Mitochondria in the maintenance of hematopoietic stem cells: new perspectives and opportunities

被引:124
作者
Filippi, Marie-Dominique [1 ]
Ghaffari, Saghi [2 ,3 ,4 ,5 ]
机构
[1] Cincinnati Childrens Hosp, Div Expt Hematol & Canc Biol, Cincinnati, OH 45229 USA
[2] Icahn Sch Med Mt Sinai, Dept Cell Dev & Regenerat Biol, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, Dev & Stem Cell Biol Multidisciplinary Training, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Black Family Stem Cell Inst, New York, NY USA
[5] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
MARROW STROMAL CELLS; MITOFUSIN; 2; ENDOPLASMIC-RETICULUM; OXIDATIVE-PHOSPHORYLATION; REGULATES QUIESCENCE; PROGENITOR CELLS; PATHWAY; METABOLISM; ACTIVATION; MAINTAINS;
D O I
10.1182/blood-2018-10-808873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The hematopoietic system produces new blood cells throughout life. Mature blood cells all derived from a pool of rare long-lived hematopoietic stem cells (HSCs) that are mostly quiescent but occasionally divide and self-renew to maintain the stem cell pool and to insure the continuous replenishment of blood cells. Mitochondria have recently emerged as critical not only for HSC differentiation and commitment but also for HSC homeostasis. Mitochondria are dynamic organelles that orchestrate a number of fundamental metabolic and signaling processes, producing most of the cellular energy via oxidative phosphorylation. HSCs have a relatively high amount of mitochondria that are mostly inactive. Here, we review recent advances in our understanding of the role of mitochondria in HSC homeostasis and discuss, among other topics, how mitochondrial dynamism and quality control might be implicated in HSC fate, self-renewal, and regenerative potential.
引用
收藏
页码:1943 / 1952
页数:10
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