’s protocol. Briefly, samples were Cy-3 labelled (Quick-AMP Labelling Kit, Agilent Technologies, Santa Clara, CA, USA) and fragmented into pieces ranging from 35 to 200 bases. Fragmented cRNA samples (1.65 µg) were hybridized for 17 h at 65 ◦ C on chips. Then, GeneChips were washed, dried, and scanned in an Axon 5000 XL Scanner (GSI Lumonics, Bedford, MA, USA), and data were processed using Feature Extraction Software 10.0 (Agilent tech- nologies, Santa Clara, CA, USA). Microarray raw data tables have been deposited in the Gene Expression Omnibus. For statistical analysis, we selected genes whose expression differed by a factor of at least two with respect to control cells. A hierarchical clustering method was applied to group the genes and samples on the basis of the similarities in expression, and the unsupervised analyses were visualized using the Self-Organizing Tree Algorithm (SOTA) and TreeView software, assuming Euclidean distances between genes (http://bioinfo.cnio.es/cgi-bin/tools/clustering/sotarray accessed on 3 June 2016). 2.8. GeneChIP Assay Chromatin immunoprecipitation (ChIP) experiments were performed on three bio- logical replicates of MEF, mES, and iPS-like cell samples, using the HighCell# ChIP kit (Diagenode, Liege, Belgium) in accordance with the manufacturer’s instructions. Briefly, cultured cells were fixed with 1% formaldehyde for 10 min at room temperature, followed by quenching with 125 mM glycine for 5 min. This was followed by three washes with PBS and the addition of cell and nucleus lysis buffers to the cell extracts. The cells were then sonicated using a Sonics Vibra-Cell VC130 sonicator (14 × 30 s on ice with 1 min waiting on ice between pulses; Diagenode, Liege, Belgium) to shear the cross-linked chromatin into an average DNA fragment size of 200–600 bp. Immunoprecipitation was performed overnight with agitation at 4 ◦ C with 50 µg of chromatin using 5 µg of antibodies against H3K27me3 (trimethylated Lys27 of histone 3, #07-449, Millipore, Burlington, VT, USA), H3K4me3 (trimethylated Lys4 of histone 3, #003-050, Diagenode, Liege, Belgium), and Acetylated H3 (acetylated histone H3, #06-599, Millipore, Burlington, VT, USA) or unspecific rabbit IgG (#12-370, Millipore, Burlington, VT, USA) as a control. After overnight incubation, the DNA-protein-antibody complex was eluted, and the cross-links were reversed by adding elution buffer containing proteinase K followed by incubation of the samples for 4 h at 65 ◦ C. DNA was extracted by the phenol-chloroform-isoamyl alcohol, ethanol-precipitation, and resuspended in water. qPCR analysis was performed by RT-qPCR with the LC480 system (Roche, Basilea, Switzerland) with 2 µL DNA and SybrGreen master mix and the primers listed in Supplementary Table S4. The amplification program of qPCR consisted of denatu- Cells 2023, 12, 1338 6 of 17 ration at 95 ◦ C for 5 min, followed by 45 cycles at 95 ◦ C for 10 s denaturation, 60 ◦ C for 10 s annealing, and 72 ◦ C for 10 s extension. The relative proportions of immunoprecipitated promoter fragments were determined based on the threshold cycle (Ct) value for each PCR reaction. RT-PCR data analyses were obtained using the comparative Ct method using the formula: %(ChIP/Input) = 2ˆ[(Ctinput − 6.644) − CtChIP]*100 (where 6.644 is the log2 of 100 and corrects for the use of 1% input material in the qPCR determining the Ctinput). Data from each IP were quantitated in duplicate for at least three separate experiments and calculated and expressed as a percentage of their corresponding inputs (1/10 dilution) of chromatin before immunoprecipitation. 2.9. In Vivo Studies 2.9.1. Teratoma Formation All procedures were performed in accordance with the Spanish Policy for Animal Protection RD1201/05. For teratoma induction, six- to eight-week-old female BALB/c nu/nu mice (Envigo RMS Spain, Barcelona, Spain) received subcutaneous (s.c) injections of 2 × 105 mES or iPS-like cells in 200 µL of 1:10 Matrigel solution in PBS (Basement Membrane Matrix, High Concentration (HC), BD Bioscience, Franklin Lakes, NJ, USA) (n = 4/group). As described above, iPS-like cells were generated from MEFs obtained from HP165 mice [20]. When these tumors reached a volume of 100 mm3 , teratoma tissues were harvested, fixed in 4% paraformaldehyde overnight and embedded in paraffin. The differentiation into cells of the three germ layers was evaluated by hematoxylin and eosin staining and by the histopathological stainings described below. The samples were evaluated in an IX81 Olympus equipped with an XC50 Olympus camera, and images were processed using CellˆD software (Olympus, Shinjuku, Japan). 2.9.2. Chimera Production First, the karyotype of the cells was studied. On the first day, two million cells were seeded without feeders for the karyotype at 24 h and for the karyotype at 48 h. Before the karyotyping of the cells medium was changed 2 h after the medium change, 8 µl of de- mecolcine stock solution in 4 mL of medium (at final concentration 0.02 µg/mL) was added and incubated for a maximum of 3 h at 37 ◦ C and 5% CO2 . Then, cells were trypsinized and centrifuged at 1200–1400 rpm before the supernatant was aspirated. Afterwards, KCl 0.56% was added twice over the pellet mixing before incubating for 20 min at rt. Cells we fixed and washed them before assembling the slides. Finally, cells were stained with Giemsa dye. For the chromosome counting, the Ikaros program was used, counting up to 50 metaphases. Chimera production was carried out by the injection of reprogrammed cells to blasto- cysts and 8-cell embryos obtained from superovulated female mice (C57BL/6JOlaHsd) by administration of pregnant mare serum gonadotropin (PMSG), followed by the injection of human chorion gonadotropin (hCG). All blastocysts and 8-cell embryos were collected after the detection of vaginal plugs at 3.5 dpc and 2.5 dpc, respectively. Microinjected blastocysts were transferred to the uterus of pseudo-pregnant females of 2.5 dpc and 8-cell embryos to the oviduct of pseudo-pregnant females of 0.5 dpc. 2.10. Histological Studies The immunohistochemistry reactions were performed in an automated immunostain- ing platform (Discovery ULTRA, Ventana, Roche Roche, Basilea, Switzerland ). Antigen retrieval was first performed with the appropriate pH buffer (CC1 buffer), and endoge- nous peroxidase was blocked (peroxide hydrogen at 3%). Then, slides were incubated with the appropriate primary monoclonal antibodies: Actin (mouse HHF35, Dako, Santa Clara, CA, USA), NeuN (mouse A60, Millipore MAB 377), Vimentin (Rabbit D21H3, Cell signaling technology 5741), Cytokeratin, or AE1/AE3 (pankeratin) (Mouse (AE1/AE3) Thermo scientific MS-343-P0). After the primary antibody, slides were incubated with the corresponding secondary antibodies when needed (anti-mouse Abcam), and visualization Cells 2023, 12, 1338 7 of 17 systems (OmniMap anti-Rabbit, Ventana, Roche, Basilea, Switzerland) conjugated with horseradish peroxidase. An immunohistochemical reaction was developed using 3, 30-diaminobenzidine tetrahydrochloride (DAB) (ChromoMap DAB, Ventana, Roche, Basilea, Switzerland), and nuclei were counterstained with Carazzi’s hematoxylin. Finally, the slides were dehydrated, cleared, and mounted with a permanent mounting medium for microscopic evaluation. Positive control sections known to be primary antibody positive were included for each staining run. Whole slides were acquired with a slide scanner (AxioScan Z1, Zeiss, Jena, Germany), and images were captured with the Zen Blue Software (V3.1 Zeiss). 