Human induced pluripotent stem cell-derived cardiac myocytes and sympathetic neurons in disease modelling
Li, Ni (University of Oxford)
Edel, Michael J (Universitat Autònoma de Barcelona)
Liu, Kun (Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence)
Denning, Chris (University of Nottingham)
Betts, Jacob (Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence)
Neely, Oliver C. (Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence)
Li, Dan (Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence)
Paterson, David J. (Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence)

Fecha:	2023
Resumen:	Human induced pluripotent stem cells (hiPSC) offer an unprecedented opportunity to generate model systems that facilitate a mechanistic understanding of human disease. Current differentiation protocols are capable of generating cardiac myocytes (hiPSC-CM) and sympathetic neurons (hiPSC-SN). However, the ability of hiPSC-derived neurocardiac co-culture systems to replicate the human phenotype in disease modelling is still in its infancy. Here, we adapted current methods for efficient and replicable induction of hiPSC-CM and hiPSC-SN. Expression of cell-type-specific proteins were confirmed by flow cytometry and immunofluorescence staining. The utility of healthy hiPSC-CM was tested with pressor agents to develop a model of cardiac hypertrophy. Treatment with angiotensin II (AngII) resulted in: (i) cell and nuclear enlargement, (ii) enhanced fetal gene expression, and (iii) FRET-activated cAMP responses to adrenergic stimulation. AngII or KCl increased intracellular calcium transients in hiPSC-SN. Immunostaining in neurocardiac co-cultures demonstrated anatomical innervation to myocytes, where myocyte cytosolic cAMP responses were enhanced by forskolin compared with monocultures. In conclusion, human iPSC-derived cardiac myocytes and sympathetic neurons replicated many features of the anatomy and (patho)physiology of these cells, where co-culture preparations behaved in a manner that mimicked key physiological responses seen in other mammalian systems. This article is part of the theme issue 'The heartbeat: its molecular basis and physiological mechanisms'.
Derechos:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.
Lengua:	Anglès
Documento:	Article ; recerca ; Versió publicada
Materia:	Cardiac myocytes ; Hipsc ; Neurocardiac co-culture ; Sympathetic neurons
Publicado en:	Philosophical Transactions of the Royal Society B: Biological Sciences, Vol. 378 (june 2023) , ISSN 1471-2970

DOI: 10.1098/rstb.2022.0173
PMID: 37122212

10 p, 896.7 KB

El registro aparece en las colecciones:
Artículos > Artículos de investigación
Artículos > Artículos publicados