Interleukin-2 inhibits HIV-1 replication in some human T cell lymphotrophic virus-1-infected cell lines via the induction and incorporation of APOBEC3G into the virion

J Biol Chem. 2013 Jun 14;288(24):17812-22. doi: 10.1074/jbc.M113.468975. Epub 2013 May 2.

Abstract

IL-2 has been used in culture of primary T cells to maintain cell proliferation. We have previously reported that IL-27 inhibits HIV-1 replication in primary T cells in the presence of IL-2. To gain a better understanding of the mechanisms involved in this inhibitory effect, we attempted to investigate in detail the effects of IL-27 and IL-2 using several cell lines. Unexpectedly, IL-27 did not inhibit HIV-1 in T cell lines, whereas IL-2 inhibited HIV-1 replication in the human T cell lymphotrophic virus (HTLV)-1-transformed T cell lines, MT-2, MT-4, SLB-1, and ATL-2. No effects were seen in HTLV-1-negative cell lines. Utilizing MT-2 cells, we demonstrated that IL-2 treatment inhibited HIV-1 syncytia-inducing ability and dose-dependently decreased supernatant p24 antigen levels by >90%. Using real time PCR and Western blot analysis, we observed that IL-2 treatment induced the host restriction factor, APOBEC3G with accumulation into the lower molecular mass active form as characterized by FPLC. Further analysis revealed that the virus recovered from IL-2-treated MT-2 cells had impaired replication competency. This was found to be due to incorporation of APOBEC3G into the virion despite the presence of Vif. These findings demonstrate a novel role for IL-2 in regulating production of infectious HIV-1 virions in HTLV-1-infected cells through the induction of APOBEC3G.

Keywords: Cytokine; Gamma Chain Cytokines; HIV-1; HTLV-1; Host Defense; Host Restriction Factors; IL-2; Immunology; Interleukin; Viral Replication.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • APOBEC-3G Deaminase
  • CD4 Antigens / metabolism
  • Cell Line
  • Cytidine Deaminase / genetics*
  • Cytidine Deaminase / metabolism
  • Enzyme Induction
  • Gene Knockdown Techniques
  • HIV-1 / physiology*
  • Humans
  • Interleukin-2 / physiology*
  • Mutation
  • RNA, Small Interfering / genetics
  • Receptors, CXCR4 / metabolism
  • Reverse Transcription
  • Sequence Analysis, DNA
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / virology*
  • Transcriptional Activation
  • Virus Replication*

Substances

  • CD4 Antigens
  • CXCR4 protein, human
  • Interleukin-2
  • RNA, Small Interfering
  • Receptors, CXCR4
  • APOBEC-3G Deaminase
  • APOBEC3G protein, human
  • Cytidine Deaminase