Su Xiaohua, Paris Maryline, Gi Young Jin, Tsai Kenneth Y, Cho Min Soon, Lin Yu-Li, Biernaskie Jeffrey A, Sinha Satrajit, Prives Carol, Pevny Larysa H, Miller Freda D, Flores Elsa R
Department of Molecular and Cellular Oncology, Graduate School of Biomedical Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Cell Stem Cell. 2009 Jul 2;5(1):64-75. doi: 10.1016/j.stem.2009.04.003.
The cellular mechanisms that regulate the maintenance of adult tissue stem cells are still largely unknown. We show here that the p53 family member, TAp63, is essential for maintenance of epidermal and dermal precursors and that, in its absence, these precursors senesce and skin ages prematurely. Specifically, we have developed a TAp63 conditional knockout mouse and used it to ablate TAp63 in the germline (TAp63(-/-)) or in K14-expressing cells in the basal layer of the epidermis (TAp63(fl/fl);K14cre+). TAp63(-/-) mice age prematurely and develop blisters, skin ulcerations, senescence of hair follicle-associated dermal and epidermal cells, and decreased hair morphogenesis. These phenotypes are likely due to loss of TAp63 in dermal and epidermal precursors since both cell types show defective proliferation, early senescence, and genomic instability. These data indicate that TAp63 serves to maintain adult skin stem cells by regulating cellular senescence and genomic stability, thereby preventing premature tissue aging.
调节成体组织干细胞维持的细胞机制在很大程度上仍然未知。我们在此表明,p53家族成员TAp63对于维持表皮和真皮前体细胞至关重要,并且在其缺失时,这些前体细胞会衰老,皮肤会过早老化。具体而言,我们构建了一种TAp63条件性敲除小鼠,并利用它在种系中(TAp63(-/-))或表皮基底层中表达K14的细胞中(TAp63(fl/fl);K14cre+)敲除TAp63。TAp63(-/-)小鼠过早衰老,并出现水泡、皮肤溃疡、毛囊相关的真皮和表皮细胞衰老以及毛发形态发生减少。这些表型可能是由于真皮和表皮前体细胞中TAp63的缺失,因为这两种细胞类型均表现出增殖缺陷、早期衰老和基因组不稳定。这些数据表明,TAp63通过调节细胞衰老和基因组稳定性来维持成体皮肤干细胞,从而防止组织过早老化。