Skaletskaya A, Bartle L M, Chittenden T, McCormick A L, Mocarski E S, Goldmacher V S
ImmunoGen, 128 Sidney Street, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7829-34. doi: 10.1073/pnas.141108798. Epub 2001 Jun 26.
We have identified a human cytomegalovirus cell-death suppressor, denoted vICA, encoded by the viral UL36 gene. vICA inhibits Fas-mediated apoptosis by binding to the pro-domain of caspase-8 and preventing its activation. vICA does not share significant sequence homology with FLIPs or other known suppressors of apoptosis, suggesting that this protein represents a new class of cell-death suppressors. Notably, resistance to Fas-mediated apoptosis is delayed in fibroblasts infected with viruses that encode mutant vICA, suggesting that vICA suppresses death-receptor-induced cell death in the context of viral infection. Although vICA is dispensable for viral replication in vitro, the common targeting of caspase-8 activation by diverse herpesviruses argues for an important role for this antiapoptotic mechanism in the pathogenesis of viral infection in the host, most likely in avoiding immune clearance by cytotoxic lymphocytes and natural killer cells.
我们已经鉴定出一种由病毒UL36基因编码的人类巨细胞病毒细胞死亡抑制因子,命名为vICA。vICA通过与半胱天冬酶-8的前结构域结合并阻止其激活来抑制Fas介导的细胞凋亡。vICA与FLIPs或其他已知的凋亡抑制因子没有显著的序列同源性,这表明这种蛋白质代表了一类新的细胞死亡抑制因子。值得注意的是,感染编码突变vICA病毒的成纤维细胞对Fas介导的细胞凋亡的抗性会延迟,这表明vICA在病毒感染的情况下抑制死亡受体诱导的细胞死亡。虽然vICA在体外病毒复制中并非必需,但多种疱疹病毒对半胱天冬酶-8激活的共同靶向作用表明,这种抗凋亡机制在宿主病毒感染的发病机制中起着重要作用,很可能是为了避免被细胞毒性淋巴细胞和自然杀伤细胞进行免疫清除。