Astrocytes contacting HIV-1-infected macrophages increase the release of CCL2 in response to the HIV-1-dependent enhancement of membrane-associated TNFα in macrophages

Glia. 2010 Dec;58(16):1893-904. doi: 10.1002/glia.21059.

Abstract

The presence of human immunodeficiency virus (HIV)-infected macrophages in the parenchyma of central nervous system is an hallmark of acquired immunodeficiency syndrome-related neuroinflammation. Once penetrated the blood-brain barrier (BBB), macrophages closely interact with astrocytes, beginning with those lying beneath the BBB endothelium. By investigating the consequences of the cell-cell interaction between HIV-infected macrophages and astrocytes, we observed that the HIV-1 expression in macrophagic cells correlated with increased chemotactic activity in supernatants of astroglial cells. Gene array analysis revealed an impressive increase in the transcription of the gene for the CCL2/MCP-1 chemokine in astroglial cells isolated from HIV-1-infected co-cultures compared with cells from uninfected co-cultures. This phenomenon coupled with the increase in CCL2 release and depended on the cell-cell contact. In addition, it was a consequence of the HIV-1-induced enhancement of membrane-associated tumor necrosis factor-α in macrophagic cells, and correlated with increased levels of nuclear factor kappaB activation in astroglial cells. These observations could mirror a mechanism of recruitment of leukocytes through the BBB, likely contributing to the increase in both viral load and inflammation in central nervous system of HIV-infected patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Astrocytes / immunology
  • Astrocytes / pathology
  • Astrocytes / virology*
  • Astrocytoma
  • Brain Neoplasms
  • Cell Communication / immunology
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / immunology*
  • Chemotaxis / immunology
  • Coculture Techniques
  • Gene Expression / immunology
  • HIV Infections / immunology*
  • HIV Infections / pathology
  • HIV-1*
  • Humans
  • I-kappa B Proteins / metabolism
  • Macrophages / immunology
  • Macrophages / pathology
  • Macrophages / virology*
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism
  • NF-KappaB Inhibitor alpha
  • Oligonucleotide Array Sequence Analysis
  • Tumor Necrosis Factor-alpha / immunology*
  • Tumor Necrosis Factor-alpha / metabolism
  • U937 Cells

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • I-kappa B Proteins
  • Membrane Proteins
  • NFKBIA protein, human
  • Tumor Necrosis Factor-alpha
  • NF-KappaB Inhibitor alpha