2.11. Statistical Analyses Results are reported as mean ± SEM. Statistical evaluation of data was carried out using the SPSS Statistics 17.0 software package (IBM, Armonk, NY, USA). The normal distribution of the variables was analyzed by the Kolmogorov–Smirnov test followed by the t-test or analyses of variance (ANOVA). p < 0.05 was considered to be statistically significant. 3. Results 3.1. Generation and Characterization of iPS-like Cells from MEFs by E1a-12S Overexpression To establish E1a-12S as a potential reprogramming factor, first, we tested whether we could generate iPS cells from MEFs-Oct4GFP by simple overexpression of this viral gene. A schematic overview of the methodology followed is shown in Figure 1. As control of the morphology changes and the colonies formation, the same plasmid encoding GFP has been Cells 2023, 12, x FOR PEER REVIEW 8 of 19 used for the control retroviral infections, although no colonies appeared on the previously mentioned controls (Figure S1). Figure Figure 1. Schematic 1. Schematic overview overview of E1a of E1a retroviral retroviral reprogramming reprogramming of MEF of MEF Oct4-GFP. Oct4-GFP. MEFs: MEFs: mouse mouse embryonic fibroblasts. embryonic fibroblasts. At At 14 14 days days afterinfection, after infection,the the transduced transduced cells cellsbegan begantotocluster into cluster colonies, into displayed colonies, dis- played a typical mES cell-like morphology and showed GFP expression (Figures 2aS1). a typical mES cell-like morphology and showed GFP expression (Figures 2a and andThe S1).colonies were picked The colonies to establish were picked cell cultures. to establish RecentRecent cell cultures. studiesstudies have shown the potential have shown the of E1a of potential together with Oct4 E1a together with and Oct4Klf4 and to generate Klf4 iPS colonies, to generate pointing iPS colonies, to the pointing possibility to the pos- sibility of replacing exogenous Sox2 to achieve reprogramming, though not E1a alone or E1a together with Oct4 [25]. Additionally, small molecules, such as MEK and GSK3 inhib- itors, were used to increase reprogramming efficiency and quality by preventing ESCs from differentiating, restoring cell growth, and enhancing cell viability [6,26]. Together, Cells 2023, 12, 1338 8 of 17 of replacing exogenous Sox2 to achieve reprogramming, though not E1a alone or E1a together with Oct4 [25]. Additionally, small molecules, such as MEK and GSK3 inhibitors, were used to increase reprogramming efficiency and quality by preventing ESCs from differentiating, restoring cell growth, and enhancing cell viability [6,26]. Together, these ob- servations suggested that E1a-12S was inducing some kind of cellular reprogramming, and we named these cells iPS-like. However, in order to confirm that iPS-like cells were indeed transformed by E1a-12S, immunocytochemistry, nested PCR (nPCR), and sequencing of nPCR amplification products were performed (Table S1), showing that reprogrammed cells Cells 2023, 12, x FOR PEER REVIEW 9 carried the E1a gene (Figure 2b,c). nPCR was developed in order to increase the specificity and sensitivity of PCR, as previously described for adenoviral genes [27–29]. Figure 2. Characterization of iPS-like cells of Figure 2. Characterization from MEFscells iPS-like by E1a-12S from MEFsoverexpression. (a) Bright-field (a) Brigh by E1a-12S overexpression. (left) and fluorescence (right) images of the E1a-transduced cells after 14 days of infection. (left) and fluorescence (right) images of the E1a-transduced cells after 14 days of Scale infection. Sc bar = 300 µm. (b)= Immunocytochemistry of E1A proteinof(200 300 µm. (b) Immunocytochemistry E1A× and protein 400×and inset(200× ). (c)inset PCR genotyping 400×). (c) PCR geno (right) (right) of E1a gene in of E1a gene iPS-like cellsinafter iPS-like cells after reprogramming. reprogramming. A total of 293 A total cells of 293 used were cells were as E1aused as E1 tive control. (d) Immunostaining for alkaline phosphatase on embryoid positive control. (d) Immunostaining for alkaline phosphatase on embryoid bodies (left) and iPS-like bodies (left) and iP emerging colonies (right) emerging colonies (right) (4× and inset 10×). (4× and inset 10×). After 25 days of After 25 days culture, of culture, iPS-like cells grew iPS-like stably incells the grew stably 2i culture in theand medium 2i culture clearly medium clearly developed colonies. Then, similarities between developed colonies. Then, similarities between iPS-like cells and ES cells were studied. iPS-like cells and ES cells Once in culture, studied. Once in culture, the morphology the morphology of reprogrammed of reprogrammed cells resembled more that cells resembled exerted by mor mES than that exerted of MEFs,by asmES shown than that ofS2a. in Figure MEFs, as shown Moreover, in Figure as E1a S2a. Moreover, was described to induce as E1a wa changes in the scribed cell cycleto[13,17], induce analysis changes of in the thegrowth cell cycle [13,17], abilities ofanalysis these cellsof indicated the growth abilities of that for the first 72 cells h afterindicated plating, that theirfor the first 72pattern proliferation h after plating, theirtoproliferation was similar pattern was sim mES cells. However, between 72 and mES 120 h, the cells. iPS-likebetween However, cells nearly 72 anddoubled growth cells 120 h, the iPS-like rate of mESdoubled nearly cells, the gr suggesting thatrate they maintain other characteristics to those found in the naïve of mES cells, suggesting that they maintain other characteristics to those foundpluripotent state (Figure S2b). naïveInpluripotent spite of thisstate difference, (Figurewe observed S2b). In spitethat the cell of this cycle profile difference, of the that th we observed iPS-like cells bared cycleaprofile much closer of the resemblance iPS-like cellstobaredthat of mES than a much to resemblance closer the parental MEF cellof mES th to that line (Figure S2c). the parental MEF cell line (Figure S2c). Other similaritiesOtherbetween similaritiesmES and reprogrammed between cells were cells mES and reprogrammed alsowere revealed by also revealed by alkaline phosphatase staining, which was strongly displayed in iPS-like line phosphatase staining, which was strongly displayed in iPS-like emerging co emerging colonies (Figure 2d). 