High glucose enhances HIV entry into T cells through upregulation of CXCR4

  • Xiqian Lan
  • , Kang Cheng
  • , Nirupama Chandel
  • , Rivka Lederman
  • , Aakash Jhaveri
  • , Mohammad Husain
  • , Ashwani Malhotra
  • , Pravin C. Singhal

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

It is well known that patients with HIV are prone to diabetes mellitus because of the side effects of HARRT. However, whether high glucose affects the HIV infection of T cells is not clear. Recent studies have shown that upregulation of GLUT-1 renders T cells susceptible to HIV infection. We hypothesized that hyperglycemia has the potential to increase HIV infection by enhancing its entry into immune cells. The effect of high glucose on HIV entry into T cells (Jurkat cells and PBMCs) and the mechanisms involved were investigated. High glucose significantly enhanced HIV entry, which was associated with increased T-cell expression of CXCR4. However, T cells with silenced HIF-1α displayed attenuated expression of CXCR4, whereas T cells with silenced CXCR4 showed decreased HIV entry in a high-glucose milieu. On the one hand, high glucose stimulated T-cell ROS generation, and H2O2 at low concentrations enhanced the entry of HIV into T cells. On the other hand, inhibition of ROS not only attenuated high-glucose-mediated T-cell expression of CXCR4 and HIF-1α but also mitigated T-cell HIV entry in a high-glucose milieu. In our study, high glucose enhanced HIV entry into T cells by increasing expression of CXCR4 and HIF-1α.

Original languageEnglish
Pages (from-to)769-777
Number of pages9
JournalJournal of Leukocyte Biology
Volume94
Issue number4
DOIs
StatePublished - Oct 2013
Externally publishedYes

Keywords

  • Antioxidants
  • Enzymes
  • HIF-1α
  • Jurkat cells
  • LTR
  • ROS
  • Receptors

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