TY - JOUR
T1 - Mitochondrial Deep Dive into Hematopoietic Stem Cell Dormancy
T2 - Not Much Glycolysis but Plenty of Sluggish Lysosomes
AU - Qiu, Jiajing
AU - Ghaffari, Saghi
N1 - Funding Information:
This work was supported by National Heart, Lung, and Blood Institute Grants R01HL161567, R01HL136255, R01CA205975 and New York State Stem Cell Science Investigator Initiated Research Project (NYSTEM IIRP) Award C32602GG to SG.
Publisher Copyright:
© 2022 ISEH – Society for Hematology and Stem Cells
PY - 2022/10
Y1 - 2022/10
N2 - The discovery of hematopoietic stem cells (HSCs) heterogeneity has had major implications for investigations of hematopoietic stem cell disorders, clonal hematopoiesis, and HSC aging. More recent studies of the heterogeneity of HSCs' organelles have begun to provide additional insights into HSCs' behavior with far-reaching ramifications for the mechanistic understanding of aging of HSCs and stem cell-derived diseases. Mitochondrial heterogeneity has been explored to expose HSC subsets with distinct properties and functions. Here we review some of the recent advances in these lines of studies that challenged the classic view of glycolysis in HSCs and led to the identification of lysosomes as dynamic pivotal switches in controlling HSC quiescence versus activation beyond their function in autophagy.
AB - The discovery of hematopoietic stem cells (HSCs) heterogeneity has had major implications for investigations of hematopoietic stem cell disorders, clonal hematopoiesis, and HSC aging. More recent studies of the heterogeneity of HSCs' organelles have begun to provide additional insights into HSCs' behavior with far-reaching ramifications for the mechanistic understanding of aging of HSCs and stem cell-derived diseases. Mitochondrial heterogeneity has been explored to expose HSC subsets with distinct properties and functions. Here we review some of the recent advances in these lines of studies that challenged the classic view of glycolysis in HSCs and led to the identification of lysosomes as dynamic pivotal switches in controlling HSC quiescence versus activation beyond their function in autophagy.
UR - http://www.scopus.com/inward/record.url?scp=85136256747&partnerID=8YFLogxK
U2 - 10.1016/j.exphem.2022.07.299
DO - 10.1016/j.exphem.2022.07.299
M3 - Review article
C2 - 35908627
AN - SCOPUS:85136256747
VL - 114
SP - 1
EP - 8
JO - Experimental Hematology
JF - Experimental Hematology
SN - 0301-472X
ER -