1. Academic Validation
  2. Interferon-inducible LY6E Protein Promotes HIV-1 Infection

Interferon-inducible LY6E Protein Promotes HIV-1 Infection

  • J Biol Chem. 2017 Mar 17;292(11):4674-4685. doi: 10.1074/jbc.M116.755819.
Jingyou Yu 1 2 Chen Liang 3 4 Shan-Lu Liu 5 6
Affiliations

Affiliations

  • 1 From the Center for Retrovirus Research.
  • 2 Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210.
  • 3 the McGill AIDS Centre, Lady Davis Institute, Montreal, Quebec H3T 1E2, Canada, and.
  • 4 the Department of Microbiology and Immunology, McGill University, Montreal, Quebec H3A 2B4, Canada.
  • 5 From the Center for Retrovirus Research, liu.6244@osu.edu.
  • 6 Center for Microbial Interface Biology, and.
Abstract

LY6E is a glycosylphosphatidylinositol-anchored, IFN-inducible protein that regulates T lymphocytes proliferation, differentiation, and development. Single-nucleotide polymorphism rs2572886 in the LY6 family protein locus has been shown to associate with accelerated progression to AIDS. In this study, we show that LY6E promotes HIV, type 1 (HIV-1) Infection by enhancing viral entry and gene expression. Knockdown of LY6E in human peripheral blood mononuclear, SupT1, and THP-1 cells diminishes HIV-1 replication. Virion-cell and cell-cell fusion experiments revealed that LY6E promotes membrane fusion of the viral entry step. Interestingly, we find that LTR-driven HIV-1 gene expression is also enhanced by LY6E, suggesting additional roles of LY6E in HIV-1 replication. HIV-1 Infection induces LY6E expression in human peripheral blood mononuclear cells, concomitant with increased production of type I IFN and some classical IFN-stimulated genes. Altogether, our results demonstrate that IFN-inducible LY6E promotes HIV-1 entry and replication and highlight a positive regulatory role of IFN-induced proteins in HIV-1 Infection. Our work emphasizes the complexity of IFN-mediated signaling in HIV-host interaction and AIDS pathogenesis.

Keywords

HIV; IFN-stimulated genes; LY6E; gene expression; lymphocyte; membrane fusion; virus entry.

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