2d). (Figure Furthermore, Furthermore, these cells these showed cells showed their theircapacity capacitytotogenerate generateem- embryoid b bryoid bodies(EBs) (EBs)ininsuspension suspension and in adhesion and growth in gelatin-coated and in adhesion and growth in gelatin-coated cell culture cell dishes culture dishesure (Figure S3), which S3), which were capable were capable of staining of for staining alkalineforphosphatase alkaline phosphatase as well (Figure 2d). as well (Figure 2d).used were MEFs as were used negative as negative controls, controls, and, as expected,and,EBsaswere expected, EBs were not obtained . not obtained. PEER REVIEW 10 of 19 Cells 2023, 12, 1338 9 of 17 3.2. E1a Derived iPS-like Cells Are Similar to mES Cells at the Molecular Level In order to establish the degree to which the iPS-like cells were reprogrammed, core pluripotency genes3.2. E1a Derivedwas expression iPS-like Cells Are by analyzed Similar to mES Cells real-time at the Molecular quantitative PCR Level (RT-qPCR) revealing robust expressionIn order to establish of Oct4, Sox2,theKlf4, degree to which and c-Mycthe iPS-like (Table S2,cells were3). Figure reprogrammed, In ESCs, a core specific set of transcription factors (such as Nanog, Klf4, Oct4, and Sox2) act as PCR pluripotency genes expression was analyzed by real-time quantitative part (RT-qPCR) of a revealing robust expression of Oct4, Sox2, Klf4, and c-Myc (Table S2, Figure 3). In ESCs, a pluripotent gene regulatory network (GRN) to maintain pluripotency [30–33], while c- specific set of transcription factors (such as Nanog, Klf4, Oct4, and Sox2) act as part of a Myc is able to monitor ESCs proliferation pluripotent gene regulatory and biosynthesis, network (GRN) to maintainbut no pluripotency pluripotency mainte- [30–33], while c-Myc nance and identity, iswhich able tocan be maintained monitor by the ESCs proliferation and inbiosynthesis, vitro 2i culture but no[9]. In contrast, pluripotency we maintenance found that iPS-like cells showed reduced expression of markers of the naïve state of plu-found and identity, which can be maintained by the in vitro 2i culture [9]. In contrast, we that iPS-like cells showed reduced expression of markers of the naïve state of pluripotency, ripotency, such as Nanog and Rex1, compared to mES cells (Figure 3), suggesting that such as Nanog and Rex1, compared to mES cells (Figure 3), suggesting that they had they had undergoneundergone at least partial reprogramming at least partial reprogramming to the mES to the mEScell cell state. state. Figure 3. Molecular characterization Figure 3. Molecular ofcharacterization iPS-like cells. of RT-qPCR of pluripotency iPS-like cells. genes was per- RT-qPCR of pluripotency genes was performed in mES,and formed in mES, E1a-reprogrammed, E1a-reprogrammed, and MEF cells. MEF cells. Expression valuesExpression values weretonormalized were normalized the housekeeping 18S geneto and the housekeeping 18S gene expressed related to and expressed the control related(MEF) sample to the control sample expression (MEF) expression (log(RQ) = 0, (log(RQ) = 0, where where RQ = relative quantification). ErrorRQbars = relative quantification). represent mean ± SEM Error (n =bars represent mean 3). Significant ± SEM (n = 3). differences Significant differences between markers from each sample are denoted as * iPS-mES—, # iPS-mES, between markers from each sample are denoted as * iPS-mES—-, # iPS-mES, and iPS-MEF. and & iPS-MEF. A number of previous A numberiPS studies involved of previous theinvolved iPS studies generation of only partially the generation repro-repro- of only partially grammed iPS cells (pre-iPS cells) through key intermediate grammed iPS cells (pre-iPS cells) through key intermediate steps [34], and they did steps [34], and they did not not express pluripotency markers, such as Oct4 and Nanog [35–37]. A number of typicalmark- express pluripotency markers, such as Oct4 and Nanog [35–37]. A number of typical ers of pluripotency, i.e., alkaline phosphatase or SSEA1 expression, have been shown to markers of pluripotency, i.e., alkaline mark partially phosphatase and faithfully or SSEA1 reprogrammed cells, expression, have been while Nanog expression shown was found to be to mark partially and faithfully mandatory reprogrammed in the cells, while inauguration of pluripotency in Nanog vitro andexpression in vivo ratherwas than found maintenance to be mandatory inofthe inauguration the pluripotent of pluripotency state per se [38]. in vitro and in vivo rather than As epigenetic changes maintenance of the pluripotent state per se [38]. have been demonstrated to be critical for reprogramming chromatin immunoprecipitation (ChIP), real-time RT-PCR was used to comparatively As epigenetic changes have been demonstrated to be critical for reprogramming analyze gene-specific active (H3K4me3 and H3ac) and repressive (H3K27me3) histone chromatin immunoprecipitation modification levels (ChIP), at thereal-time pluripotencyRT-PCR marker was genesused Nanog,to Oct4, comparatively and Sox2 in an- mES, iPS- alyze gene-specific active like cell(H3K4me3 lines, and MEF and(Figure H3ac) 4a,and repressive Table S2). In mES(H3K27me3) and in our histone mod- cells, reprogrammed ification levels at the pluripotency marker genes Nanog, Oct4, and Sox2 in mES, iPS-like cell lines, and MEF (Figure 4a, Table S2). In mES and in our reprogrammed cells, whereas H3K27me3 levels were low, H3K4me3 and H3Kac levels were highly abundant at the pro- moter regions of the pluripotency genes Nanog, Oct4, and Sox2. In contrast, in MEF cells, Cells 2023, 12, 1338 10 of 17 Cells 2023, 12, x FOR PEER REVIEW whereas H3K27me3 levels were low, H3K4me3 and H3Kac levels were highly abundant at 11 of 19 the promoter regions of the pluripotency genes Nanog, Oct4, and Sox2. In contrast, in MEF cells, the promoter of the three pluripotency marker genes displayed a strong enrichment for the repressive H3K27me3 modification. MEFs over-expressing E1a-12S showed epigenetic characteristics characteristics that that were weremore moresimilar similartotothose of of those ESCs ESCsthan to the than parental to the cell cell parental type.type. In- terestingly, Interestingly,a similar epigenetic a similar transformation epigenetic transformationhadhad beenbeen previously reported previously [18,19], reported sup- [18,19], porting supportingthe the involvement