Signalling pathways that control vertebrate haematopoietic stem cell specification

被引:121
作者
Clements, Wilson K. [1 ]
Traver, David [2 ,3 ]
机构
[1] St Jude Childrens Res Hosp, Dept Hematol, Div Expt Hematol, Memphis, TN 38105 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
SMOOTH-MUSCLE-CELLS; BONE MORPHOGENETIC PROTEIN-4; RECEPTOR-LIKE RECEPTOR; BETA-CATENIN; DEFINITIVE HEMATOPOIESIS; LONG-TERM; YOLK-SAC; ARTERIAL DIFFERENTIATION; AORTIC ENDOTHELIUM; NERVOUS-SYSTEM;
D O I
10.1038/nri3443
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Haematopoietic stem cells (HSCs) are tissue-specific stem cells that replenish all mature blood lineages during the lifetime of an individual. Clinically, HSCs form the foundation of transplantation-based therapies for leukaemias and congenital blood disorders. Researchers have long been interested in understanding the normal signalling mechanisms that specify HSCs in the embryo, in part because recapitulating these requirements in vitro might provide a means to generate immune-compatible HSCs for transplantation. Recent embryological work has demonstrated the existence of previously unknown signalling requirements. Moreover, it is now clear that gene expression in the nearby somite is integrally involved in regulating the transition of the embryonic endothelium to a haemogenic fate. Here, we review current knowledge of the intraembryonic signals required for the specification of HSCs in vertebrates.
引用
收藏
页码:336 / 348
页数:13
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