Literature DB >> 23911867

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

Xiqian Lan1, Kang Cheng, Nirupama Chandel, Rivka Lederman, Aakash Jhaveri, Mohammad Husain, Ashwani Malhotra, Pravin C Singhal.   

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 H(2)O(2) 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.

Entities:  

Keywords:  HIF-1α; Jurkat cells; LTR; ROS; antioxidants; enzymes; receptors

Mesh:

Substances:

Year:  2013        PMID: 23911867      PMCID: PMC3774843          DOI: 10.1189/jlb.0313142

Source DB:  PubMed          Journal:  J Leukoc Biol        ISSN: 0741-5400            Impact factor:   4.962


  57 in total

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