p63 regulates the caspase-8-FLIP apoptotic pathway in epidermis

被引:33
作者
Borrelli, S. [1 ]
Candi, E. [2 ]
Alotto, D. [3 ]
Castagnoli, C. [3 ]
Melino, G. [2 ,4 ]
Vigano, M. A. [1 ]
Mantovani, R. [1 ]
机构
[1] Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
[2] Univ Roma Tor Vergata, Biochem IDI IRCCS Lab, I-00133 Rome, Italy
[3] Osped CTO, Dipartimento Chirurg Plast, Turin, Italy
[4] Univ Leicester, Toxicol Unit, MRC, Leicester LE1 9HN, Leics, England
基金
英国医学研究理事会;
关键词
p63; keratinocytes; caspase; 8; FLIP; apoptosis; RECEPTOR-INDUCED APOPTOSIS; B-INDUCED APOPTOSIS; SIGNALING COMPLEX; HUMAN KERATINOCYTES; P53; HOMOLOG; C-FLIPR; ACTIVATION; CELLS; PROLIFERATION; PROTEIN;
D O I
10.1038/cdd.2008.147
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 transcription factor p63, member of the p53 family, is crucial for epithelial development. An RNAi screening identified the apoptotic gene Procaspase-8 as a target activated by p63. The caspase-8 inhibitor FLIP is also under p63 control. We analysed and detailed the direct transactivation through the use of RNAi, reporter assays, ChIPs, western blots, confocal studies in HaCat, as well as in primary human keratinocytes. The direct Delta Np63 regulation of these targets was confirmed in vivo using transgenic Delta Np63 mice under the K5 promoter, as compared with p63 knockout mice, and in vitro in normal human primary keratinocytes following UV irradiation. Lowering the steady state of p63 protein levels changes the relative ratio of FLIP isoforms, causing the activation of the expressed, inactive Procaspase-8, into the active isoform thus triggering the proapoptotic cascade. Therefore, p63 fine-tunes the Procaspase-8-FLIP pro- and antiapoptotic pathway in keratinocytes.
引用
收藏
页码:253 / 263
页数:11
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