Elisa Giacomelli, Milena Bellin, Valeria V. Orlova, Christine L. Mummery
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Abstract
The formation of cardiac mesodermal subtypes is highly regulated in time and space during heart development. In vitro models based on human pluripotent stem cells (hPS cells) provide opportunities to study mechanisms underlying fate choices governing lineage specification from common cardiovascular progenitors in human embryos. The generation of cardiac endothelial cells in particular allows the creation of complex models of cardiovascular disorders in which either cardiomyocytes or endothelial cells are affected. Here, a protocol for co-differentiation of cardiomyocytes and endothelial cells from cardiac mesoderm using hPS cells is described. Precise details for the enrichment of each cell population from heterogeneous-differentiated cultures, a description of how to maintain and dissociate enriched cardiomyocytes, and the expansion and cryopreservation of enriched endothelial cells are all provided. The generation and culture of three-dimensional cardiac microtissues from these cell populations is described and guidelines for the characterization of microtissues by immunofluorescent staining and re-plating for downstream applications are provided. © 2017 by John Wiley & Sons, Inc.
人类多能干细胞来源的心肌细胞和心脏中胚层内皮细胞的共分化提供了心脏显微组织的三维模型
心脏中胚层亚型的形成在时间和空间上受到高度调控。基于人类多能干细胞(hPS细胞)的体外模型为研究人类胚胎中常见心血管祖细胞的谱系规范的命运选择机制提供了机会。心脏内皮细胞的产生尤其允许创建心血管疾病的复杂模型,其中心肌细胞或内皮细胞受到影响。本文描述了一种利用hPS细胞从心脏中胚层共分化心肌细胞和内皮细胞的方法。从异质分化培养中富集每个细胞群的精确细节,描述如何维持和分离富集的心肌细胞,以及扩增和冷冻保存富集的内皮细胞都提供了。描述了从这些细胞群中产生和培养三维心脏微组织,并提供了通过免疫荧光染色和下游应用重新电镀表征微组织的指南。©2017 by John Wiley &儿子,Inc。
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