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Healthy cardiac myocytes can decrease sympathetic hyperexcitability in the early stages of hypertension

Abstract:
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'
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fnsyn.2022.949150
Publication website:
https://ddd.uab.cat/pub/artpub/2023/pmc_10150199/pmc_10150199.pdf

Authors

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-2225-4020
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-4603-9376
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-3906-4066
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-2230-9300
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-7399-3256


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Funder identifier:
10.13039/501100000274


Publisher:
Frontiers Media
Journal:
Frontiers in Synaptic Neuroscience More from this journal
Volume:
14
Pages:
949150-949150
Article number:
949150
Publication date:
2022-08-04
DOI:
EISSN:
1663-3563
ISSN:
1663-3563


Language:
English
Keywords:
Pubs id:
1275290
Local pid:
pubs:1275290
Source identifiers:
W4289745143
Deposit date:
2026-04-28
ARK identifier:
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