Boulais Philip E, Frenette Paul S
Department of Cell Biology, The Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, and.
Department of Cell Biology, The Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, and Department of Medicine, Albert Einstein College of Medicine, Bronx, NY.
Blood. 2015 Apr 23;125(17):2621-9. doi: 10.1182/blood-2014-09-570192. Epub 2015 Mar 11.
The hematopoietic stem cell (HSC) niche commonly refers to the pairing of hematopoietic and mesenchymal cell populations that regulate HSC self-renewal, differentiation, and proliferation. Anatomic localization of the niche is a dynamic unit from the developmental stage that allows proliferating HSCs to expand before they reach the bone marrow where they adopt a quiescent phenotype that protects their integrity and functions. Recent studies have sought to clarify the complexity behind the HSC niche by assessing the contributions of specific cell populations to HSC maintenance. In particular, perivascular microenvironments in the bone marrow confer distinct vascular niches that regulate HSC quiescence and the supply of lineage-committed progenitors. Here, we review recent data on the cellular constituents and molecular mechanisms involved in the communication between HSCs and putative niches.
造血干细胞(HSC)微环境通常是指调节HSC自我更新、分化和增殖的造血细胞与间充质细胞群体的配对。从发育阶段来看,微环境的解剖定位是一个动态单位,它允许增殖的HSC在进入骨髓之前进行扩增,在骨髓中HSC会呈现静止表型,以保护其完整性和功能。最近的研究试图通过评估特定细胞群体对HSC维持的贡献来阐明HSC微环境背后的复杂性。特别是,骨髓中的血管周围微环境赋予了独特的血管微环境,可调节HSC的静止状态以及定向祖细胞的供应。在这里,我们综述了有关HSC与假定微环境之间通讯所涉及的细胞成分和分子机制的最新数据。