Protocol to generate cardiac pericytes from human induced pluripotent stem cells
Cardiac pericytes are a critical yet enigmatic cell type within the coronary microvasculature. Since primary human cardiac pericytes are not readily accessible, we present a protocol to generate them from human induced pluripotent stem cells (hiPSCs). Our protocol involves several steps, including t...
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Veröffentlicht in: | STAR protocols 2023-06, Vol.4 (2), p.102256-102256, Article 102256 |
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Zusammenfassung: | Cardiac pericytes are a critical yet enigmatic cell type within the coronary microvasculature. Since primary human cardiac pericytes are not readily accessible, we present a protocol to generate them from human induced pluripotent stem cells (hiPSCs). Our protocol involves several steps, including the generation of intermediate cell types such as mid-primitive streak, lateral plate mesoderm, splanchnic mesoderm, septum transversum, and epicardium, before deriving cardiac pericytes. With hiPSC-derived cardiac pericytes, researchers can decipher the mechanisms underlying coronary microvascular dysfunction.
For complete details on the use and execution of this protocol, please refer to Shen et al.1
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•A 7-stage stepwise protocol to generate hiPSC-derived epicardial cells•Highly efficient differentiation of epicardial cells into cardiac pericytes•Derived cardiac pericytes exhibit typical morphology, gene markers, and cell functions
Cardiac pericytes are a critical yet enigmatic cell type within the coronary microvasculature. Since primary human cardiac pericytes are not readily accessible, we present a protocol to generate them from human induced pluripotent stem cells (hiPSCs). Our protocol involves several steps, including the generation of intermediate cell types such as mid-primitive streak, lateral plate mesoderm, splanchnic mesoderm, septum transversum, and epicardium, before deriving cardiac pericytes. With hiPSC-derived cardiac pericytes, researchers can decipher the mechanisms underlying coronary microvascular dysfunction. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2023.102256 |