4.4 Article

Directed Differentiation of Hemogenic Endothelial Cells from Human Pluripotent Stem Cells

期刊

出版社

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/62391

关键词

-

资金

  1. NIH [HL128064, U2EB017103]
  2. CT Innovations [15-RMB-YALE-04]

向作者/读者索取更多资源

Blood vessels are crucial components in all tissues of the body, with diverse functions, and deriving hemogenic endothelial cells from human pluripotent stem cells offers potential for studying endothelial-to-hematopoietic transition and therapeutic applications. A novel differentiation protocol presented here allows for the generation of well-defined hemogenic endothelial cells from human embryonic stem cells in a short timeframe, providing opportunities for further molecular studies and potential therapeutic applications.
Blood vessels are ubiquitously distributed within all tissues of the body and perform diverse functions. Thus, derivation of mature vascular endothelial cells, which line blood vessel lumens, from human pluripotent stem cells is crucial for a multitude of tissue engineering and regeneration applications. In vivo, primordial endothelial cells are derived from the mesodermal lineage and are specified toward specific subtypes, including arterial, venous, capillary, hemogenic, and lymphatic. Hemogenic endothelial cells are of particular interest because, during development, they give rise to hematopoietic stem and progenitor cells, which then generate all blood lineages throughout life. Thus, creating a system to generate hemogenic endothelial cells in vitro would provide an opportunity to study endothelial-to-hematopoietic transition, and may lead to ex vivo production of human blood products and reduced reliance on human donors. While several protocols exist for the derivation of progenitor and primordial endothelial cells, generation of well-characterized hemogenic endothelial cells from human stem cells has not been described. Here, a method for the derivation of hemogenic endothelial cells from human embryonic stem cells in approximately 1 week is presented: a differentiation protocol with primitive streak cells formed in response to GSK3 beta inhibitor (CHIR99021), then mesoderm lineage induction mediated by bFGF, followed by primordial endothelial cell development promoted by BMP4 and VEGF-A, and finally hemogenic endothelial cell specification induced by retinoic acid. This protocol yields a well-defined population of hemogenic endothelial cells that can be used to further understand their molecular regulation and endothelial-to-hematopoietic transition, which has the potential to be applied to downstream therapeutic applications.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据