TGF-β信号传导及其在造血干细胞调控中的作用。

Systems and Synthetic Biology Pub Date : 2015-06-01 Epub Date: 2015-01-29 DOI:10.1007/s11693-015-9161-2
Anuradha Vaidya, Vaijayanti P Kale
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引用次数: 57

摘要

转化生长因子-β (TGF-βs)及其包括骨形态发生蛋白和激活素在内的家族成员参与了造血干细胞(hsc)的增殖、休眠、静止和分化的调控。越来越多的证据表明,TGF-βs超家族在干细胞与其微环境之间以及细胞内的细胞间串扰中发挥着不可或缺的作用。已知造血活性部位,如胎儿肝脏和骨髓中存在丰富的TGF-β,表明其在造血维持和调节中的重要性。TGF-β超家族的一个显著特征是它们所引起的各种效应,取决于应答细胞的发育历史。在本综述中,我们讨论了smad依赖性和smad非依赖性TGF-β信号通路,以了解和强调它们在hsc调控中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TGF-β signaling and its role in the regulation of hematopoietic stem cells.

Transforming growth factor-betas (TGF-βs) and their family members that include bone morphogenic proteins and activins have been implicated in the regulation of proliferation, hibernation, quiescence and differentiation of hematopoietic stem cells (HSCs). Increasing evidence suggests that the superfamily of TGF-βs play an integral role in the intercellular cross-talk between the stem cells and their microenvironment as well as within the cells at an intracellular level. Active sites of hematopoiesis, such as fetal liver and bone marrow are known to have abundant presence of TGF-β indicating their importance in the maintenance and regulation of hematopoiesis. One of the striking features of TGF-β superfamily is the variety of effects they evoke, contingent on the developing history of the responding cells. In the present review, we discuss the Smad-dependent and Smad-independent TGF-β signaling pathways in order to understand and underscore their role in the regulation of HSCs.

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