重编程
诱导多能干细胞
胚胎干细胞
细胞生物学
生物
干细胞
祖细胞
骨形态发生蛋白
转化生长因子
体细胞
细胞命运测定
细胞分化
细胞
遗传学
转录因子
基因
作者
Wenlin Li,Wanguo Wei,Sheng Ding
出处
期刊:Methods in molecular biology
日期:2016-01-01
卷期号:: 137-145
被引量:11
标识
DOI:10.1007/978-1-4939-2966-5_8
摘要
The transforming growth factor-β (TGF-β) family of cytokines, including TGF-β, bone morphogenic proteins (BMPs), and activin/nodal, is a group of crucial morphogens in embryonic development, and plays key roles in modulating stem/progenitor cell fate. TGF-β signaling is essential in maintaining the pluripotency of human pluripotent stem cells (hPSCs), including both human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs), and its modulation can direct lineage-specific differentiation. Recent studies also demonstrate TGF-β signaling negatively regulates reprogramming and inhibition of TGF-β signaling can enhance reprogramming through facilitating mesenchymal-to-epithelial transition (MET). This chapter introduces methods of modulating somatic cell reprogramming to iPSCs and neural induction from hPSCs through modulating TGF-β signaling by chemical approaches.
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