Journal article
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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(Preview, Version of record, pdf, 2.7MB, Terms of use)
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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
- 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:
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1663-3563
- ISSN:
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1663-3563
- Language:
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English
- Keywords:
- Pubs id:
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1275290
- Local pid:
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pubs:1275290
- Source identifiers:
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W4289745143
- Deposit date:
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2026-04-28
- ARK identifier:
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Terms of use
- Copyright date:
- 2022
- Licence:
- CC Attribution (CC BY)
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