Gershengorn M C, Geras-Raaka E, Varma A, Clark-Lewis I
Division of Molecular Medicine, Department of Medicine, Cornell University Medical College and The New York Hospital, New York 10021, USA.
J Clin Invest. 1998 Oct 15;102(8):1469-72. doi: 10.1172/JCI4461.
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.
卡波西肉瘤相关疱疹病毒(KSHV)/人疱疹病毒8型,一种似乎与卡波西肉瘤和原发性渗出性淋巴瘤发病机制有关的病毒,编码一种具有组成性信号传导的G蛋白偶联受体(KSHV - GPCR)。在本报告中,我们表明两种趋化因子,即白细胞介素8(IL - 8)和生长相关蛋白α,可使KSHV - GPCR的激活水平超过组成性水平。此外,与人类受体一样,这些趋化因子的ELR基序的完整性是激活KSHV - GPCR所必需的。IL - 8与人趋化因子受体CXCR1和CXCR2结合所需的其他残基对KSHV - GPCR的激活也很重要。因此,似乎ELR趋化因子激活的ELR结合位点和其他关键结构域在病毒KSHV - GPCR中得以保留。结果表明KSHV - GPCR起源于CXCR1或CXCR2,内源性趋化因子对KSHV - GPCR的激活可能会影响人类KSHV感染的病理生物学。