Hematopoietic stem cell niche maintenance during homeostasis and regeneration

被引:599
|
作者
Mendelson, Avital [1 ,2 ]
Frenette, Paul S. [1 ,2 ,3 ]
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[2] Ruth L & David S Gottesman Inst Stem Cell & Regen, Bronx, NY USA
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
关键词
BONE-MARROW MICROENVIRONMENT; SELF-RENEWAL; PROGENITOR CELLS; BETA-CATENIN; N-CADHERIN; ENDOTHELIAL-CELLS; LONG-TERM; FUNCTIONALLY DISTINCT; RETINOIC ACID; STROMAL CELLS;
D O I
10.1038/nm.3647
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bone marrow niche has mystified scientists for many years, leading to widespread investigation to shed light into its molecular and cellular composition. Considerable efforts have been devoted toward uncovering the regulatory mechanisms of hematopoietic stem cell (HSC) niche maintenance. Recent advances in imaging and genetic manipulation of mouse models have allowed the identification of distinct vascular niches that have been shown to orchestrate the balance between quiescence, proliferation and regeneration of the bone marrow after injury. Here we highlight the recently discovered intrinsic mechanisms, microenvironmental interactions and communication with surrounding cells involved in HSC regulation, during homeostasis and in regeneration after injury and discuss their implications for regenerative therapy.
引用
收藏
页码:833 / 846
页数:14
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