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GRP78,一种新型的新冠病毒宿主因子:其在与代谢风险因素相关的新冠肺炎中的新作用

GRP78, a Novel Host Factor for SARS-CoV-2: The Emerging Roles in COVID-19 Related to Metabolic Risk Factors.

作者信息

Shin Jihoon, Toyoda Shinichiro, Fukuhara Atsunori, Shimomura Iichiro

机构信息

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871, Japan.

Department of Diabetes Care Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

Biomedicines. 2022 Aug 17;10(8):1995. doi: 10.3390/biomedicines10081995.

Abstract

The outbreak of coronavirus disease 19 (COVID-19), caused by the infection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in an unprecedented amount of infection cases and deaths, leading to the global health crisis. Despite many research efforts, our understanding of COVID-19 remains elusive. Recent studies have suggested that cell surface glucose-regulated protein 78 (GRP78) acts as a host co-receptor for SARS-CoV-2 infection and is related to COVID-19 risks, such as older age, obesity, and diabetes. Given its significance in a wide range of biological processes, such as protein homeostasis and cellular signaling, GRP78 might also play an important role in various stages of the viral life cycle and pathology of SARS-CoV-2. In this perspective, we explore the emerging and potential roles of GRP78 in SARS-CoV-2 infection. Additionally, we discuss the association with COVID-19 risks and symptoms. We hope this review article will be helpful to understand COVID-19 pathology and promote attention and study of GRP78 from many clinical and basic research fields.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染引起的新型冠状病毒肺炎(COVID-19)疫情,已导致前所未有的感染病例和死亡人数,引发了全球健康危机。尽管进行了许多研究,但我们对COVID-19的了解仍然有限。最近的研究表明,细胞表面葡萄糖调节蛋白78(GRP78)作为SARS-CoV-2感染的宿主共受体,与COVID-19风险相关,如老年、肥胖和糖尿病。鉴于其在蛋白质稳态和细胞信号传导等广泛生物学过程中的重要性,GRP78可能在SARS-CoV-2病毒生命周期和病理学的各个阶段也发挥重要作用。从这个角度出发,我们探讨GRP78在SARS-CoV-2感染中新兴的和潜在的作用。此外,我们讨论其与COVID-19风险和症状的关联。我们希望这篇综述文章将有助于理解COVID-19病理学,并促进许多临床和基础研究领域对GRP78的关注和研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c0a/9406123/a1ac74b0a279/biomedicines-10-01995-g001.jpg

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