Caspase activation and disruption of mitochondrial membrane potential during UV radiation-induced apoptosis of human keratinocytes requires activation of protein kinase C

被引:168
作者
Denning, MF [1 ]
Wang, Y [1 ]
Tibudan, S [1 ]
Alkan, S [1 ]
Nickoloff, BJ [1 ]
Qin, JZ [1 ]
机构
[1] Loyola Univ, Med Ctr, Dept Pathol, Cardinal Bernardin Canc Ctr,Skin Canc Res Program, Maywood, IL 60153 USA
关键词
keratinocyte; ultraviolet radiation; protein kinase C; caspase; mitochondria;
D O I
10.1038/sj.cdd.4400929
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 induction of apoptosis in human keratinocytes by UV radiation involves caspase-mediated cleavage and activation of protein kinase C delta (PKCdelta). Here we examined the role of PKC activation in caspase activation and disruption of mitochondria function by UV radiation. Inhibition of PKC partially blocked UV radiation-induced cleavage of PKCdelta, pro-caspase-3, and pro-caspase-8, and the activation of these caspases. PKC inhibition also blocked the UV-induced loss of mitochondria membrane potential, but did not block the release of cytochrome c from mitochondria, Expression of the active catalytic domain of PKCdelta was sufficient to induce apoptosis and disrupt mitochondrial membrane potential, however a kinase inactive PKCdelta catalytic domain did not, Furthermore, the PKCdelta catalytic fragment generated following UV radiation localized to the mitochondria fraction, as did ectopically expressed PKCdelta catalytic domain. These results identify a functional role for PKC activation in potentiating caspase activation and disrupting mitochondrial function during UV-induced apoptosis.
引用
收藏
页码:40 / 52
页数:13
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