International Centre for Genetic Engineering and Biotechnology (ICGEB), Observatory, Cape Town 7925, South Africa.
Institute of Infectious Disease and Molecular Medicine (IDM), Faculty of Health Sciences, University of Cape Town, Observatory, Cape Town 7925, South Africa.
Viruses. 2021 Jan 17;13(1):118. doi: 10.3390/v13010118.
The process of Kaposi's Sarcoma Herpes Virus' (KSHV) entry into target cells is complex and engages several viral glycoproteins which bind to a large range of host cell surface molecules. Receptors for KSHV include heparan sulphate proteoglycans (HSPGs), several integrins and Eph receptors, cystine/glutamate antiporter (xCT) and Dendritic Cell-Specific Intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN). This diverse range of potential binding and entry sites allows KSHV to have a broad cell tropism, and entry into specific cells is dependent on the available receptor repertoire. Several molecules involved in KSHV entry have been well characterized, particularly those postulated to be associated with KSHV-associated pathologies such as Kaposi's Sarcoma (KS). In this review, KSHV infection of specific cell types pertinent to its pathogenesis will be comprehensively summarized with a focus on the specific cell surface binding and entry receptors KSHV exploits to gain access to a variety of cell types. Gaps in the current literature regarding understanding interactions between KSHV glycoproteins and cellular receptors in virus infection are identified which will lead to the development of virus infection intervention strategies.
卡波氏肉瘤疱疹病毒(KSHV)进入靶细胞的过程较为复杂,涉及几种病毒糖蛋白,这些糖蛋白与大量宿主细胞表面分子结合。KSHV 的受体包括硫酸乙酰肝素蛋白聚糖(HSPGs)、几种整合素和 Eph 受体、胱氨酸/谷氨酸反向转运体(xCT)和树突状细胞特异性细胞间黏附分子 3 抓取非整联蛋白(DC-SIGN)。这种多样化的潜在结合和进入位点使 KSHV 具有广泛的细胞嗜性,而进入特定细胞取决于可用的受体谱。已对参与 KSHV 进入的几种分子进行了很好的描述,特别是那些推测与卡波氏肉瘤(KS)等 KSHV 相关病理相关的分子。在这篇综述中,将全面总结与 KSHV 发病机制相关的特定细胞类型的 KSHV 感染,重点介绍 KSHV 利用的特定细胞表面结合和进入受体,以进入各种细胞类型。确定了当前关于理解病毒感染过程中 KSHV 糖蛋白和细胞受体之间相互作用的文献中的空白,这将导致开发病毒感染干预策略。