of this involvement adenoviral of this gene adenoviral in the gene reprogramming in the reprogrammingprocess. process. Figure 4. Expression of pluripotency in iPS-like cells. (a) Analysis of histone modification levels at β-actin β-actin (housekeeping (housekeeping gene), gene), Nanog, Nanog, Oct4, Oct4, and and Sox2 Sox2 in in MEF, MEF, iPS-like iPS-like cells, cells, and and mES. mES. The The qPCR qPCR data data are are presented as a percentage of input DNA. Data were quantitated in duplicate for at least presented as a percentage of input DNA. Data were quantitated in duplicate for at least three three separate experiments (mean ± SEM). (b) Expression of pluripotency (Nanog, Sox2, and Oct4) and separate experiments (mean ± SEM). (b) Expression of pluripotency (Nanog, Sox2, and Oct4) and embryonic (Lin28, SSEA1) related genes in iPS-like cells were revealed by immunostaining. Scale embryonic (Lin28, SSEA1) related genes in iPS-like cells were revealed by immunostaining. Scale bars = 100 µm (upper panel) and 20µm (lower panel). (c) GO analysis describing the main functions bars of the=iPS-like 100 µm cells. (upper (d)panel) andof20pluripotency-related Analysis µm (lower panel). (c) GO analysis genes containeddescribing the main functions in the microarrays showed of the iPS-like cells. (d) Analysis of pluripotency-related genes contained in the microarrays that iPS-like cells were more similar to mES cells than MEFs regarding their pluripotent state. showed that iPS-like cells were more similar to mES cells than MEFs regarding their pluripotent state. The pluripotent characteristics of IPS-like cells were also compared to mES cells by The pluripotent characteristics of IPS-like cells were also compared to mES cells immunocytochemistry. Both cell lines showed positive staining for the pluripotency by immunocytochemistry. Both cell lines showed positive staining for the pluripotency markers studied (Figure 4b), consistent with previous studies [39]. In previous reports, E1a has been shown to transcriptionally activate the expression of two of the Yamanaka factors, Oct4 and c-Myc [12–15]. The activation of Oct-4 in differentiated cells by E1a oc- curs via an interaction with TATA box factors [14]. Additionally, the E1a binding to the retinoblastoma (Rb), p300, and p400 proteins has been involved in c-Myc activation Cells 2023, 12, 1338 11 of 17 markers studied (Figure 4b), consistent with previous studies [39]. In previous reports, E1a has been shown to transcriptionally activate the expression of two of the Yamanaka factors, Oct4 and c-Myc [12–15]. The activation of Oct-4 in differentiated cells by E1a occurs via an interaction with TATA box factors [14]. Additionally, the E1a binding to the retinoblastoma (Rb), p300, and p400 proteins has been involved in c-Myc activation [12,13], leading to progression through to the S phase and the loss of growth control [13,17]. In this sense, a recent study has shown the generation of iPS mediated by the reprogramming cocktail composed of Oct4, Klf4, and E1a displaying similar results to ours regarding the endogenous expression of pluripotency molecular markers [25]. Finally, the epigenetic reprogramming induced by E1a has also been shown to be due to its binding to p300 [18,19]. In addition to these roles, the strong Sox2 and Klf4 expression observed in E1A-induced iPS-like cells indicates that this adenoviral protein can also activate, directly or indirectly, the expression of these factors. Those suggested potential mechanisms by which E1a-12S could reprogram somatic cells. Moreover, genome-wide profiling by microarray analysis showed a closer gene regulation between mES and iPS-like cells than between MEFs. At least 1860 genes were closer to mES than to MEFs when compared among them (Figures 4c and S4 and Table S4). Hierarchical clustering of microarray data identifies two major branches, one containing iPS-like and mES expression profiles and another apart containing only those of MEF (Figures 4d and S4). Particularly, iPS-like cells share a higher percentage of pluripotent genes with mES cells than with MEFs [40]. KEGG pathways (Figure S4c) from upregulated genes showed that the same pathways were activated when comparing mES and iPS-like cells vs. MEFs. On the other hand, a comparison between iPS-like cells and MEFs vs. mES cells illustrated the activation of different pathways, demonstrating a higher similarity between iPS-like and mES cells than MEFs. Hence, the genetic programs triggered by iPS-like and mES cells are more alike than those induced by MEF. Further validation by RT-qPCR of some representative genes (Il6, Lox, Loxl1, Thbs1, Vcam1) confirms this close relationship (Figure S4d). 3.3. iPS-like Cells Can Be Differentiated into Three Germ Layers In Vitro The analysis of the expression of differentiation-related genes by RT-qPCR (Table S3) in E1a-iPS derived EBs showed an upregulation in the expression of markers of all three germ layers, confirming the pluripotent nature of the reprogrammed cells (Figure S3b). Compared to control samples (mES-derived EBs), endoderm (Gata4 and Gata6) and meso- derm (Flk1 and T) related genes were slightly upregulated (<0.25 fold) in EBs generated by iPS-like cells, while ectoderm markers (Nestin, Pax6, and Sox1) were significantly upregu- lated. The expression of Nestin, Sox1, and Pax6 markers of neural and epidermal lineages was significantly higher than that observed in mES-derived EBs, most notably in the case of Pax6, which was overexpressed by about 16-fold. Finally, the in vivo development potential of iPS-like cells was tested. First, we studied teratoma formation in nude mice, and all the subcutaneous injections yielded teratomas. Haematoxylin and eosin staining of paraffin-embedded sections revealed that these cells were able to differentiate into cell types generated from the three germ layers (Figure 5a). Cells 2023, Cells 2023, 12, 12, 1338 x FOR PEER REVIEW 1312of of 19 17 Figure 5. Differentiation Differentiation potential of iPS-like cells: (a) Bright-field images of hematoxylin and eosin staining of histological staining of histological sections sections obtained obtained from from teratomas teratomas generated generated by byiPS-like iPS-likecells cells(40 (40×). ×). Arrows Arrows indicate keratinized epithelium (green), muscle (red), ciliated epithelium (yellow), nervous indicate keratinized epithelium (green), muscle (red), ciliated epithelium (yellow), nervous tissue tissue (black), and neurons (*). Black asterisk indicates the presence of neurons. (b) IHC staining of histo- (black), and neurons (*). Black asterisk indicates the presence of neurons. (b) IHC staining of logical sections obtained from teratomas generated by iPS-like cells. Images