Toll-like receptor 3 signalling up-regulates expression of the HIV co-receptor G-protein coupled receptor 15 on human CD4+ T cells

PLoS One. 2014 Feb 18;9(2):e88195. doi: 10.1371/journal.pone.0088195. eCollection 2014.

Abstract

Background: Many HIV-2 and SIV isolates, as well as some HIV-1 strains, can use the orphan 7-transmembrane receptor GPR15 as co-receptor for efficient entry into host cells. GPR15 is expressed on central memory and effector memory CD4(+) T cells in healthy individuals and a subset of these cells is susceptible to HIV-1 and SIV infection. However, it has not been determined whether GPR15 expression is altered in the context of HIV-1 infection.

Results: Here, we show that GPR15 expression in CD4(+) T cells is markedly up-regulated in some HIV-1 infected individuals compared to the rest of the infected patients and to healthy controls. Infection of the PM1 T cell line with primary HIV-1 isolates was found to up-regulate GPR15 expression on the infected cells, indicating that viral components can induce GPR15 expression. Up-regulation of GPR15 expression on CD4(+) T cells was induced by activation of Toll-like receptor 3 signalling via TIR-domain-containing adapter-inducing interferon-β (TRIF) and was more prominent on gut-homing compared to lymph node-homing CD4(+) T cells.

Conclusion: These results suggest that infection-induced up-regulation of GPR15 expression could increase susceptibility of CD4(+) T cells to HIV infection and target cell availability in the gut in some infected individuals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD19 / metabolism
  • Biopsy
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / virology*
  • CD8-Positive T-Lymphocytes / cytology
  • Cell Separation
  • Colon / metabolism
  • Colon / pathology
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV-1 / metabolism*
  • Humans
  • Immunologic Memory
  • Leukocytes, Mononuclear / cytology
  • Male
  • Middle Aged
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, Peptide / metabolism*
  • Signal Transduction
  • Toll-Like Receptor 3 / metabolism*
  • Up-Regulation

Substances

  • Antigens, CD19
  • GPR15 protein, human
  • Receptors, G-Protein-Coupled
  • Receptors, Peptide
  • TLR3 protein, human
  • Toll-Like Receptor 3

Grants and funding

This work is supported by the International Research Training Group 1273 (MK) and by the Swedish Medical Research Council. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.