p53-Mediated Hematopoietic Stem and Progenitor Cell Competition

被引:279
作者
Bondar, Tanya [1 ,2 ]
Medzhitov, Ruslan [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06510 USA
关键词
WILD-TYPE P53; DNA-DAMAGE; RADIATION SENSITIVITY; NICHE OCCUPANCY; B-LYMPHOCYTES; MICE; REPAIR; SELECTION; RADIOSENSITIVITY; COMPARTMENTS;
D O I
10.1016/j.stem.2010.03.002
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Cell competition was originally described in Drosophila as a process for selection of the fittest cells. It is likely to play an important role in tissue homeostasis in all metazoans, but little is known about its role and regulation in mammals. By using genetic mosaic mouse models and bone marrow chimeras, we describe here a form of cell competition that selects for the least damaged cells. This competition is controlled by p53 but is distinct from the classical p53-mediated DNA damage response: it persists for months, is specific to the hematopoietic stem and progenitor cells, and depends on the relative rather than absolute level of p53 in competing cells. The competition appears to be mediated by a non-cell-autonomous induction of growth arrest and senescence-related gene expression in outcompeted cells with higher p53 activity, p53-mediated cell competition of this type could potentially contribute to the clonal expansion of incipient cancer cells.
引用
收藏
页码:309 / 322
页数:14
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