Hematopoietic Stem Cells Count and Remember Self-Renewal Divisions

被引:201
作者
Bernitz, Jeffrey M. [1 ,2 ,3 ]
Kim, Huen Suk [1 ,2 ,3 ]
MacArthur, Ben [4 ,5 ,6 ]
Sieburg, Hans [7 ]
Moore, Kateri [1 ,2 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Cell Dev & Regenerat Biol, One Gustave L Levy Pl,Box 1496, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Black Family Stem Cell Inst, One Gustave L Levy Pl,Box 1496, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, One Gustave L Levy Pl,Box 1496, New York, NY 10029 USA
[4] Univ Southampton, Math Sci, Southampton SO17 1BJ, Hants, England
[5] Univ Southampton, Ctr Human Dev Stem Cells & Regenerat, Fac Med, Southampton SO17 1BJ, Hants, England
[6] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[7] Vaccine Res Inst San Diego, San Diego, CA 92121 USA
关键词
NEURONAL ISOFORM; DORMANCY; DRIVEN; CPEB;
D O I
10.1016/j.cell.2016.10.022
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 ability of cells to count and remember their divisions could underlie many alterations that occur during development, aging, and disease. We tracked the cumulative divisional history of slow-cycling hematopoietic stem cells (HSCs) throughout adult life. This revealed a fraction of rarely dividing HSCs that contained all the long-term HSC (LT- HSC) activity within the aging HSC compartment. During adult life, this population asynchronously completes four traceable symmetric self-renewal divisions to expand its size before entering a state of dormancy. We show that the mechanism of expansion involves progressively lengthening periods between cell divisions, with long-term regenerative potential lost upon a fifth division. Our data also show that age-related phenotypic changes within the HSC compartment are divisional history dependent. These results suggest that HSCs accumulate discrete memory stages over their divisional history and provide evidence for the role of cellular memory in HSC aging.
引用
收藏
页码:1296 / +
页数:24
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