Vaidya Anuradha, Kale Vaijayanti P
Symbiosis School of Biomedical Sciences (SSBS), Symbiosis International University (SIU), Symbiosis Knowledge Village, Lavale, Mulshi, Pune, 412115 Maharashtra India.
National Centre for Cell Science (NCCS), NCCS Complex, Pune University Campus, Ganeshkhind, Pune, 411007 Maharashtra India.
Syst Synth Biol. 2015 Jun;9(1-2):1-10. doi: 10.1007/s11693-015-9161-2. Epub 2015 Jan 29.
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.
转化生长因子-β(TGF-β)及其家族成员,包括骨形态发生蛋白和激活素,已被证实参与造血干细胞(HSC)的增殖、休眠、静止和分化的调控。越来越多的证据表明,TGF-β超家族在干细胞与其微环境之间以及细胞内水平的细胞间相互作用中发挥着不可或缺的作用。已知造血的活跃部位,如胎儿肝脏和骨髓,含有丰富的TGF-β,这表明它们在造血的维持和调控中具有重要意义。TGF-β超家族的一个显著特征是,它们所引发的效应多种多样,这取决于应答细胞的发育历史。在本综述中,我们将讨论Smad依赖和Smad非依赖的TGF-β信号通路,以便理解并强调它们在造血干细胞调控中的作用。