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Research Article Free access | 10.1172/JCI4461
Division of Molecular Medicine, Department of Medicine, Cornell University Medical College and The New York Hospital, New York 10021, USA. mcgersh@mail.med.cornell.edu
Find articles by Gershengorn, M. in: JCI | PubMed | Google Scholar
Division of Molecular Medicine, Department of Medicine, Cornell University Medical College and The New York Hospital, New York 10021, USA. mcgersh@mail.med.cornell.edu
Find articles by Geras-Raaka, E. in: JCI | PubMed | Google Scholar
Division of Molecular Medicine, Department of Medicine, Cornell University Medical College and The New York Hospital, New York 10021, USA. mcgersh@mail.med.cornell.edu
Find articles by Varma, A. in: JCI | PubMed | Google Scholar
Division of Molecular Medicine, Department of Medicine, Cornell University Medical College and The New York Hospital, New York 10021, USA. mcgersh@mail.med.cornell.edu
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Published October 15, 1998 - More info
Kaposi's sarcoma-associated herpesvirus (KSHV)/human herpesvirus 8, a virus that appears to be involved in the pathogenesis of Kaposi's sarcoma and primary effusion lymphomas, encodes a G protein-coupled receptor (KSHV-GPCR) that exhibits constitutive signaling. In this report, we show that two chemokines, interleukin 8 (IL-8) and growth-related protein-alpha, activate KSHV-GPCR over constitutive levels. Moreover, as with human receptors, the integrity of the ELR motif of these chemokines is required for activation of KSHV-GPCR. Other residues that are required for IL-8 binding to human chemokine receptors CXCR1 and CXCR2 are important for KSHV-GPCR activation also. Thus, it appears that the ELR binding site and other key domains of ELR chemokine activation have been preserved in the virus KSHV-GPCR. The results suggest that KSHV-GPCR originated from CXCR1 or CXCR2 and that activation of KSHV-GPCR by endogenous chemokines may affect the pathobiology of KSHV infection in humans.