TNF/TNF受体和Fas配体对小鼠内毒素血症和细菌性腹膜炎模型毒性的贡献。

Journal of inflammation Pub Date : 1995-01-01
D Heumann, D Le Roy, G Zanetti, H P Eugster, B Ryffel, M Hahne, J Tschopp, M P Glauser
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引用次数: 0

摘要

Fas/Fas配体和TNF/TNF受体参与细胞凋亡。到目前为止,这两个系统是否与感染性休克有关还没有确定。我们研究了TNF/TNFR和Fas/Fas配体在小鼠内毒素血症和特异性血症模型中的作用。在LPS刺激下,TNF和TNFR p55参与了诱导死亡的过程。FasL不增加致死性,在金鼠实验中证实了这一点。在腹腔注射活大肠杆菌后,TNF和TNFR p55是对抗感染所必需的。任何一种基因的破坏都与增强的致死率和无法清除细菌有关。在该腹膜炎模型中,对金鼠无影响。因此,这些观察结果证实了TNF/TNFR在内毒素血症中的致病作用及其在局部细菌感染中的有益作用。此外,这些数据排除了Fas/FasL在小鼠感染性休克中的主要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contribution of TNF/TNF receptor and of Fas ligand to toxicity in murine models of endotoxemia and bacterial peritonitis.

Fas/Fas ligand and TNF/TNF receptors are involved in apoptosis. Whether both systems are involved in septic shock has not been determined so far. We investigated the role of TNF/TNFR and Fas/Fas ligand in models of endotoxemia and of speticemia in mice. Upon LPS challenge, TNF and TNFR p55 were involved in the process inducing lethality. FasL did not contribute to enhance lethality, as evidenced in gld mice, lacing FasL. Following an intraperitoneal injection of live E. coli, TNF and TNFR p55 were necessary to combat infection. Disruption of either gene was associated with enhanced lethality and failure to clear the bacteria. No effect observed in gld mice in this peritonitis model. Thus, these observations confirmed the pathogenic role of TNF/TNFR in endotoxemia and its beneficial role in local bacterial infections. In addition the data ruled out a major role for Fas/FasL in septic shock in mice.

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