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http://purl.uniprot.org/citations/12584338http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12584338http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12584338http://www.w3.org/2000/01/rdf-schema#comment"Human herpesvirus 8 (HHV-8) or Kaposi's sarcoma-associated herpesvirus, implicated in the pathogenesis of Kaposi's sarcoma, utilizes heparan sulfate-like molecules to bind the target cells via its envelope-associated glycoproteins gB and gpK8.1A. HHV-8-gB possesses the Arg-Gly-Asp (RGD) motif, the minimal peptide region of many proteins known to interact with subsets of host cell surface integrins. HHV-8 utilizes alpha3beta1 integrin as one of the receptors for its entry into the target cells via its gB interaction and induces the activation of focal adhesion kinase (FAK) (S. M. Akula, N. P. Pramod, F.-Z. Wang, and B. Chandran, Cell 108:407-419, 2002). Since FAK activation is the first step in the outside-in signaling necessary for integrin-mediated cytoskeletal rearrangements, cell adhesions, motility, and proliferation, the ability of HHV-8-gB to mediate the target cell adhesion was examined. A truncated form of gB without the transmembrane and carboxyl domains (gBdeltaTM) and a gBdeltaTM mutant (gBdeltaTM-RGA) with a single amino acid mutation (RGD to RGA) were expressed in a baculovirus system and purified. Radiolabeled HHV-8-gBdeltaTM, gBdeltaTM-RGA, and deltaTMgpK8.1A proteins bound to the human foreskin fibroblasts (HFFs), human dermal microvascular endothelial (HMVEC-d) cells, human B (BJAB) cells, and Chinese hamster ovary (CHO-K1) cells with equal efficiency, which was blocked by preincubation of proteins with soluble heparin. Maxisorp plate-bound gBdeltaTM protein induced the adhesion of HFFs and HMVEC-d and monkey kidney epithelial (CV-1) cells in a dose-dependent manner. In contrast, the gBdeltaTM-RGA and DeltaTMgpK8.1A proteins did not mediate adhesion. Adhesion mediated by gBdeltaTM was blocked by the preincubation of target cells with RGD-containing peptides or by the preincubation of plate-bound gBdeltaTM protein with rabbit antibodies against gB peptide containing the RGD sequence. In contrast, adhesion was not blocked by the preincubation of plate-bound gBdeltaTM protein with heparin, suggesting that the adhesion is mediated by the RGD amino acids of gB, which is independent of the heparin-binding domain of gB. Integrin-ligand interaction is dependent on divalent cations. Adhesion induced by the gBdeltaTM was blocked by EDTA, thus suggesting the role of integrins in the observed adhesions. Focal adhesion components such as FAK and paxillin were activated by the binding of gBdeltaTM protein to the target cells but not by gBdeltaTM-RGA protein binding. Inhibition of FAK phosphorylation by genistein blocked gBdeltaTM-induced FAK activation and cell adhesion. These findings suggest that HHV-8-gB could mediate cell adhesion via its RGD motif interaction with the cell surface integrin molecules and indicate the induction of cellular signaling pathways, which may play roles in the infection of target cells and in Kaposi's sarcoma pathogenesis."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.org/dc/terms/identifier"doi:10.1128/jvi.77.5.3131-3147.2003"xsd:string
http://purl.uniprot.org/citations/12584338http://purl.org/dc/terms/identifier"doi:10.1128/jvi.77.5.3131-3147.2003"xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Zeng L."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Zeng L."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Akula S.M."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Akula S.M."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Chandran B."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Chandran B."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Sharma-Walia N."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Sharma-Walia N."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Wang F.Z."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/author"Wang F.Z."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/name"J. Virol."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/name"J. Virol."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/pages"3131-3147"xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/pages"3131-3147"xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/title"Human herpesvirus 8 envelope glycoprotein B mediates cell adhesion via its RGD sequence."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/title"Human herpesvirus 8 envelope glycoprotein B mediates cell adhesion via its RGD sequence."xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/volume"77"xsd:string
http://purl.uniprot.org/citations/12584338http://purl.uniprot.org/core/volume"77"xsd:string
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