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Human cytomegalovirus infection reduces surface CCR5 expression in human microglial cells, astrocytes and monocyte-derived macrophages.
- Source :
-
Microbes and infection [Microbes Infect] 2002 Nov; Vol. 4 (14), pp. 1401-8. - Publication Year :
- 2002
-
Abstract
- Within the brain, glial cells are target cells for human cytomegalovirus (HCMV) and HIV. We infected cultures of unstimulated human microglial cells and astrocytes of embryonic origin and of monocyte-derived macrophages (MDM) with HCMV strain AD169 and observed down-regulation of the plasma membrane expression of CCR5 in the three cell types, and of CXCR4 and CD4 in microglial cells only. Cells were then coinfected simultaneously or at a 24-h interval with both AD169 and two different HIV-1 monocytotropic strains. HCMV late antigens and HIV-1 tat protein colocalized in the cytoplasm of 5-10% of microglia and MDM. p24 antigen levels decreased 10- to 40-fold in supernatants of MDM and the reduction was greater when HCMV infection was performed 24 h before HIV-1 infection. These data suggest that HCMV-induced reduction in the cell-surface expression of the primary co-receptor of HIV-1 monocytotropic strains may impair the ability of HIV to infect these cells.
- Subjects :
- Antigens, Viral analysis
Astrocytes metabolism
CD4 Antigens immunology
CD4 Antigens metabolism
Cells, Cultured
Chemokine CCL4
Chemokine CCL5 analysis
Cytomegalovirus growth & development
Cytomegalovirus Infections metabolism
HIV Core Protein p24 analysis
HIV-1 growth & development
HIV-1 metabolism
Humans
Macrophage Inflammatory Proteins analysis
Macrophages metabolism
Microglia metabolism
Monocytes cytology
Monocytes physiology
Receptors, CCR5 immunology
Receptors, CXCR4 immunology
Receptors, CXCR4 metabolism
Receptors, Chemokine genetics
Receptors, Chemokine metabolism
Viral Proteins genetics
Viral Proteins metabolism
Virus Replication
Astrocytes virology
Cytomegalovirus physiology
Macrophages virology
Microglia virology
Receptors, CCR5 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1286-4579
- Volume :
- 4
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Microbes and infection
- Publication Type :
- Academic Journal
- Accession number :
- 12475630
- Full Text :
- https://doi.org/10.1016/s1286-4579(02)00022-9