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骨形态发生蛋白(BMP)和白细胞介素-3(IL-3)信号通路在小鼠胚胎造血干细胞调控中的作用。

The roles of BMP and IL-3 signaling pathways in the control of hematopoietic stem cells in the mouse embryo.

作者信息

Robin Catherine, Durand Charles

机构信息

Department of Cell Biology and Erasmus Stem Cell Institute, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Int J Dev Biol. 2010;54(6-7):1189-200. doi: 10.1387/ijdb.093040cr.

Abstract

During mouse ontogeny, the first adult-type hematopoietic stem cells (HSC) are autonomously generated at mid-gestation in the AGM (Aorta-Gonad-Mesonephros) region. Successively present in different anatomical sites where they will expand, HSCs will finally colonize the bone marrow (BM) where they will reside during the entire adult life. In the bone marrow, both HSC self-renewal and differentiation are controlled at cellular and molecular levels by interactions with the stromal microenvironment. So far, very little is known about the extracellular factors involved in the regulation of embryonic HSC emergence, survival and expansion. In the present review, we outline the BMP and IL-3 signaling pathways that are critical for the growth and potential of embryonic HSCs. We will also discuss how these pathways might be integrated with the ones of Notch and Mpl/thrombopoietin, also identified as important key regulators of AGM HSC activity.

摘要

在小鼠个体发育过程中,第一批成年型造血干细胞(HSC)在妊娠中期于主动脉-性腺-中肾(AGM)区域自主产生。造血干细胞相继出现在不同的解剖部位并在那里增殖,最终定居于骨髓(BM),并在整个成年期都驻留在骨髓中。在骨髓中,造血干细胞的自我更新和分化在细胞和分子水平上受到与基质微环境相互作用的调控。到目前为止,对于参与调节胚胎造血干细胞出现、存活和增殖的细胞外因子了解甚少。在本综述中,我们概述了对胚胎造血干细胞的生长和潜能至关重要的骨形态发生蛋白(BMP)和白细胞介素-3(IL-3)信号通路。我们还将讨论这些信号通路如何与Notch和Mpl/血小板生成素的信号通路整合,后两者也被确定为AGM区造血干细胞活性的重要关键调节因子。

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