Ray R B, Meyer K, Steele R, Shrivastava A, Aggarwal B B, Ray R
Division of Infectious Diseases and Immunology, Saint Louis University, Missouri 63110, USA.
J Biol Chem. 1998 Jan 23;273(4):2256-9. doi: 10.1074/jbc.273.4.2256.
Hepatitis C virus (HCV) putative core protein has displayed many intriguing biological properties. Since tumor necrosis factor (TNF) plays an important role in controlling viral infection, in this study the effect of the core protein was investigated on the TNF-alpha induced apoptosis of human breast carcinoma cells (MCF7). HCV core protein when expressed inhibited TNF-alpha-induced apoptotic cell death unlike the control MCF7 cells, as determined by cell viability and DNA fragmentation analysis. Additionally, HCV core protein blocked the TNF-induced proteolytic cleavage of the death substrate poly(ADP-ribose) polymerase from its native 116-kDa protein to the characteristic 85-kDa polypeptide. Results from this study suggest that the HCV core protein plays a role in the inhibition of TNF-alpha-mediated cell death. Thus, the ability of core protein to inhibit the TNF-mediated apoptotic signaling pathway may provide a selective advantage for HCV replication, allowing for evasion of host antiviral defense mechanisms.
丙型肝炎病毒(HCV)推定的核心蛋白已展现出许多引人关注的生物学特性。由于肿瘤坏死因子(TNF)在控制病毒感染中发挥重要作用,因此在本研究中,我们探究了核心蛋白对肿瘤坏死因子-α(TNF-α)诱导的人乳腺癌细胞(MCF7)凋亡的影响。通过细胞活力和DNA片段化分析确定,与对照MCF7细胞不同,HCV核心蛋白表达时可抑制TNF-α诱导的凋亡性细胞死亡。此外,HCV核心蛋白可阻断TNF诱导的死亡底物聚(ADP-核糖)聚合酶从其天然的116 kDa蛋白到特征性的85 kDa多肽的蛋白水解切割。本研究结果表明,HCV核心蛋白在抑制TNF-α介导的细胞死亡中发挥作用。因此,核心蛋白抑制TNF介导的凋亡信号通路的能力可能为HCV复制提供选择性优势,从而逃避宿主抗病毒防御机制。