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Destination: mk:title Children: Item: Title: 1 Introduction Destination: mk:H1_1 Item: Title: 2 Materials and methods Destination: mk:H1_2 Children: Item: Title: 2.1 Porcine cardiac adipose tissue-derived MSC isolation and culture Destination: mk:H2_1 Item: Title: 2.2 Extracellular vesicle production and isolation Destination: mk:H2_2 Item: Title: 2.3 Bead-based flow cytometry Destination: mk:H2_3 Item: Title: 2.4 Cryo-electron microscopy Destination: mk:H2_4 Item: Title: 2.5 Nanoparticle tracking analysis Destination: mk:H2_5 Item: Title: 2.6 EV staining Destination: mk:H2_6 Item: Title: 2.7 Endotoxin detection Destination: mk:H2_7 Item: Title: 2.8 Porcine peripheral blood mononuclear cells isolation and functional assays Destination: mk:H2_8 Item: Title: 2.9 Cytokine response Destination: mk:H2_9 Item: Title: 2.10 Porcine outgrowing endothelial progenitor cell cultures and characterization Destination: mk:H2_10 Item: Title: 2.11 Migration assay Destination: mk:H2_11 Item: Title: 2.12 Tube formation assay Destination: mk:H2_12 Item: Title: 2.13 Generation of cardiac scaffolds Destination: mk:H2_13 Item: Title: 2.14 EV delivery into decellularised scaffolds Destination: mk:H2_14 Item: Title: 2.15 Near-infrared scaffold scanning Destination: mk:H2_15 Item: Title: 2.16 Scanning electron microscopy Destination: mk:H2_16 Item: Title: 2.17 Myocardial infarction pig model Destination: mk:H2_17 Item: Title: 2.18 Tissue collection, morphometric and histopathological analyses Destination: mk:H2_18 Item: Title: 2.19 Immunohistochemical analysis Destination: mk:H2_19 Item: Title: 2.20 Statistical analysis Destination: mk:H2_20 Item: Title: 3 Results Destination: mk:H1_3 Children: Item: Title: 3.1 Porcine cATMSC-EV purification Destination: mk:H2_21 Item: Title: 3.2 cATMSC-EV have immune suppressive properties Destination: mk:H2_22 Item: Title: 3.3 Porcine cATMSC-EV recruit allogeneic pro-regenerative cells and promote angiogenesis Destination: mk:H2_23 Item: Title: 3.4 Biocompatible 3D-Engineered scaffolds maintain the internal ultrastructure and are devoid of cells after decellularisation Destination: mk:H2_24 Item: Title: 3.5 Porcine cATMSC-EV are successfully retained within 3D-Engineered cardiac scaffolds Destination: mk:H2_25 Item: Title: 3.6 Porcine cATMSC-EV combined with cardiac scaffolds abrogate the cytokine response of allogeneic PBMC Destination: mk:H2_26 Item: Title: 3.7 Locally administered porcine cATMSC-EV stay within scaffolds and infarct core Destination: mk:H2_27 Item: Title: 3.8 In vivo scaffold neovascularization and reduction of macrophage and T cell infiltration Destination: mk:H2_28 Item: Title: 4 Discussion Destination: mk:H1_4 Item: Title: Funding sources Destination: mk:H1_5 Item: Title: CRediT authorship contribution statement Destination: mk:H1_6 Item: Title: Declaration of competing interest Destination: creditlink4 Item: Title: Acknowledgements Destination: mk:HH1_5 Item: Title: Abbreviations Destination: mk:H1_7 Item: 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XMP: application/pdf 10.1016/j.bioactmat.2021.02.026 KeAi Communications Co., Ltd Bioactive Materials, 6 (2021) 3314-3327. doi:10.1016/j.bioactmat.2021.02.026 Exosomes Mesenchymal stem/stromal cells Migration Infiltration Cardiac tissue engineering Local administration of porcine immunomodulatory, chemotactic and angiogenic extracellular vesicles using engineered cardiac scaffolds for myocardial infarction Marta Monguió-Tortajada Cristina Prat-Vidal Miriam Moron-Font Marta Clos-Sansalvador Alexandra Calle Paloma Gastelurrutia Adriana Cserkoova Anna Morancho Miguel Ángel Ramírez Anna Rosell Antoni Bayes-Genis Carolina Gálvez-Montón Francesc E. Borràs Santiago Roura journal Bioactive Materials © 2021 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. 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