TY - JOUR
T1 - Mitochondria in the maintenance of hematopoietic stem cells
T2 - New perspectives and opportunities
AU - Filippi, Marie Dominique
AU - Ghaffari, Saghi
N1 - Funding Information:
The work in the laboratory of M.-D.F. was supported by National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases grant R01 DK102890 and National Institute of General Medical Sciences grant R01GM112792. The work in the laboratory of S.G. was supported by National Institutes of Health, National Heart, Lung, and Blood Institute grant R01HL136255, National Cancer Institute grant R01CA205975, and funds from New York State Stem Cell Science (NYSTEM) Investigator Initiated Research Projects (IIRP) grant C32602GG.
Publisher Copyright:
© 2019 by The American Society of Hematology.
PY - 2019/5/2
Y1 - 2019/5/2
N2 - 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 ho-meostasis. 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.
AB - 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 ho-meostasis. 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.
UR - http://www.scopus.com/inward/record.url?scp=85065563657&partnerID=8YFLogxK
U2 - 10.1182/blood-2018-10-808873
DO - 10.1182/blood-2018-10-808873
M3 - Review article
C2 - 30808633
AN - SCOPUS:85065563657
SN - 0006-4971
VL - 133
SP - 1943
EP - 1952
JO - Blood
JF - Blood
IS - 18
ER -