Gabuzda D, He J, Ohagen A, Vallat A V
Division of Human Retrovirology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA, 02115, USA.
Semin Immunol. 1998 Jun;10(3):203-13. doi: 10.1006/smim.1998.0133.
Several members of the chemokine receptor are used as coreceptors for HIV-1 infection in the central nervous system (CNS). CCR5 and CCR3 are coreceptors together with CD4 for HIV-1 infection of microglia, the major target for HIV-1 infection in the CNS. Microglia express CXCR4, but their infection by HIV-1 viruses that use only CXCR4 as a coreceptor is relatively inefficient. CXCR4 is also expressed in subpopulations of neurons that are resistant to HIV-1 infection. Additional orphan chemokine receptors that can mediate HIV-1 or SIV entry are expressed in the brain or neurally-derived cell lines, but their role in CNS infection has not been defined. The pattern of chemokine receptor expression in the brain is likely to determine the tropism of HIV-1 for particular CNS target cells and to impact inflammatory and degenerative mechanisms associated with CNS infection.
趋化因子受体的几个成员被用作人类免疫缺陷病毒1型(HIV-1)在中枢神经系统(CNS)感染的共受体。CCR5和CCR3是HIV-1感染小胶质细胞(CNS中HIV-1感染的主要靶细胞)时与CD4共同作用的共受体。小胶质细胞表达CXCR4,但它们被仅使用CXCR4作为共受体的HIV-1病毒感染的效率相对较低。CXCR4也在对HIV-1感染具有抗性的神经元亚群中表达。其他能够介导HIV-1或猴免疫缺陷病毒(SIV)进入的孤儿趋化因子受体在大脑或神经源性细胞系中表达,但其在CNS感染中的作用尚未明确。大脑中趋化因子受体的表达模式可能决定HIV-1对特定CNS靶细胞的嗜性,并影响与CNS感染相关的炎症和退化机制。