miR-146a controls CXCR4 expression in a pathway that involves PLZF and can be used to inhibit HIV-1 infection of CD4+ T lymphocytes

被引:26
作者
Quaranta, Maria Teresa [1 ]
Olivetta, Eleonora [2 ]
Sanchez, Massimo [3 ]
Spinello, Isabella [1 ]
Paolillo, Rosa [1 ]
Arenaccio, Claudia [2 ,4 ]
Federico, Maurizio [2 ]
Labbaye, Catherine [1 ]
机构
[1] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[2] Ist Super Sanita, Natl AIDS Ctr, I-00161 Rome, Italy
[3] Ist Super Sanita, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
[4] Univ Roma Tre, Dept Sci, Rome, Italy
关键词
HIV-1; PLZF; miR-146a; CXCR4; CD4(+) T lymphocytes; U937; cells; CHEMOKINE RECEPTOR; PROGENITOR CELLS; MICRORNAS; VIRUS; ENTRY; CANCER; TRANSCRIPTION; REPLICATION; MACROPHAGES; DEFENSE;
D O I
10.1016/j.virol.2015.01.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
MicroRNA miR-146a and PLZF are reported as major players in the control of hematopoiesis, immune function and cancer. PLZF is described as a miR-146a repressor, whereas CXCR4 and TRAF6 were identified as miR-146a direct targets in different cell types. CXCR4 is a co-receptor of CD4 molecule that facilitates HIV-1 entry into T lymphocytes and myeloid cells, whereas TRAF6 is involved in immune response. Thus, the role of miR-146a in HIV-1 infection is currently being thoroughly investigated. In this study, we found that PLZF mediates suppression of miR-146a to control increases of CXCR4 and TRAF6 protein levels in human primary CD4(+) T lymphocytes. We show that miR-146a upregulation by AMD3100 treatment or PLZF silencing, decreases CXCR4 protein expression and prevents HIV-1 infection of leukemic monocytic cell line and CD4(+) T lymphocytes. Our findings improve the prospects of developing new therapeutic strategies to prevent HIV-1 entry via CXCR4 by using the PLZF/miR-146a axis. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:27 / 38
页数:12
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