Differentiation, Evaluation, and Application of Human Induced Pluripotent Stem Cell–Derived Endothelial Cells

dc.contributor.authorLin, Yang
dc.contributor.authorGil, Chang-Hyun
dc.contributor.authorYoder, Mervin C.
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2018-06-29T13:44:36Z
dc.date.available2018-06-29T13:44:36Z
dc.date.issued2017-11
dc.description.abstractThe emergence of induced pluripotent stem cell (iPSC) technology paves the way to generate large numbers of patient-specific endothelial cells (ECs) that can be potentially delivered for regenerative medicine in patients with cardiovascular disease. In the last decade, numerous protocols that differentiate EC from iPSC have been developed by many groups. In this review, we will discuss several common strategies that have been optimized for human iPSC-EC differentiation and subsequent studies that have evaluated the potential of human iPSC-EC as a cell therapy or as a tool in disease modeling. In addition, we will emphasize the importance of using in vivo vessel-forming ability and in vitro clonogenic colony–forming potential as a gold standard with which to evaluate the quality of human iPSC-EC derived from various protocols.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationLin, Y., Gil, C.-H., & Yoder, M. C. (2017). Differentiation, Evaluation, and Application of Human Induced Pluripotent Stem Cell–Derived Endothelial Cells. Arteriosclerosis, Thrombosis, and Vascular Biology, 37(11), 2014–2025. https://doi.org/10.1161/ATVBAHA.117.309962en_US
dc.identifier.urihttps://hdl.handle.net/1805/16601
dc.language.isoenen_US
dc.publisherAHAen_US
dc.relation.isversionof10.1161/ATVBAHA.117.309962en_US
dc.relation.journalArteriosclerosis, Thrombosis, and Vascular Biologyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectcardiovascular diseasesen_US
dc.subjectendothelial cellsen_US
dc.subjectcell therapyen_US
dc.titleDifferentiation, Evaluation, and Application of Human Induced Pluripotent Stem Cell–Derived Endothelial Cellsen_US
dc.typeArticleen_US
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