at 10× and 40× for Actin, histological sections obtained from teratomas generated by iPS-like cells. Images at 10× and 40× NeuN, Vimentin, and Cytokeratin AE1/AE3 (pankeratin). Pictures show keratinized and ciliated for Actin, NeuN, epithelium Vimentin, (CKAE1/AE3), and Cytokeratin muscle AE1/AE3 (actin), and nervous (pankeratin). tissue and neurons Pictures (NeuN)show keratinized (c) Expression of and ciliated epithelium (CKAE1/AE3), muscle (actin), and nervous tissue and neurons EpiSCs-related markers (Smad4 and Id1), epithelial marker genes (E-cadherin), and mesenchymal (NeuN) (c) Expression marker of EpiSCs-related markers (Smad4 and Id1), epithelial marker genes (E-cadherin), and genes (N-cadherin). mesenchymal marker genes (N-cadherin). Then, we tried to determine whether iPS-like cells could generate full-term chimeric mice.Then, we tried to cells Reprogrammed determine whetherinto were injected iPS-like cells could generate C57BL/6JOlaHsd full-term blastocysts, chimeric and eight cell mice. Reprogrammed cells were injected into C57BL/6JOlaHsd blastocysts, and embryos were transferred to the uterus of pseudo-pregnant females. Prior to the chimera eight cell embryos the analysis, were transferred karyotype to the of the uterus cells of pseudo-pregnant was studied females. (Figure S5). We Prior81topups, obtained the chimera and all analysis, the karyotype of the cells was studied (Figure S5). We obtained 81 of them showed uniformly black coat color, indicating the absence of chimerism from pups, and all of iPS- them showed uniformly black coat color, indicating the absence of chimerism from like cells. These data indicate that the iPS-like cells were not able to generate chimaeras, iPS-like cells. These data indicate that the iPS-like cells were not able to generate chimaeras, though though the differentiation potential of our reprogrammed cells was clearly demonstrated the differentiation potential of our reprogrammed cells was clearly demonstrated as they as they can be differentiated in cells from the three germ layers as the in vitro differentia- can be differentiated in cells from the three germ layers as the in vitro differentiation assays tion assays and the generation of teratomas revealed. With this scenario, our iPS-like cells and the generation of teratomas revealed. With this scenario, our iPS-like cells clearly clearly resemble EpiSCs, as it is shown in Figure 5b. EpiSCs are in vitro and in vivo plu- resemble EpiSCs, as it is shown in Figure 5b. EpiSCs are in vitro and in vivo pluripotent ripotent cells, though unable to contribute to chimerism, exerting a late developmental cells, though unable to contribute to chimerism, exerting a late developmental phase of phase of pluripotency [41]. This characteristic agrees with our results, as our cells showed pluripotency [41]. This characteristic agrees with our results, as our cells showed the the same behavior and expressed the key EpiSCs markers, Id1 and Smad4, and the oppo- same behavior and expressed the key EpiSCs markers, Id1 and Smad4, and the opposite site expression of the epithelial marker gene E-cadherin and the mesenchymal marker expression of the epithelial marker gene E-cadherin and the mesenchymal marker gene gene N-cadherin [42]. N-cadherin [42]. Cells 2023, 12, 1338 13 of 17 4. Discussion Reprogramming somatic cells into iPS cells can be achieved by transient forced expres- sion of a combination of the exogenous transcription factors Oct4, Sox2, Klf4, and c-Myc (OSKM). In the past decade, novel approaches for iPS generation have been developed in an effort to elucidate the molecular mechanism of the process and to in-crease the efficiency of reprogramming [43,44]. For instance, small molecules can target signaling pathways involved in the regulation of gene expression levels of pluripotent transcription factors, inducing reprogramming of somatic cells or leading to sustained pluripotency [45,46]. In this context, E1A, the first protein coding gene ex-pressed after adenovirus infection, interacts with many cellular proteins, including tumor suppressor proteins and chromatin remodeling proteins, to organize the expression of all other viral transcripts and to initiate the reprogramming of the infected cell to allow viral replication and growth [47,48]. Differ- ent studies have pointed out the direct and indirect association of E1a and the Yamanaka factors Oct4, c-Myc and Sox-2 in the regulation of the cell cycle and the repression of cellular differentiation. We observed that forced expression of E1a-12S in MEFs induced partial reprogram- ming, resulting in, what we termed, iPS-like cells with an ESC like morphology, alkaline phosphatase staining, robust Oct4, Sox2 and Klf4 expression, and an overall gene expres- sion profile that clustered closer to ESCs than MEFs. Moreover, our iPS-like cells were capable of forming colonies and generating embryoid bodies with an upregulated expres- sion of markers of all three germ layers, pointing to a clear modification of MEF cells to a pluripotent-like cell lineage. Also, when induced to form teratomas, iPS-like cells could give rise to cell types derived from the three embryonic germ layers. In addition, ChIP assays, immunocytochemistry and GEO analyses highlighted that the genetic programs triggered by iPS-like cells and mES cells are more alike than those induced by MEFs. Interestingly, a similar epigenetic transformation had been previously reported [18,19]. However, RT-qPCR experiments and microarray analysis presented low levels of Nanog and Rex1 expression, and together with the absence of contribution to chimaeras, did not point to a strong reprogramming of cells by E1a retro-viral gene. These results highlight the closer resemblance of our iPS-like cells to EpiSCs, where similar patterns are observed. Furthermore, even though two small molecule inhibitors were employed to main- tain pluripotency, the efficiency of the process was found to be lower compared to other methods [49,50]. The replacement of exogenous Sox2 by E1a has been recently shown to intervene in the reprogramming process together with Klf4 and Oct4, even though E1a alone or with Oct4 did not result in the pluripotent state [25]. Of note, the mentioned study was performed with an E1a-CR1 deleted mutant, in which direct binding to p300 [51], as well as indirect interactions with factors such as Sox-2 [16,52,53], are lacked. As we hypothesize that many of the E1a effects are due to the binding to pRb, p105 or p300, the differences between both studies might be due to the deletion on such an important region in E1a. Together with these studies, our work highlights the involvement of this adenoviral gene in the reprogramming process In summary, our study has shown