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弓形虫通过与线粒体依赖性程序性细胞死亡途径的多种相互作用抑制紫外线诱导的细胞凋亡。

Toxoplasma gondii inhibits ultraviolet light-induced apoptosis through multiple interactions with the mitochondrion-dependent programmed cell death pathway.

作者信息

Carmen John C, Hardi Lucia, Sinai Anthony P

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky College of Medicine, Lexington, KY 40536, USA.

出版信息

Cell Microbiol. 2006 Feb;8(2):301-15. doi: 10.1111/j.1462-5822.2005.00622.x.

Abstract

Cells infected with the protozoan parasite Toxoplasma gondii are resistant to diverse apoptotic stimuli. In this study, we perform a detailed analysis of the manipulation of the mitochondrial arm of the apoptotic cascade by the parasite. Apoptosis was induced using irradiation with ultraviolet light (UV), and the kinetics of caspase activation, cytochrome c release and activation of the upstream signalling pathways were examined. The evidence clearly points to T. gondii targeting multiple steps in the transmission [inhibition of c-Jun N-terminal kinase (JNK) activation in response to UV], triggering (inhibition of cytochrome c release by affecting the balance of pro- and anti-apoptotic BCL-2 family members) and execution (inhibition of caspase 9 and caspase 3) phases of the apoptotic cascade. Interestingly, the multilevel pattern of inhibition that emerges suggests that the global inhibition of the mitochondrial arm of apoptosis is not likely to be contributed to by the small subset of mitochondria recruited to the T. gondii parasitophorous vacuole membrane.

摘要

感染原生动物寄生虫刚地弓形虫的细胞对多种凋亡刺激具有抗性。在本研究中,我们对该寄生虫对凋亡级联反应中线粒体途径的操控进行了详细分析。使用紫外线(UV)照射诱导细胞凋亡,并检测了半胱天冬酶激活的动力学、细胞色素c释放以及上游信号通路的激活情况。证据明确表明,刚地弓形虫靶向凋亡级联反应的多个步骤,包括传递阶段(抑制紫外线诱导的c-Jun氨基末端激酶(JNK)激活)、触发阶段(通过影响促凋亡和抗凋亡BCL-2家族成员的平衡来抑制细胞色素c释放)和执行阶段(抑制半胱天冬酶9和半胱天冬酶3)。有趣的是,所呈现的多级抑制模式表明,对凋亡线粒体途径的整体抑制不太可能是由募集到刚地弓形虫寄生泡膜上的一小部分线粒体造成的。

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