Jinno A, Shimizu N, Soda Y, Haraguchi Y, Kitamura T, Hoshino H
Department of Hygiene and Virology, Gunma University School of Medicine, Japan.
Biochem Biophys Res Commun. 1998 Feb 13;243(2):497-502. doi: 10.1006/bbrc.1998.8130.
We have isolated HIV-1 variants that infect brain-derived CD4-positive cells, which are resistant to both macrophage (M)-tropic and T-cell line (T)-tropic HIV-1 strains. It is possible that this brain cell tropism of the HIV-1 variants is determined by the interaction of HIV-1 with a chemokine receptor (CKR) gene. We attempted to detect the expression of the CKR-like genes using degenerate PCR primers. The brain-derived cells expressed a CKR-like gene TER1/CCR8. Human CD4-expressing cells resistant to all HIV-1 strains became susceptible to brain-cell tropic HIV-1 variants after expression of TER1 in these cells, but these cells were still resistant to M-tropic strains or T-tropic IIIB strain. TER1 was expressed in brain-derived cells and human T-cells. These findings suggest that TER1/CCR8 functions as a co-receptor for HIV-1 infection for brain-derived cells as well as T cells.
我们已经分离出感染脑源性CD4阳性细胞的HIV-1变体,这些细胞对巨噬细胞(M)嗜性和T细胞系(T)嗜性的HIV-1毒株均具有抗性。HIV-1变体的这种脑细胞嗜性可能是由HIV-1与趋化因子受体(CKR)基因的相互作用所决定的。我们试图使用简并PCR引物检测CKR样基因的表达。脑源性细胞表达一种CKR样基因TER1/CCR8。对所有HIV-1毒株均具有抗性的人CD4表达细胞在这些细胞中表达TER1后,变得易受脑细胞嗜性HIV-1变体的感染,但这些细胞对M嗜性毒株或T嗜性IIIB毒株仍具有抗性。TER1在脑源性细胞和人T细胞中表达。这些发现表明,TER1/CCR8作为HIV-1感染脑源性细胞和T细胞的共受体发挥作用。