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DOI 10.1074/jbc.m111.319566

Медицинская библиотека · The Journal of biological chemistry · 2012

Sublytic C5b-9 complexes induce apoptosis of glomerular mesangial cells in rats with Thy-1 nephritis through role of interferon regulatory factor-1-dependent caspase 8 activation.

Liu Lisha, Qiu Wen, Wang Hui, Li Yan, Zhou Jianbo, Xia Mei, Shan Kai, Pang Rongrong, Zhou Ying, Zhao Dan, Wang Yingwei

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The apoptosis of glomerular mesangial cells (GMC) in rat Thy-1 nephritis (Thy-1N), a model of human mesangioproliferative glomerulonephritis, is accompanied by sublytic C5b-9 deposition, but the mechanism of sublytic C5b-9-mediated GMC apoptosis has not been elucidated. In the present study, the gene expression profiles both in the GMC stimulated by sublytic C5b-9 and the rat renal tissue of Thy-1N were detected using microarrays. Among the co-up-regulated genes, the up-regulation of interferon regulatory factor-1 (IRF-1) was further confirmed. Increased caspase 8 and caspase 3 expression and caspase 8 promoter activity in the GMC were also identified. Meanwhile, overexpression or knockdown of IRF-1 not only enhanced or inhibited GMC apoptosis and caspase 8 and 3 induction but also increased or decreased caspase 8 promoter activity, respectively. The element of IRF-1 binding to the caspase 8 promoter was first revealed. Furthermore, silencing IRF-1 or repressing the activation of caspases 8 and 3 significantly reduced GMC apoptosis, including other pathologic changes of Thy-1N. These novel findings indicate that GMC apoptosis of Thy-1N is associated with the IRF-1-activated caspase 8 pathway.

Для цитирования: Liu Lisha, Qiu Wen, Wang Hui, Li Yan, Zhou Jianbo, Xia Mei, Shan Kai, Pang Rongrong, Zhou Ying, Zhao Dan, Wang Yingwei. Sublytic C5b-9 complexes induce apoptosis of glomerular mesangial cells in rats with Thy-1 nephritis through role of interferon regulatory factor-1-dependent caspase 8 activation.. The Journal of biological chemistry. 2012. DOI: 10.1074/jbc.m111.319566.

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