Microglia express CCR5, CXCR4, and CCR3, but of these, CCR5 is the principal coreceptor for human immunodeficiency virus type 1 dementia isolates

被引:235
作者
Albright, AV
Shieh, JTC
Itoh, T
Lee, B
Pleasure, D
O'Connor, MJ
Doms, RW
González-Scarano, F
机构
[1] Univ Penn, Sch Med, Dept Neurol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA
[5] Thomas Jefferson Univ, Sch Med, Dept Neurosurg, Philadelphia, PA 19107 USA
关键词
D O I
10.1128/JVI.73.1.205-213.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Microglia are the main human immunodeficiency virus (HIV) reservoir in the central nervous system and most likely play a major role in the development of HIV dementia (HIVD). To characterize human adult microglial chemokine receptors, we analyzed the expression and calcium signaling of CCR5, CCR3, and CXCR4 and their roles in HIV entry. Microglia expressed higher levels of CCR5 than of either CCR3 or CXCR4. Of these three chemokine receptors, only CCR5 and CXCR4 were able to transduce a signal in microglia in response to their respective ligands, MIP-1 beta and SDF-1 alpha, as recorded by single-cell calcium flux experiments. We also found that CCR5 is the predominant coreceptor used for infection of human adult microglia by the HIV type 1 dementia isolates HIV-1(DS-br), HIV-1(RC-br), and HIV-1(YU-2), since the anti-CCR5 antibody 2D7 was able to dramatically inhibit microglial infection by both wild-type and single-round luciferase pseudotype reporter viruses. Anti-CCR3 (7B11) and anti-CXCR4 (12G5) antibodies had little or no effect on infection. Last, we found that virus pseudotyped with the DS-br and RC-br envelopes can infect cells transfected with CD4 in conjunction with the G-protein-coupled receptors APJ, CCR8, and GPR15, which have been previously implicated in HIV entry.
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页码:205 / 213
页数:9
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