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造血生长因子对体外干细胞的作用。

Effects of hemopoietic growth factors on stem cells in vitro.

作者信息

Ogawa M

机构信息

VA Medical Center, Charleston, South Carolina.

出版信息

Hematol Oncol Clin North Am. 1989 Sep;3(3):453-64.

PMID:2698877
Abstract

The central feature of hemopoiesis is the lifelong, stable cell renewal. This process is supported by hemopoietic stem cells, which in the steady-state appear to be dormant in cell cycling. The entry into cell cycle of the dormant stem cells may be promoted by such factors as IL-1, IL-6, and G-CSF. Available evidence indicates that the effects of IL-1 on stem cells are indirectly mediated in part by IL-6 and G-CSF. Once the stem cells leave G0 and begin proliferation, the subsequent process is characterized by continued proliferation and differentiation. While several models of stem cell differentiation have been proposed, micromanipulation studies of individual progenitors suggest that the commitment of multipotential progenitors to single lineages is a stochastic (random) process. The proliferation of early hemopoietic progenitors appears to be supported by IL-3, IL-4, and/or GM-CSF. Once the progenitors are committed to individual lineages, the subsequent maturation process appears to be supported by late-acting, lineage-specific factors such as Ep (for erythropoiesis), G-CSF (for neutrophil production), and IL-5 (for eosinophilopoiesis). Thus, hemopoietic proliferation appears to be regulated by a cascade of factors directed at different developmental stages.

摘要

造血作用的核心特征是终身性的稳定细胞更新。这一过程由造血干细胞支持,在稳态下,造血干细胞在细胞周期中似乎处于休眠状态。诸如白细胞介素-1(IL-1)、白细胞介素-6(IL-6)和粒细胞集落刺激因子(G-CSF)等因子可促进休眠干细胞进入细胞周期。现有证据表明,IL-1对干细胞的作用部分是通过IL-6和G-CSF间接介导的。一旦干细胞离开G0期并开始增殖,随后的过程以持续增殖和分化为特征。虽然已经提出了几种干细胞分化模型,但对单个祖细胞的显微操作研究表明,多能祖细胞向单一谱系的定向分化是一个随机过程。早期造血祖细胞的增殖似乎由IL-3、IL-4和/或粒细胞-巨噬细胞集落刺激因子(GM-CSF)支持。一旦祖细胞定向分化为单个谱系,随后的成熟过程似乎由后期作用的、谱系特异性因子支持,如促红细胞生成素(Ep,用于红细胞生成)、G-CSF(用于中性粒细胞生成)和IL-5(用于嗜酸性粒细胞生成)。因此,造血增殖似乎受针对不同发育阶段的一系列因子调控。

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