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Human Induced Pluripotent Stem Cell-Derived Vascular Cells: Recent Progress and Future Directions

Authors
 Jee Eun Oh  ;  Cholomi Jung  ;  Young-Sup Yoon 
Citation
 JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE, Vol.8(11) : 148, 2021-11 
Journal Title
JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE
Issue Date
2021-11
Keywords
cardiovascular disease ; endothelial cell ; human induced pluripotent stem cell ; regenerative medicine ; smooth muscle cell ; stem cell
Abstract
Human induced pluripotent stem cells (hiPSCs) hold great promise for cardiovascular regeneration following ischemic injury. Considerable effort has been made toward the development and optimization of methods to differentiate hiPSCs into vascular cells, such as endothelial and smooth muscle cells (ECs and SMCs). In particular, hiPSC-derived ECs have shown robust potential for promoting neovascularization in animal models of cardiovascular diseases, potentially achieving significant and sustained therapeutic benefits. However, the use of hiPSC-derived SMCs that possess high therapeutic relevance is a relatively new area of investigation, still in the earlier investigational stages. In this review, we first discuss different methodologies to derive vascular cells from hiPSCs with a particular emphasis on the role of key developmental signals. Furthermore, we propose a standardized framework for assessing and defining the EC and SMC identity that might be suitable for inducing tissue repair and regeneration. We then highlight the regenerative effects of hiPSC-derived vascular cells on animal models of myocardial infarction and hindlimb ischemia. Finally, we address several obstacles that need to be overcome to fully implement the use of hiPSC-derived vascular cells for clinical application.
Files in This Item:
T999202317.pdf Download
DOI
10.3390/jcdd8110148
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Yoon, Young Sup(윤영섭)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/190712
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