Jiang Xia, Kanda Tatsuo, Haga Yuki, Sasaki Reina, Nakamura Masato, Wu Shuang, Nakamoto Shingo, Shirasawa Hiroshi, Okamoto Hiroaki, Yokosuka Osamu
Department of Gastroenterology and Nephrology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Department of Molecular Virology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Exp Ther Med. 2017 Jun;13(6):3305-3308. doi: 10.3892/etm.2017.4407. Epub 2017 Apr 28.
Infection with hepatitis A virus (HAV) is a major cause of acute hepatitis globally and it is important to identify the mechanisms of HAV replication. Glucose-regulated protein 78 (GRP78) is an endoplasmic reticulum (ER) chaperone and serves a role in unfolded protein response pathways. Previous studies have demonstrated that GRP78 functions as an endogenous antiviral factor. In the present study, two loss-of-function studies using GRP78 were completed to elucidate the role of GRP78 in HAV infection. HAV replication was observed to be enhanced by deficient GRP78 although GRP78-deficiency also led to lower expression of ER stress molecules downstream of GRP78. Therefore, GRP78 appears to be a potential novel defensive molecule against HAV in hepatocytes.
甲型肝炎病毒(HAV)感染是全球急性肝炎的主要病因,因此确定HAV复制机制很重要。葡萄糖调节蛋白78(GRP78)是一种内质网(ER)伴侣蛋白,在未折叠蛋白反应途径中发挥作用。先前的研究表明,GRP78作为一种内源性抗病毒因子发挥作用。在本研究中,完成了两项使用GRP78的功能丧失研究,以阐明GRP78在HAV感染中的作用。尽管GRP78缺陷也导致GRP78下游内质网应激分子的表达降低,但观察到GRP78缺陷会增强HAV复制。因此,GRP78似乎是肝细胞中一种潜在的新型抗HAV防御分子。