利用细胞术技术研究干细胞生物学

H. Nakauchi
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引用次数: 0

摘要

造血干细胞(Hematopoietic stem cells, hsc)是目前研究最多的干细胞,为干细胞生物学的发展做出了巨大贡献。造血干细胞以非分裂状态存在于骨髓壁龛中,偶尔会被唤醒进行细胞分裂。通过流式细胞术使用高度纯化的造血干细胞,我们最近发现细胞因子处理造血干细胞导致脂筏标记物GM1神经节苷脂的极化以及Akt的磷酸化和FOXO3a向细胞质的转移。细胞因子诱导的脂筏聚集是HSC重新进入细胞周期的必要条件。此外,基于来自生态位信号抑制LRC并诱导hsc冬眠的假设,我们筛选了抑制LRC的候选生态位信号。在检测的生态位信号中,转化生长因子-β (TGF-β)有效抑制LRC并诱导p57Kip2表达,导致HSC在体外冬眠。这些数据确立了TGF-β作为一个生态位信号在控制HSC冬眠中的作用,为鉴定骨髓干细胞生态位提供了重要线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of cytometry technology for the study of stem cell biology
Hematopoietic stem cells (HSCs) are best-studied stem cells and they have contributed a great deal for the development of stem cell biology. HSCs reside in a bone marrow niche in a non-dividing state from which they occasionally are aroused to undergo cell division. Using highly purified HSCs by flow cytometry, we have recently shown that cytokine treatment of HSCs led to polarization of the lipid raft marker GM1 ganglioside as well as to phosphorylation of Akt and relocation of FOXO3a to the cytoplasm. Lipid raft clustering induced by cytokines is essential for HSC re-entry into the cell cycle. Furthermore, based on a hypothesis that signals from the niche inhibit LRC and induce hibernation in HSCs, we screened candidate niche signals for inhibition of LRC. Among niche signals examined, transforming growth factor-β (TGF-β) efficiently inhibits LRC and induces p57Kip2 expression, leading to HSC hibernation ex vivo. These data establish the role of TGF-β as a niche signal in control of HSC hibernation and provide important clues to identify stem cell niche in bone marrow.
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