| Literature DB >> 27426727 |
Jie Zan1, Juan Liu1, Jian-Wei Zhou1, Hai-Long Wang1, Kai-Kun Mo1, Yan Yan1, Yun-Bin Xu1, Min Liao1, Shuo Su2, Rong-Liang Hu3, Ji-Yong Zhou4.
Abstract
Apoptosis, as an innate antiviral defense, not only functions to limit viral replication by eliminating infected cells, but also contribute to viral dissemination, particularly at the late stages of infection. A highly neurotropic CVS strain of rabies virus induces apoptosis both in vitro and in vivo. However, the detailed mechanism of CVS-mediated neuronal apoptosis is not entirely clear. Here, we show that CVS induces apoptosis through mitochondrial pathway by dissipating mitochondrial membrane potential, release of cytochrome c and AIF. CVS blocks Bax activation at the early stages of infection; while M protein partially targets mitochondria and induces mitochondrial apoptosis at the late stages of infection. The α-helix structure spanning 67-79 amino acids of M protein is essential for mitochondrial targeting and induction of apoptosis. These results suggest that CVS functions on mitochondria to regulate apoptosis at different stages of infection, so as to for viral replication and dissemination.Entities:
Keywords: Apoptosis; Matrix protein; Mitochondria; Rabies virus
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Year: 2016 PMID: 27426727 DOI: 10.1016/j.yexcr.2016.07.008
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905