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Use of Cytometry Technology for the Study of Stem Cell Biology

机译:使用细胞术技术对干细胞生物学研究

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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 FOX03a 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 p57~(Kip2) expression, leading to HSC hibernation ex vivo. These data establish the role of TGF-P as a niche signal in control of HSC hibernation and provide important clues to identify stem cell niche in bone marrow.
机译:造血干细胞(HSCs)是最佳研究的干细胞,它们为干细胞生物学的发展贡献了很大的贡献。 HSC在非分割状态下居住在骨髓利基中,从中偶尔会被唤起接受细胞分裂。通过流式细胞术使用高度纯化的HSC,我们最近显示了HSC的细胞因子处理导致脂质筏标志物GM1神经节苷脂的偏振,以及AKT的磷酸化和Fox03a至细胞质的迁移。细胞因子诱导的脂质筏聚合物对于HSC重新进入细胞周期至关重要。此外,基于来自Niche抑制LRC的信号并在HSC中诱导冬眠的假设,我们筛选候选Niche信号进行抑制LRC。在检查的NichE信号中,转化生长因子-β(TGF-β)有效地抑制LRC并诱导P57〜(KIP2)表达,导致HSC冬眠离体。这些数据建立了TGF-P作为核心信号控制HSC冬眠的作用,并提供重要的线索以鉴定骨髓中的干细胞Niche。

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