that over-expression of the adenoviral protein E1a-12S in somatic cells was sufficient to induce partial reprogramming of the basal status of MEF cells, obtaining a cell state that resembles that of EpiSCs. Although E1a acts as a transcriptional regulator, controlling the expression of viral and cellular genes, the resulting partial reprogramming may be related to the use of the smaller isoform of the E1a gene (12S). The adenovirus E1a gene can be spliced into two different isoforms: 12S and 13S. The 13S isoform contains an additional protein domain called the CR3 domain, which allows the interaction with different cellular proteins, such as the tumor suppressor protein p53, whereas the 12S isoform does not. Moreover, the E1 locus presents another region called E1b. The E1b gene of adenovirus codes for a protein called early region 1B, which is important for viral replication and modulation of the host cell environment during infection. E1b has been shown to interact with several cellular proteins, including p53 or the MRN (Mre11-Rad50-Nbs1) complex, which plays a critical role in repairing double-stranded Cells 2023, 12, 1338 14 of 17 DNA breaks and maintaining telomere length [54]. Previous studies have shown that p53 plays a critical role in the reprogramming of iPS cells. During the reprogramming process, p53 can be activated by different stimuli, such as DNA damage or oxidative stress, which may induce cell cycle arrest or apoptosis to prevent the formation of iPS cells with DNA damage or chromosomal abnormalities. However, the excessive activation of p53 can also inhibit the generation of iPS cells. Therefore, the inhibition of p53 activity or the MRN complex (also, by the adenoviral CR3 or E1b proteins) may promote the generation of iPS cells with higher efficiency, as well as increase the quality of the resulting iPS cells [55,56]. Lastly, a possible explanation for the lack of chimeras would be that pRb blocking by E1a might avoid brain development on the fetuses as previously de-scribed [57]. Our findings raise important implications for the involvement of viral genes in cancer forming cells. The link between viruses and cancer has been known for decades, such as the involvement of human papiloma virus (HPV) in cervical cancer [58] or human hepatitis B virus (HBV) in hepatocellular carcinoma [59]. The E1a gene has been suspected as an oncogene since the early 80s and its neoplastic effects are most clearly demonstrated when coexpressed together with another oncogene such as Bcl2, or its counterpart E1b19k [60,61]. The fact that the molecular mechanisms underlying the generation of iPS cells are remarkably similar to those that are deregulated in cancer, to the extent that aberrant reprogramming can be directly linked to tumorigenesis [62–64], points to the possibility that at least part of the oncogenic activity of certain proteins may be directly due to their ability to activate the pluripotent gene regulatory network and in this way generating a pre-neoplastic lesion. Our results show that forced expression of E1a in differentiated cells is sufficient to induce partial reprogramming when these cells are placed under the right culture conditions. This finding provides a direct mechanistic link between viral reprogramming and the generation of cancer stem cells. Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/cells12091338/s1, Table S1: E1a nested PCR primers’ sequences; Table S2: TaqMan® Gene Expression Assays used in the detection of pluripotency gene expression in mES, iPS-like cells, and MEF, and in the validation of the microarray analyses; Table S3: qPCR primers’ sequences used in the GeneChIP assay and in the detection of differentiation markers expression in embryoid bodies (EBs); Table S4: qPCR primers’ sequences used in the GeneChIP assay and in the detection of differentiation markers expression in embryoid bodies (EBs); Table S4: Genes modified (at least 2-fold) in MEF, iPS-like, and mES cells. Figure S1: Transformation process of MEF during reprogramming; Figure S2: Characterization of iPS-like cells; Figure S3: Characterization of embryoid bodies; Figure S4: Microarray analysis of the expression of pluripotency in iPS-like cells; Figure S5: Karyotype analysis of various iPS-like cells. Supplemental Experimental Procedures: Retrovirus production, Cell proliferation assay, Cell cycle analysis, In vitro differentiation assays, Western blot. Author Contributions: Conceptualization, T.A.R., G.M. and P.M.-D.; methodology, G.M., R.G.-P., J.M.S., A.A.-C., A.P., C.B.-L. and P.M.-D.; formal analysis, G.M., R.G.-P., M.Q., G.M.-B., A.d.M., E.R., T.A.R. and P.M.-D.; data curation, G.M.-B.; writing—original draft preparation, G.M., R.G.-P. and P.M.-D.; writing—review and editing, G.M., R.G.-P. and P.M.-D.; supervision, T.A.R. and P.M.-D.; funding acquisition, T.A.R. and P.M.-D. All authors have read and agreed to the published version of the manuscript. Funding: This research was supported by Instituto de Salud Carlos III (ISCIII) (PI19/01007 and DTS21/00130) and by Fondo Europeo de Desarrollo Regional (Feder) “Una manera de hacer Europa”. We also thank CIBER-BBN, an initiative funded by the VI National R&D&i Plan 2008–2011 financed by the Instituto de Salud Carlos III (ISCIII) with the assistance of the European Regional Development Fund. This study was also partially funded by the Aragon Government (Ph.D. Grant No.r B054/12) and cofounded by Aragon/FEDER 2014–2020 “Building Europe from Aragon”. GM gratefully acknowledges the support from the Miguel Servet Program (MS19/00092; ISCIII). Institutional Review Board Statement: All procedures were performed in accordance with the Span- ish Policy for Animal Protection RD1201/05. The study was conducted according to the guidelines Cells 2023, 12, 1338 15 of 17 of the Declaration of Helsinki and approved by the Institutional Ethics Committee of University of Zaragoza (protocol code PI37/08 and date of approval 8 October). Informed Consent Statement: Not applicable. Data Availability Statement: Microarray raw data tables have been deposited in the Gene Expression Omnibus (submitter G.M.