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解读乙肝病毒受体之谜:历史视角

Deciphering the mystery of hepatitis B virus receptors: A historical perspective.

作者信息

Rehman Zaira, Fahim Ammad, Sadia Hajra

机构信息

Healthcare Biotechnology Department, Atta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences & Technology (NUST), Sector H-12, Islamabad, Pakistan.

出版信息

Virusdisease. 2015 Sep;26(3):97-104. doi: 10.1007/s13337-015-0260-1. Epub 2015 Jul 3.

Abstract

Hepatitis B virus is one of the major reasons of viral hepatitis with an estimated 350 million infected patients worldwide. Although, the virus was discovered and cloned more than three decades ago, its entry mechanism has still been in investigation. Numerous potential candidates have been proposed and investigated rigorously to reveal HBV entry mechanism and to unveil the first door of viral entry to hepatocytes. This review provides a short account of role of receptors for entry of HBV into hepatocytes. The viral preS1 region of large surface protein is involved in the attachment of HBV to hepatocytes. The putative attachment site of HBV is located at amino acids 21-47 of preS1. So far, several proteins have been proposed to interact with these different regions of the preS1 domain which includes human immunoglobulin A receptor, glyceraldehyde-3-phosphate dehydrogenase, interleukin-6, a 31-kDa protein, HBV binding factor, asialoglycoprotein receptor, nascent polypeptide-associated complex α polypeptide, lipoprotein lipase, hepatocyte-associated heparan sulfate proteoglycans, glucose-regulated protein 75. However, none of them have appeared to be generally accepted as a true receptor for the virus until recently when sodium taurocholate cotransporting polypeptide identified as HBV entry receptor. Current review provides scientific historical perspective of various candidates known to be interacting with preS1 of HBV for their possible role in viral entry.

摘要

乙型肝炎病毒是病毒性肝炎的主要病因之一,全球估计有3.5亿感染者。尽管该病毒在三十多年前就已被发现和克隆,但其进入机制仍在研究中。人们提出了许多潜在的候选物并进行了严格研究,以揭示乙肝病毒的进入机制,并揭开病毒进入肝细胞的第一道门。这篇综述简要介绍了乙肝病毒进入肝细胞的受体的作用。大表面蛋白的病毒前S1区参与乙肝病毒与肝细胞的附着。乙肝病毒的假定附着位点位于前S1的21-47位氨基酸处。到目前为止,已经提出了几种蛋白质与前S1结构域的这些不同区域相互作用,其中包括人免疫球蛋白A受体、甘油醛-3-磷酸脱氢酶、白细胞介素-6、一种31 kDa的蛋白质、乙肝病毒结合因子、去唾液酸糖蛋白受体、新生多肽相关复合物α多肽、脂蛋白脂肪酶、肝细胞相关硫酸乙酰肝素蛋白聚糖、葡萄糖调节蛋白75。然而,直到最近牛磺胆酸钠共转运多肽被确定为乙肝病毒进入受体之前,它们中没有一个被普遍认为是该病毒的真正受体。本综述提供了各种已知与乙肝病毒前S1相互作用的候选物在病毒进入中可能作用的科学历史视角。

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