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gp96 对于人类疱疹病毒 6A(HHV-6A)和 HHV-6B 感染都很关键。

gp96 Is Critical for both Human Herpesvirus 6A (HHV-6A) and HHV-6B Infections.

机构信息

Department of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.

Institute of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.

出版信息

J Virol. 2020 Jun 16;94(13). doi: 10.1128/JVI.00311-20.

Abstract

Human herpesviruses 6A and 6B (HHV-6A and HHV-6B, respectively) are two virus species in the betaherpesvirus subfamily that exhibit T cell tropism. CD46 and CD134 are the cellular receptors for HHV-6A and HHV-6B, respectively. Interestingly, the efficiency of HHV-6A/6B entry is different among different types of target cells despite similar receptor expression levels on these cells. Here, we found that the cellular factor gp96 (also known as glucose-regulated protein 94 [GRP94]) is expressed on the cell surface and interacts with viral glycoprotein Q1 (gQ1) during virus entry. gp96 cell surface expression levels are associated with the efficiency of HHV-6A and HHV-6B entry into target cells. Both loss-of-function and gain-of-function experiments indicated that gp96 plays an important role in HHV-6 infection. Our findings provide new insight into the HHV-6 entry process and might suggest novel therapeutic targets for HHV-6 infection. Although new clinical importance has been revealed for human herpesviruses 6A (HHV-6A) and 6B, much is still unknown about the life cycles of these viruses in target cells. We identified a novel cellular factor, gp96, that is critical for both HHV-6A and -6B entry into host cells. As gp96 can function as an adjuvant in vaccine development for both infectious agents and cancers, it can be a potential therapeutic target for infection by these two viruses.

摘要

人类疱疹病毒 6A 和 6B(分别为 HHV-6A 和 HHV-6B)是β疱疹病毒亚科中的两种病毒,具有 T 细胞趋向性。CD46 和 CD134 分别是 HHV-6A 和 HHV-6B 的细胞受体。有趣的是,尽管这些细胞上的受体表达水平相似,但 HHV-6A/6B 进入的效率在不同类型的靶细胞中是不同的。在这里,我们发现细胞因子 gp96(也称为葡萄糖调节蛋白 94[GRP94])在病毒进入时表达在细胞表面并与病毒糖蛋白 Q1(gQ1)相互作用。gp96 细胞表面表达水平与 HHV-6A 和 HHV-6B 进入靶细胞的效率相关。功能丧失和功能获得实验均表明 gp96 在 HHV-6 感染中起重要作用。我们的发现为 HHV-6 进入过程提供了新的见解,并可能为 HHV-6 感染提供新的治疗靶点。尽管人类疱疹病毒 6A(HHV-6A)和 6B 的新临床重要性已经显现,但这些病毒在靶细胞中的生命周期仍知之甚少。我们确定了一种新型细胞因子 gp96,它对 HHV-6A 和 -6B 进入宿主细胞都至关重要。由于 gp96 可作为传染性病原体和癌症疫苗开发的佐剂,因此它可能成为这两种病毒感染的潜在治疗靶点。

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本文引用的文献

2
Role of PDGF receptor-α during human cytomegalovirus entry into fibroblasts.
Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):E9889-E9898. doi: 10.1073/pnas.1806305115. Epub 2018 Oct 1.
3
An Unbiased Screen for Human Cytomegalovirus Identifies Neuropilin-2 as a Central Viral Receptor.
Cell. 2018 Aug 23;174(5):1158-1171.e19. doi: 10.1016/j.cell.2018.06.028. Epub 2018 Jul 26.
4
Cell entry of a host-targeting protein of oomycetes requires gp96.
Nat Commun. 2018 Jun 14;9(1):2347. doi: 10.1038/s41467-018-04796-3.
5
Ephrin receptor A2 is a functional entry receptor for Epstein-Barr virus.
Nat Microbiol. 2018 Feb;3(2):172-180. doi: 10.1038/s41564-017-0081-7. Epub 2018 Jan 1.
6
7
Divergent tropism of HHV-6A and HHV-6B in T cells expressing different CD46 isoform patterns.
Virology. 2017 Feb;502:160-170. doi: 10.1016/j.virol.2016.12.027. Epub 2017 Jan 2.
9
Clients and Oncogenic Roles of Molecular Chaperone gp96/grp94.
Curr Top Med Chem. 2016;16(25):2765-78. doi: 10.2174/1568026616666160413141613.
10
RNASEK is required for internalization of diverse acid-dependent viruses.
Proc Natl Acad Sci U S A. 2015 Jun 23;112(25):7797-802. doi: 10.1073/pnas.1424098112. Epub 2015 Jun 8.

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