-B.). Acknowledgments: We are grateful to Carlos Parada, Jennifer Nichols, José Silva, Jesús Gil, and Fran- cisco J Quero for their ideas and scientific discussions in pluripotency, PCR, arrays, and sequencing studies. We also thank Maria Royo, Cesar Vallejo, Javier Godino, Rebeca Guerrero, Aida di Grego- rio, Alberto Cebollada, and Diana Pérez for technical assistance. The authors thank the Scientific and Technical Services at CIBA (IACS), especially tissue culture, microscopy, animal housing, flow cytometry, and pathology, and the CNIO Histopathology Core Unit for the technical support. Conflicts of Interest: The authors declare no conflict of interest. References 1. Takahashi, K.; Yamanaka, S. Induction of Pluripotent Stem Cells from Mouse Embryonic and Adult Fibroblast Cultures by Defined Factors. Cell 2006, 126, 663–676. [CrossRef] [PubMed] 2. Yu, J.; Vodyanik, M.A.; Smuga-Otto, K.; Antosiewicz-Bourget, J.; Frane, J.L.; Tian, S.; Nie, J.; Jonsdottir, G.A.; Ruotti, V.; Stewart, R. Induced pluripotent stem cell lines derived from human somatic cells. Science 2007, 318, 1917–1920. [CrossRef] [PubMed] 3. Yamanaka, S. A fresh look at iPS cells. Cell 2009, 137, 13–17. [CrossRef] [PubMed] 4. Esteban, M.A.; Wang, T.; Qin, B.; Yang, J.; Qin, D.; Cai, J.; Li, W.; Weng, Z.; Chen, J.; Ni, S. Vitamin C enhances the generation of mouse and human induced pluripotent stem cells. Cell Stem Cell 2010, 6, 71–79. [CrossRef] 5. Huangfu, D.; Osafune, K.; Maehr, R.; Guo, W.; Eijkelenboom, A.; Chen, S.; Muhlestein, W.; Melton, D. Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2. Nat. Biotechnol. 2008, 26, 1269–1275. [CrossRef] [PubMed] 6. Ying, Q.; Wray, J.; Nichols, J.; Batlle-Morera, L.; Doble, B.; Woodgett, J.; Cohen, P.; Smith, A. The ground state of embryonic stem cell self-renewal. Nature 2008, 453, 519. [CrossRef] 7. Hammachi, F.; Morrison, G.M.; Sharov, A.A.; Livigni, A.; Narayan, S.; Papapetrou, E.P.; O’Malley, J.; Kaji, K.; Ko, M.S.; Ptashne, M. Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency. Cell Rep. 2012, 1, 99–109. [CrossRef] 8. Kim, J.B.; Greber, B.; Araúzo-Bravo, M.J.; Meyer, J.; Park, K.I.; Zaehres, H.; Schöler, H.R. Direct reprogramming of human neural stem cells by OCT4. Nature 2009, 461, 649–653. [CrossRef] 9. Scognamiglio, R.; Cabezas-Wallscheid, N.; Thier, M.C.; Altamura, S.; Reyes, A.; Prendergast, Á.M.; Baumgärtner, D.; Carnevalli, L.S.; Atzberger, A.; Haas, S. Myc depletion induces a pluripotent dormant state mimicking diapause. Cell 2016, 164, 668–680. [CrossRef] 10. Lang, S.E.; Hearing, P. The adenovirus E1A oncoprotein recruits the cellular TRRAP/GCN5 histone acetyltransferase complex. Oncogene 2003, 22, 2836–2841. [CrossRef] 11. Pelka, P.; Ablack, J.N.; Fonseca, G.J.; Yousef, A.F.; Mymryk, J.S. Intrinsic structural disorder in adenovirus E1A: A viral molecular hub linking multiple diverse processes. J. Virol. 2008, 82, 7252–7263. [CrossRef] 12. Chakraborty, A.A.; Tansey, W.P. Adenoviral E1A function through Myc. Cancer Res. 2009, 69, 6–9. [CrossRef] [PubMed] 13. Singhal, G.; Leo, E.; Setty, S.K.G.; Pommier, Y.; Thimmapaya, B. Adenovirus E1A oncogene induces rereplication of cellular DNA and alters DNA replication dynamics. J. Virol. 2013, 87, 8767–8778. [CrossRef] [PubMed] 14. Schöler, H.R.; Ciesiolka, T.; Gruss, P. A nexus between Oct-4 and E1 A: Implications for gene regulation in embryonic stem cells. Cell 1991, 66, 291–304. [CrossRef] [PubMed] 15. Cartwright, P.; McLean, C.; Sheppard, A.; Rivett, D.; Jones, K.; Dalton, S. LIF/STAT3 controls ES cell self-renewal and pluripotency by a Myc-dependent mechanism. Development 2005, 132, 885–896. [CrossRef] 16. Nowling, T.K.; Johnson, L.R.; Wiebe, M.S.; Rizzino, A. Identification of the transactivation domain of the transcription factor Sox-2 and an associated co-activator. J. Biol. Chem. 2000, 275, 3810–3818. [CrossRef] 17. Kadeppagari, R.-K.; Sankar, N.; Thimmapaya, B. Adenovirus transforming protein E1A induces c-Myc in quiescent cells by a novel mechanism. J. Virol. 2009, 83, 4810–4822. [CrossRef] 18. Ferrari, R.; Pellegrini, M.; Horwitz, G.A.; Xie, W.; Berk, A.J.; Kurdistani, S.K. Epigenetic reprogramming by adenovirus e1a. Science 2008, 321, 1086–1088. [CrossRef] 19. Horwitz, G.A.; Zhang, K.; McBrian, M.A.; Grunstein, M.; Kurdistani, S.K.; Berk, A.J. Adenovirus small e1a alters global patterns of histone modification. Science 2008, 321, 1084–1085. [CrossRef] 20. Ying, Q.-L.; Nichols, J.; Evans, E.P.; Smith, A.G. Changing potency by spontaneous fusion. Nature 2002, 416, 545–548. [CrossRef] 21. Samuelson, A.V.; Lowe, S.W. Selective induction of p53 and chemosensitivity in RB-deficient cells by E1A mutants unable to bind the RB-related proteins. Proc. Natl. Acad. Sci. USA 1997, 94, 12094–12099. [CrossRef] [PubMed] Cells 2023, 12, 1338 16 of 17 22. Gustafsson, B.; Huang, W.; Bogdanovic, G.; Gauffin, F.; Nordgren, A.; Talekar, G.; Ornelles, D.; Gooding, L. Adenovirus DNA is detected at increased frequency in Guthrie cards from children who develop acute lymphoblastic leukaemia. Br. J. Cancer 2007, 97, 992–994. [CrossRef] [PubMed] 23. Honkaniemi, E.; Talekar, G.; Huang, W.; Bogdanovic, G.; Forestier, E.; Von Doblen, U.; Engvall, M.; Ornelles, D.; Gooding, L.; Gustafsson, B. Adenovirus DNA in Guthrie cards from children who develop acute lymphoblastic leukaemia (ALL). Br. J. Cancer 2010, 102, 796–798. [CrossRef] [PubMed] 24. Vasconcelos, G.; Kang, M.; Pombo-de-Oliveira, M.; Schiffman, J.; Lorey, F.; Buffler, P.; Wiemels, J. Adenovirus detection in Guthrie cards from paediatric leukaemia cases and controls. Br. J. Cancer 2008, 99, 1668–1672. [CrossRef] 25. Marthaler, A.G.; Adachi, K.; Tiemann, U.; Wu, G.; Sabour, D.; Velychko, S.; Kleiter, I.; Schöler, H.R.; Tapia, N. Enhanced OCT4 transcriptional activity substitutes for exogenous SOX2 in cellular reprogramming. Sci. Rep. 2016, 6, 19415. [CrossRef] 26. Zhang, R.; Zhang, L.-h.; Xie, X. iPSCs and small molecules: A reciprocal effort towards better approaches for drug discovery. Acta Pharmacol. Sin. 2013, 34, 765–776. [CrossRef] 27. Haeussler, D.J.; Evangelista, A.M.; Burgoyne, J.R.; Cohen, R.A.; Bachschmid, M.M.; Pimental, D.R. Checkpoints in adenoviral production: Cross-contamination and E1A. PLoS ONE 2011, 6, e23160. [CrossRef] 28. Kuwano, K.; Nomoto, Y.; Kunitake, R.; Hagimoto, N.; Matsuba, T.; Nakanishi, Y.; Hara, N. Detection of adenovirus E1A DNA in pulmonary fibrosis using nested polymerase chain reaction. Eur. Respir. J. 1997, 10, 1445–1449. [CrossRef] 29. Lavine, J.A.; Raess, P.W.; Davis, D.B.; Rabaglia, M.E.; Presley, B.K.; Keller, M.P.; Beinfeld, M.C.; Kopin, A.S.; Newgard, C.B.; Attie, A.D. Contamination with E1A-positive wild-type adenovirus accounts for species-specific stimulation of islet cell proliferation by CCK: A cautionary note. Mol. Endocrinol. 2010, 24, 464–467. [CrossRef] 30. Chambers, I.; Colby, D.; Robertson, M.; Nichols, J.; Lee, S.; Tweedie, S.; Smith, A. Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells. Cell 2003, 113, 643–655. [CrossRef] 31. Golan-Mashiach, M.; Dazard, J.