Truong Amy B, Kretz Markus, Ridky Todd W, Kimmel Robin, Khavari Paul A
VA Palo Alto Health Care System, Palo Alto, California 94304, USA.
Genes Dev. 2006 Nov 15;20(22):3185-97. doi: 10.1101/gad.1463206.
p63 is a multi-isoform p53 family member required for epidermal development. Contrasting roles for p63 in either the initial commitment to the stratified epithelial cell fate or in stem cell-based self-renewal have been proposed. To investigate p63 function in a post-developmental context, we used siRNAs directed against p63 to down-regulate p63 expression in regenerating human epidermis. Loss of p63 resulted in severe tissue hypoplasia and inhibited both stratification and differentiation in a cell-autonomous manner. Although p63-deficient cells exhibited hypoproliferation, differentiation defects were not due to tissue hypoplasia. Simultaneous p63 and p53 knockdown rescued the cell proliferation defect of p63 knockdown alone but failed to restore differentiation, suggesting that defects in epidermal proliferation and differentiation are mediated via p53-dependent and -independent mechanisms, respectively. Furthermore, DeltaNp63 isoforms are the main mediators of p63 effects, although TAp63 isoforms may contribute to late differentiation. These data indicate that p63 is required for both the proliferative and differentiation potential of developmentally mature keratinocytes.
p63是表皮发育所必需的一种多异构体p53家族成员。关于p63在分层上皮细胞命运的初始决定或基于干细胞的自我更新中所起的作用,已有不同观点。为了研究p63在发育后环境中的功能,我们使用针对p63的小干扰RNA(siRNA)来下调再生人表皮中p63的表达。p63缺失导致严重的组织发育不全,并以细胞自主方式抑制分层和分化。虽然p63缺陷细胞表现出增殖不足,但分化缺陷并非由组织发育不全引起。同时敲低p63和p53可挽救单独敲低p63时的细胞增殖缺陷,但无法恢复分化,这表明表皮增殖和分化缺陷分别通过p53依赖和非依赖机制介导。此外,DeltaNp63异构体是p63作用的主要介导因子,尽管TAp63异构体可能有助于后期分化。这些数据表明,p63对于发育成熟的角质形成细胞的增殖和分化潜能都是必需的。