Human herpesvirus 7 open reading frame U12 encodes a functional β-chemokine receptor

被引:38
作者
Nakano, K
Tadagaki, K
Isegawa, Y
Aye, MM
Zou, P
Yamanishi, K
机构
[1] Osaka Univ, Sch Med, Dept Microbiol C1, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Div Adv Med Bacteriol G5, Suita, Osaka 5650871, Japan
[3] Hyogo Med Univ, Dept Microbiol, Nishinomiya, Hyogo, Japan
[4] Inst Med, Dept Microbiol, Yangon, Myanmar
关键词
D O I
10.1128/JVI.77.14.8108-8115.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human herpesvirus 7 (HHV-7), which belongs to the betaherpesvirus subfamily, infects mainly CD4(+) T cells in vitro and infects children during infancy. After the primary infection, HHV-7 becomes latent. HHV-7 contains two genes (U12 and U51) that encode putative homologs of cellular G-protein-coupled receptors. To analyze the biological function of the U12 gene, we cloned the gene and expressed the U12 protein in cells. The U12 gene encoded a calcium-mobilizing receptor for the EBI1 ligand chemokine-macrophage inflammatory protein 3beta (ELC/MIP-3beta) but not for other chemokines, suggesting that the chemokine selectivity of the U12 gene product is distinct from that of the known mammalian chemokine receptors. These studies revealed that U12 activates distinct transmembrane signaling pathways that may mediate biological functions by binding with a beta-chemokine, ELC/MIP-3beta.
引用
收藏
页码:8108 / 8115
页数:8
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