Neil Stuart J D, Aasa-Chapman Marlen M I, Clapham Paul R, Nibbs Robert J, McKnight Aine, Weiss Robin A
Wohl Virion Centre, Division of Infection and Immunity, University College London, UK.
J Virol. 2005 Aug;79(15):9618-24. doi: 10.1128/JVI.79.15.9618-9624.2005.
The role of coreceptors other than CCR5 and CXCR4 in the pathogenesis of human immunodeficiency virus (HIV) disease is controversial. Here we show that a promiscuous CC chemokine receptor, D6, can function as a coreceptor for various primary dual-tropic isolates of HIV type 1 (HIV-1) and HIV-2. Furthermore, D6 usage is common among chimeric HIV-1 constructs bearing the gp120 proteins of isolates from early seroconverting patients. D6 mRNA and immunoreactivity were demonstrated to be expressed in HIV-1 target cells such as macrophages, peripheral blood mononuclear cells, and primary astrocytes. In primary astrocytes, an RNA interference-mediated knockdown of D6 expression inhibited D6-tropic isolate infection. D6 usage may account for some previous observations of alternative receptor tropism for primary human cells. Thus, D6 may be an important receptor for HIV pathogenesis in the brain and for the early dissemination of virus in the host.
除CCR5和CXCR4之外的共受体在人类免疫缺陷病毒(HIV)疾病发病机制中的作用存在争议。在此我们表明,一种具有广泛活性的CC趋化因子受体D6可作为1型人类免疫缺陷病毒(HIV-1)和HIV-2各种原发性双嗜性分离株的共受体。此外,在携带早期血清转化患者分离株的gp120蛋白的嵌合HIV-1构建体中,D6的使用很常见。D6 mRNA和免疫反应性在HIV-1靶细胞如巨噬细胞、外周血单核细胞和原代星形胶质细胞中表达。在原代星形胶质细胞中,RNA干扰介导的D6表达敲低抑制了D6嗜性分离株的感染。D6的使用可能解释了之前关于原代人类细胞替代受体嗜性的一些观察结果。因此,D6可能是HIV在大脑发病机制以及病毒在宿主体内早期传播中的重要受体。