Protocol for differentiating hematopoietic progenitor cells from human pluripotent stem cells in chemically defined monolayer culture.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Shaokang Mo, Kengyuan Qu, Jun Shen, Kuangyu Yen
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引用次数: 0

Abstract

Human pluripotent stem cells (hPSCs) provide a powerful platform for generating hematopoietic progenitor cells (HPCs) and investigating hematopoietic development. Here, we present a protocol for maintaining hPSCs and inducing their differentiation into HPCs through the endothelial-to-hematopoietic transition (EHT) on vitronectin-coated plates. We outline steps for evaluating the efficiency of HPC generation and assessing their potential to differentiate into various hematopoietic lineages. This protocol serves as a framework for exploring human hematopoiesis and generating various functional blood cells. For complete details on the use and execution of this protocol, please refer to Shen et al.1 and Qu et al.2.

在化学定义的单层培养中从人多能干细胞中分化造血祖细胞的方法。
人多能干细胞(Human pluripotent stem cells, hPSCs)为造血祖细胞(hematopotic progenitor cells, HPCs)的生成和研究造血发育提供了一个强大的平台。在这里,我们提出了一种在体外连接蛋白涂层板上通过内皮-造血转化(EHT)维持人造血干细胞并诱导其分化为人造血干细胞的方案。我们概述了评估HPC生成效率和评估其分化为各种造血谱系的潜力的步骤。该方案可作为探索人类造血和产生各种功能血细胞的框架。有关本协议使用和执行的完整细节,请参阅Shen等人1和Qu等人2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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