-E.; Gerecht-Nir, S.; Amariglio, N.; Fisher, T.; Jacob-Hirsch, J.; Bielorai, B.; Osenberg, S.; Barad, O.; Getz, G. Design principle of gene expression used by human stem cells: Implication for pluripotency. FASEB J. 2005, 19, 147–149. [CrossRef] [PubMed] 32. Mitsui, K.; Tokuzawa, Y.; Itoh, H.; Segawa, K.; Murakami, M.; Takahashi, K.; Maruyama, M.; Maeda, M.; Yamanaka, S. The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells. Cell 2003, 113, 631–642. [CrossRef] 33. Picanço-Castro, V.; Russo-Carbolante, E.; Covas, D.T. Forced expression of Nanog in human bone marrow-derived endothelial cells activates other six pluripotent genes. Cell. Reprogramming (Former. Cloning Stem Cells) 2012, 14, 187–192. [CrossRef] 34. O’Malley, J.; Skylaki, S.; Iwabuchi, K.A.; Chantzoura, E.; Ruetz, T.; Johnsson, A.; Tomlinson, S.R.; Linnarsson, S.; Kaji, K. High-resolution analysis with novel cell-surface markers identifies routes to iPS cells. Nature 2013, 499, 88–91. [CrossRef] [PubMed] 35. Mikkelsen, T.S.; Hanna, J.; Zhang, X.; Ku, M.; Wernig, M.; Schorderet, P.; Bernstein, B.E.; Jaenisch, R.; Lander, E.S.; Meissner, A. Dissecting direct reprogramming through integrative genomic analysis. Nature 2008, 454, 49–55. [CrossRef] [PubMed] 36. Plath, K.; Lowry, W.E. Progress in understanding reprogramming to the induced pluripotent state. Nat. Rev. Genet. 2011, 12, 253–265. [CrossRef] 37. Silva, J.; Barmndon, O.; Nichols, J.; Kawagnchi, l.; Theunisscn, T.; Smith, A. Promotion of reprogramming to ground state pluripotency by signal inhibition. PLoS Biol. 2008, 6, e253. [CrossRef] 38. Dejosez, M.; Zwaka, T.P. Pluripotency and nuclear reprogramming. Annu. Rev. Biochem. 2012, 81, 737–765. [CrossRef] 39. Brons, I.G.M.; Smithers, L.E.; Trotter, M.W.; Rugg-Gunn, P.; Sun, B.; Chuva de Sousa Lopes, S.M.; Howlett, S.K.; Clarkson, A.; Ahrlund-Richter, L.; Pedersen, R.A. Derivation of pluripotent epiblast stem cells from mammalian embryos. Nature 2007, 448, 191–195. [CrossRef] 40. Mallon, B.S.; Chenoweth, J.G.; Johnson, K.R.; Hamilton, R.S.; Tesar, P.J.; Yavatkar, A.S.; Tyson, L.J.; Park, K.; Chen, K.G.; Fann, Y.C. StemCellDB: The human pluripotent stem cell database at the National Institutes of Health. Stem Cell Res. 2013, 10, 57–66. [CrossRef] 41. Zhou, H.; Li, W.; Zhu, S.; Joo, J.Y.; Do, J.T.; Xiong, W.; Kim, J.B.; Zhang, K.; Schöler, H.R.; Ding, S. Conversion of mouse epiblast stem cells to an earlier pluripotency state by small molecules. J. Biol. Chem. 2010, 285, 29676–29680. [CrossRef] [PubMed] 42. Song, L.; Chen, J.; Peng, G.; Tang, K.; Jing, N. Dynamic Heterogeneity of Brachyury in Mouse Epiblast Stem Cells Mediates Distinct Response to Extrinsic Bone Morphogenetic Protein (BMP) Signaling. J. Biol. Chem. 2016, 291, 15212–15225. [CrossRef] [PubMed] 43. Schmidt, R.; Plath, K. The roles of the reprogramming factors Oct4, Sox2 and Klf4 in resetting the somatic cell epigenome during induced pluripotent stem cell generation. Genome Biol. 2012, 13, 251. [CrossRef] 44. Teshigawara, R.; Cho, J.; Kameda, M.; Tada, T. Mechanism of human somatic reprogramming to iPS cell. Lab. Investig. 2017, 97, 1152–1157. [CrossRef] 45. Higuchi, A.; Ling, Q.-D.; Kumar, S.S.; Munusamy, M.A.; Alarfaj, A.A.; Chang, Y.; Kao, S.-H.; Lin, K.-C.; Wang, H.-C.; Umezawa, A. Generation of pluripotent stem cells without the use of genetic material. Lab. Investig. 2015, 95, 26–42. [CrossRef] [PubMed] 46. Lin, T.; Wu, S. Reprogramming with small molecules instead of exogenous transcription factors. Stem Cells Int. 2015, 2015, 794632. [CrossRef] Cells 2023, 12, 1338 17 of 17 47. Costa, R.; Akkerman, N.; Graves, D.; Crisostomo, L.; Bachus, S.; Pelka, P. Characterization of adenovirus 5 E1A exon 1 deletion mutants in the viral replicative cycle. Viruses 2020, 12, 213. [CrossRef] 48. Zemke, N.R.; Gou, D.; Berk, A.J. Dedifferentiation by adenovirus E1A due to inactivation of Hippo pathway effectors YAP and TAZ. Genes Dev. 2019, 33, 828–843. [CrossRef] 49. Hu, K. All roads lead to induced pluripotent stem cells: The technologies of iPSC generation. Stem Cells Dev. 2014, 23, 1285–1300. [CrossRef] 50. Kelaini, S.; Cochrane, A.; Margariti, A. Direct reprogramming of adult cells: Avoiding the pluripotent state. Stem Cells Cloning Adv. Appl. 2014, 7, 19. 51. Pelka, P.; Ablack, J.N.; Torchia, J.; Turnell, A.S.; Grand, R.J.; Mymryk, J.S. Transcriptional control by adenovirus E1A conserved region 3 via p300/CBP. Nucleic Acids Res. 2009, 37, 1095–1106. [CrossRef] [PubMed] 52. Dai, X.; Liu, P.; Lau, A.W.; Liu, Y.; Inuzuka, H. Acetylation-dependent regulation of essential iPS-inducing factors: A regulatory crossroad for pluripotency and tumorigenesis. Cancer Med. 2014, 3, 1211–1224. [CrossRef] [PubMed] 53. Nowling, T.; Bernadt, C.; Johnson, L.; Desler, M.; Rizzino, A. The Co-activator p300 Associates Physically with and Can Mediate the Action of the Distal Enhancer of the FGF-4 gene. J. Biol. Chem. 2003, 278, 13696–13705. [CrossRef] [PubMed] 54. Berk, A.J. Recent lessons in gene expression, cell cycle control, and cell biology from adenovirus. Oncogene 2005, 24, 7673–7685. [CrossRef] 55. Lin, T.; Lin, Y. p53 switches off pluripotency on differentiation. Stem Cell Res. Ther. 2017, 8, 44. [CrossRef] [PubMed] 56. Volman, Y.; Hefetz, R.; Galun, E.; Rachmilewitz, J. DNA damage alters EGFR signaling and reprograms cellular response via Mre-11. Sci. Rep. 2022, 12, 5760. [CrossRef] 57. Missero, C.; Serra, C.; Stenn, K.; Dotto, G.P. Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation. J. Cell Biol. 1993, 121, 1109–1120. [CrossRef] 58. Walboomers, J.M.; Jacobs, M.V.; Manos, M.M.; Bosch, F.X.; Kummer, J.A.; Shah, K.V.; Snijders, P.J.; Peto, J.; Meijer, C.J.; Muñoz, N. Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J. Pathol. 1999, 189, 12–19. [CrossRef] 59. Brechot, C.; Pourcel, C.; Louise, A.; Rain, B.; Tiollais, P. Presence of integrated hepatitis B virus DNA sequences in cellular DNA of human hepatocellular carcinoma. Nature 1980, 286, 533–535. [CrossRef] 60. Boulakia, C.A.; Chen, G.; Ng, F.W.; Teodoro, J.G.; Branton, P.E.; Nicholson, D.W.; Poirier, G.G.; Shore, G.C. Bcl-2 and adenovirus E1B 19 kDA protein prevent E1A-induced processing of CPP32 and cleavage of poly(ADP-ribose) polymerase. Oncogene 1996, 12, 529–535. 61. Chiou, S.-K.; Tseng, C.-C.; Rao, L.; White, E. Functional complementation of the adenovirus E1B 19-kilodalton protein with Bcl-2 in the inhibition of apoptosis in infected cells. J. Virol. 1994, 68, 6553–6566. [CrossRef] [PubMed] 62. Slack, R.S.; El-Bizri, H.; Wong, J.; Belliveau, D.J.; Miller, F.D. A critical temporal requirement for the retinoblastoma protein family during neuronal determination. J. Cell Biol. 1998, 140, 1497–1509. [CrossRef] 63. Goding, C.R.; Pei, D.; Lu, X. Cancer: Pathological nuclear reprogramming? Nat. Rev. Cancer 2014, 14, 568–573. [CrossRef] [PubMed] 64. Trosko, J.E. Induction of iPS cells and of cancer stem cells: The stem cell or reprogramming hypothesis of cancer? Anat. Rec. 2014, 297, 161–173. [CrossRef] [PubMed] Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). 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