Modulation of p53 by mitogen-activated protein kinase pathways and protein kinase C δ during avian reovirus S1133-induced apoptosis

被引:42
作者
Lin, Ping-Yuan [4 ,5 ]
Lee, Jeng-Woei [4 ,5 ]
Liao, Ming-Huei [1 ,2 ,3 ]
Hsu, Hsue-Yin [4 ,5 ]
Chiu, Shu-Jun [4 ,5 ]
Liu, Hung-Jen [1 ,2 ,3 ]
Shih, Wen-Ling [1 ]
机构
[1] Natl Pingtung Univ Sci & Technol, Grad Inst Biotechnol, Neipu 91201, Pingtung, Taiwan
[2] Natl Pingtung Univ Sci & Technol, Grad Inst, Pingtung, Taiwan
[3] Natl Pingtung Univ Sci & Technol, Dept Vet Med, Pingtung, Taiwan
[4] Tzu Chi Univ, Grad Inst, Hualien, Taiwan
[5] Tzu Chi Univ, Dept Life Sci, Hualien, Taiwan
关键词
ARV S1133; p53; PKC delta; MAPK; Apoptosis; TUMOR-SUPPRESSOR P53; VIRUS-INDUCED APOPTOSIS; INDUCED CELL-DEATH; HEPATITIS-B-VIRUS; NF-KAPPA-B; SIGNAL-TRANSDUCTION; TYROSINE PHOSPHORYLATION; MAP KINASES; PKC-DELTA; GENE-EXPRESSION;
D O I
10.1016/j.virol.2008.12.028
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
ARV S1133 infection caused apoptosis in vivo and in vitro: however, the intracellular signaling pathways have not been fully delineated. We have previously demonstrated that ARV S1133 activates proapoptotic signaling from Src to p53, and further investigated how ARV S1133 modulates p53. We found that ARV S1133 forms syncytia and induces apoptosis in CEF, DF1 and Veto cells with different kinetics. Enhancement of p53 phosphorylation and DNA-binding capacity to bax and bad promoters was found in this study to increase bax and bad expression in ARV S1133-infected cells. ARV S1133 activates PKC delta and p38 and JNK/SAPK pathways, and inhibition of Ras, p38, JNK/SAPK and PKC 8 works efficiently against apoptosis. Suppression of p38, JNK/SAPK and PKC 8 selectively abolished ARV S1133-mediated p53 phosphorylation; moreover, inhibition of Src did not affect ARV S1133-induced p38 and JNK/SAPK activation, whereas blocking of Ras resulted in a reduction in the activities of p38 and JNK/SAPK. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 334
页数:12
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