Beisser P S, Laurent L, Virelizier J L, Michelson S
Unité d'Immunologie Virale, Institut Pasteur, 75274 Paris Cedex 15, France.
J Virol. 2001 Jul;75(13):5949-57. doi: 10.1128/JVI.75.13.5949-5957.2001.
The human cytomegalovirus (HCMV) US28 gene product, pUS28, is a G protein-coupled receptor that interacts with both CC and CX(3)C chemokines. To date, the role of pUS28 in immune evasion and cell migration has been studied only in cell types that can establish productive HCMV infection. We show that HCMV can latently infect THP-1 monocytes and that during latency US28 is transcribed. We also show that the transcription is sustained during differentiation of the THP-1 monocytes. Since cells expressing pUS28 were previously shown to adhere to immobilized CX(3)C chemokines (C. A. Haskell, M. D. Cleary, and I. F. Charo, J. Biol. Chem. 275:34183-34189, 2000), we hypothesize that latently infected circulating monocytes express pUS28, thereby enabling adhesion of these cells to CX(3)C-exposing endothelium. Consequently, the US28-encoded chemokine receptor may play an important role in dissemination of latent HCMV.
人类巨细胞病毒(HCMV)的US28基因产物pUS28是一种G蛋白偶联受体,可与CC和CX(3)C趋化因子相互作用。迄今为止,仅在能够建立高效HCMV感染的细胞类型中研究了pUS28在免疫逃逸和细胞迁移中的作用。我们发现HCMV可潜伏感染THP-1单核细胞,且在潜伏期间US28会转录。我们还表明,在THP-1单核细胞分化过程中,转录持续存在。由于先前已证明表达pUS28的细胞可黏附于固定化的CX(3)C趋化因子(C. A. Haskell、M. D. Cleary和I. F. Charo,《生物化学杂志》275:34183 - 34189,2000年),我们推测潜伏感染的循环单核细胞表达pUS28,从而使这些细胞能够黏附于暴露CX(3)C的内皮细胞。因此,US28编码的趋化因子受体可能在潜伏性HCMV的传播中发挥重要作用。