Selective inactivation of CCR5 and decreased infectivity of R5 HIV-1 strains mediated by opioid-induced heterologous desensitization

J Leukoc Biol. 2003 Dec;74(6):1074-82. doi: 10.1189/jlb.0203067. Epub 2003 Sep 12.

Abstract

The opiates are well-established immunomodulatory factors, and recent evidence suggests that mu- and delta-opioid receptor ligands alter chemokine-driven chemotactic responses through the process of heterologous desensitization. In the present report, we sought to examine the capacity of mu- and delta-opioids to modulate the function of chemokine receptors CCR5 and CXCR4, the two major human immunodeficiency virus (HIV) coreceptors. We found that the chemotactic responses to the CCR1/5 ligand CCL5/regulated on activation, normal T expressed and secreted, but not the CXCR4 ligand stromal cell-derived factor-1alpha/CXCL12 were inhibited following opioid pretreatment. Studies were performed with primary monocytes and Chinese hamster ovary cells transfected with CCR5 and the micro-opioid receptor to determine whether cross-desensitization of CCR5 was a result of receptor internalization. Using radiolabeled-binding analysis, flow cytometry, and confocal microscopy, we found that the heterologous desensitization of CCR5 was not associated with a significant degree of receptor internalization. Despite this, we found that the cross-desensitization of CCR5 by opioids was associated with a decrease in susceptibility to R5 but not X4 strains of HIV-1. Our findings are consistent with the notion that impairment of the normal signaling activity of CCR5 inhibits HIV-1 coreceptor function. These results have significant implications for our understanding of the effect of opioids on the regulation of leukocyte trafficking in inflammatory disease states and the process of coreceptor-dependent HIV-1 infection. The interference with HIV-1 uptake by heterologous desensitization of CCR5 suggests that HIV-1 interaction with this receptor is not passive but involves a signal transduction process.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acquired Immunodeficiency Syndrome / prevention & control
  • Animals
  • CHO Cells
  • Calcium / metabolism
  • Chemokine CXCL12
  • Chemokines, CXC / metabolism
  • Chemotaxis
  • Cricetinae
  • Desensitization, Immunologic
  • Disease Susceptibility
  • HIV Core Protein p24 / genetics
  • HIV Long Terminal Repeat
  • HIV-1 / physiology*
  • Humans
  • Jurkat Cells
  • Monocytes / metabolism
  • Receptors, CCR5 / genetics
  • Receptors, CCR5 / metabolism*
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism
  • Receptors, Opioid, delta / physiology
  • Receptors, Opioid, mu / physiology
  • Signal Transduction
  • Transfection
  • Virus Replication / drug effects
  • Virus Replication / physiology*

Substances

  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines, CXC
  • HIV Core Protein p24
  • Receptors, CCR5
  • Receptors, CXCR4
  • Receptors, Opioid, delta
  • Receptors, Opioid, mu
  • Calcium