Sharma-Walia Neelam, Naranatt Pramod P, Krishnan Harinivas H, Zeng Ling, Chandran Bala
Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
J Virol. 2004 Apr;78(8):4207-23. doi: 10.1128/jvi.78.8.4207-4223.2004.
Human herpesvirus 8 (HHV-8; Kaposi's sarcoma-associated herpesvirus) envelope glycoprotein gB possesses an RGD motif, interacts with alpha 3 beta 1 integrin, and uses it as one of the entry receptors. HHV-8 induces the integrin-dependent focal adhesion kinase (FAK), a critical step in the outside-in signaling pathways necessary for the subsequent phosphorylation of other cellular kinases, cytoskeletal rearrangements, and other functions. As an initial step toward deciphering the role of HHV-8 gB-integrin interaction in infection, signal pathways induced by gB were examined. A truncated form of gB without the transmembrane and carboxyl domains (gB Delta TM), a gB Delta TM mutant form (gB Delta TM-RGA) with an RGD-to-RGA mutation, and inhibitors of cellular kinases were used. HHV-8 gB Delta TM, but not gB Delta TM-RGA, induced FAK phosphorylation in target cells, which was in part dependent on the presence of alpha 3 beta 1 integrin. FAK was critical for the subsequent phosphorylation of Src by gB Delta TM, and Src induction was essential for the phosphorylation of phosphatidylinositol 3-kinase (PI-3K). HHV-8 gB Delta TM-induced PI-3K was essential for the induction of RhoA and Cdc42 Rho GTPases that was accompanied by the cytoskeletal rearrangements. These gB-induced morphological changes were inhibited by the PI-3K inhibitors. Ezrin, one of the essential elements required to cross-link the actin cytoskeleton with the plasma membrane and to induce the morphological changes, was induced by the Rho GTPases. Inhibition of cellular tyrosine kinases by the brief treatment of cells with 4',5,7-trihydroxyisoflavone (genistein) blocked the entry of HHV-8 into target cells. These findings suggest that, independently of other viral glycoproteins and via its RGD motif, HHV-8 gB induces integrin-dependent pre-existing FAK-Src-PI-3K-Rho GTPase kinases. Since these signal pathways play vital roles in host cell endocytosis and movement of particulate materials in the cytoplasm, the early stages of HHV-8 gB interaction with host cells may provide a very conducive environment for the successful infection of target cells.
人类疱疹病毒8型(HHV - 8;卡波西肉瘤相关疱疹病毒)包膜糖蛋白gB具有一个RGD基序,可与α3β1整合素相互作用,并将其用作一种进入受体。HHV - 8诱导整合素依赖性粘着斑激酶(FAK),这是外向内信号通路中的关键步骤,对于随后其他细胞激酶的磷酸化、细胞骨架重排及其他功能而言必不可少。作为解读HHV - 8 gB - 整合素相互作用在感染中作用的第一步,研究了gB诱导的信号通路。使用了一种不含跨膜和羧基结构域的gB截短形式(gBΔTM)、一种具有RGD到RGA突变的gBΔTM突变形式(gBΔTM - RGA)以及细胞激酶抑制剂。HHV - 8 gBΔTM而非gBΔTM - RGA在靶细胞中诱导FAK磷酸化,这部分依赖于α3β1整合素的存在。FAK对于随后gBΔTM诱导的Src磷酸化至关重要,而Src的诱导对于磷脂酰肌醇3 - 激酶(PI - 3K)的磷酸化必不可少。HHV - 8 gBΔTM诱导的PI - 3K对于诱导RhoA和Cdc42 Rho GTP酶至关重要,这伴随着细胞骨架重排。这些gB诱导的形态变化被PI - 3K抑制剂所抑制。埃兹蛋白是将肌动蛋白细胞骨架与质膜交联并诱导形态变化所需的关键元件之一,由Rho GTP酶诱导产生。用4',5,7 - 三羟基异黄酮(染料木黄酮)短暂处理细胞以抑制细胞酪氨酸激酶,可阻断HHV - 8进入靶细胞。这些发现表明,HHV - 8 gB独立于其他病毒糖蛋白并通过其RGD基序,诱导整合素依赖性的预先存在的FAK - Src - PI - 3K - Rho GTP酶激酶。由于这些信号通路在宿主细胞内吞作用和细胞质中颗粒物质的移动中起着至关重要的作用,HHV - 8 gB与宿主细胞相互作用的早期阶段可能为靶细胞的成功感染提供非常有利的环境。