Hematopoietic stem cell: self-renewal versus differentiation

被引:607
作者
Seita, Jun [1 ]
Weissman, Irving L. [1 ]
机构
[1] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-BETA; COLONY-FORMING CELLS; COMMON LYMPHOID PROGENITORS; RECEPTOR TYROSINE KINASE; W-MUTANT MICE; BONE-MARROW; LONG-TERM; TGF-BETA; C-KIT; TRANSFORMING GROWTH-FACTOR-BETA-1;
D O I
10.1002/wsbm.86
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The mammalian blood system, containing more than 10 distinct mature cell types, stands on one specific cell type, hematopoietic stem cell (HSC). Within the system, only HSCs possess the ability of bothmultipotency and self-renewal. Multipotency is the ability to differentiate into all functional blood cells. Self-renewal is the ability to give rise to HSC itself without differentiation. Since mature blood cells (MBCs) are predominantly short-lived, HSCs continuously provide more differentiated progenitors while properly maintaining the HSC pool size throughout life by precisely balancing self-renewal and differentiation. Thus, understanding the mechanisms of self-renewal and differentiation of HSC has been a central issue. In this review, we focus on the hierarchical structure of the hematopoietic system, the current understanding of microenvironment and molecular cues regulating self-renewal and differentiation of adult HSCs, and the currently emerging systems approaches to understand HSC biology. (C) 2010 John Wiley & Sons, Inc. WIREs Syst Biol Med 2010 2 640-653
引用
收藏
页码:640 / 653
页数:14
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