Parry C M, Simas J P, Smith V P, Stewart C A, Minson A C, Efstathiou S, Alcami A
Division of Virology, Department of Pathology, University of Cambridge, Cambridge CB2 1QP, United Kingdom.
J Exp Med. 2000 Feb 7;191(3):573-8. doi: 10.1084/jem.191.3.573.
Chemokines are a family of small proteins that interact with seven-transmembrane domain receptors and modulate the migration of immune cells into sites of inflammation and infection. The murine gammaherpesvirus 68 M3 gene encodes a secreted 44-kD protein with no sequence similarity to known chemokine receptors. We show that M3 binds a broad range of chemokines, including CC, CXC, C, and CX(3)C chemokines, but does not bind human B cell-specific nor mouse neutrophil-specific CXC chemokines. This herpesvirus chemokine binding protein (hvCKBP) blocks the interaction of chemokines with high-affinity cellular receptors and inhibits chemokine-induced elevation of intracellular calcium levels. hvCKBP is the first soluble chemokine receptor identified in herpesviruses; it represents a novel protein structure with the ability to bind all subfamilies of chemokines in solution and has potential therapeutic applications.
趋化因子是一类小蛋白质,它们与七跨膜结构域受体相互作用,并调节免疫细胞向炎症和感染部位的迁移。鼠γ疱疹病毒68 M3基因编码一种分泌型44-kD蛋白,与已知趋化因子受体无序列相似性。我们发现M3可结合多种趋化因子,包括CC、CXC、C和CX(3)C趋化因子,但不结合人B细胞特异性或小鼠中性粒细胞特异性CXC趋化因子。这种疱疹病毒趋化因子结合蛋白(hvCKBP)可阻断趋化因子与高亲和力细胞受体的相互作用,并抑制趋化因子诱导的细胞内钙水平升高。hvCKBP是疱疹病毒中鉴定出的首个可溶性趋化因子受体;它代表一种新型蛋白质结构,能够在溶液中结合趋化因子的所有亚家族,并具有潜在的治疗应用价值。