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弓形虫在体外对细胞色素c诱导的半胱天冬酶激活的直接抑制揭示了干扰宿主细胞凋亡的新机制。

Direct inhibition of cytochrome c-induced caspase activation in vitro by Toxoplasma gondii reveals novel mechanisms of interference with host cell apoptosis.

作者信息

Keller Philine, Schaumburg Frieder, Fischer Silke F, Häcker Georg, Gross Uwe, Lüder Carsten G K

机构信息

Institut für Medizinische Mikrobiologie, Georg-August-Universität, Göttingen, Germany.

出版信息

FEMS Microbiol Lett. 2006 May;258(2):312-9. doi: 10.1111/j.1574-6968.2006.00241.x.

Abstract

The intracellular parasite Toxoplasma gondii is known to inhibit apoptosis of its host cell. The molecular mechanisms of this interference are, however, not yet completely understood. We show here that viable parasites prominently inhibited the activation of caspase 3/7 induced by cytochrome c, dATP and dithiothreitol in cytosolic extracts of human-derived Jurkat leukemic T cells. In contrast, granzyme B-induced caspase activity was only slightly diminished. De novo protein biosynthesis by T. gondii was dispensable for the inhibition of cytochrome c-induced caspase activation. Furthermore, a complete parasite lysate or, more importantly, molecules released by extracellular parasites mediated the interaction with the caspase cascade. The cell-free system applied here is thus a valuable tool to study the interaction of T. gondii and possibly other intracellular pathogens with host cell apoptosis.

摘要

细胞内寄生虫刚地弓形虫已知可抑制其宿主细胞的凋亡。然而,这种干扰的分子机制尚未完全明确。我们在此表明,活的寄生虫显著抑制了人源Jurkat白血病T细胞胞质提取物中由细胞色素c、dATP和二硫苏糖醇诱导的半胱天冬酶3/7的激活。相比之下,颗粒酶B诱导的半胱天冬酶活性仅略有降低。刚地弓形虫从头合成蛋白质对于抑制细胞色素c诱导的半胱天冬酶激活并非必需。此外,完整的寄生虫裂解物,或者更重要的是,细胞外寄生虫释放的分子介导了与半胱天冬酶级联反应的相互作用。因此,这里应用的无细胞系统是研究刚地弓形虫以及可能的其他细胞内病原体与宿主细胞凋亡相互作用的宝贵工具。

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