首页> 外文期刊>Applied biochemistry and biotechnology, Part A. enzyme engineering and biotechnology >Canine Parvovirus Type 2a (CPV-2a)-Induced Apoptosis in MDCK Involves Both Extrinsic and Intrinsic Pathways
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Canine Parvovirus Type 2a (CPV-2a)-Induced Apoptosis in MDCK Involves Both Extrinsic and Intrinsic Pathways

机译:犬细小病毒2a型(CPV-2a)诱导的MDCK细胞凋亡涉及外部和内部途径。

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摘要

The canine parvovirus type 2 (CPV-2) causes an acute disease in dogs. It has been found to induce cell cycle arrest and DNA damage leading to cellular lysis. In this paper, we evaluated the apoptotic potential of the "new CPV-2a" in MDCK cells and elucidated the mechanism of the induction of apoptosis. The exposure of MDCK cells to the virus was found to trigger apoptotic response. Apoptosis was confirmed by phosphatidylserine translocation, DNA fragmentation assays, and cell cycle analysis. Activation of caspases-3, -8, -9, and -12 and decrease in mitochondrial potential in CPV-2a-infected MDCK cells suggested that the CPV-2a-induced apoptosis is caspase dependent involving extrinsic, intrinsic, and endoplasmic reticulum pathways. Increase in p53 and Bax/Bcl2 ratio was also observed in CPV-2a-infected cells.
机译:2型犬细小病毒(CPV-2)引起犬的急性疾病。已经发现诱导细胞周期停滞和DNA损伤导致细胞裂解。在本文中,我们评估了“新的CPV-2a”在MDCK细胞中的凋亡潜力,并阐明了诱导凋亡的机制。发现MDCK细胞暴露于病毒可引发凋亡反应。通过磷脂酰丝氨酸易位,DNA片段化测定和细胞周期分析来确认凋亡。 CSPA-2a感染的MDCK细胞中caspases-3,-8,-9和-12的激活以及线粒体电位的降低表明CPV-2a诱导的凋亡是caspase依赖性的,涉及外在,内在和内质网途径。在CPV-2a感染的细胞中也观察到p53和Bax / Bcl2比增加。

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