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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Soluble HIV-1 gp120 enhances HIV-1 replication in non-dividing CD4+T cells, mediated via cell signaling and Tat cofactor overexpression</dc:title>
  <dc:creator>/Miss&#xE9;, Doroth&#xE9;e</dc:creator>
  <dc:creator>Gajardo, J.</dc:creator>
  <dc:creator>Oblet, C.</dc:creator>
  <dc:creator>Religa, A.</dc:creator>
  <dc:creator>Riquet, N.</dc:creator>
  <dc:creator>Mathieu, D.</dc:creator>
  <dc:creator>Yssel, H.</dc:creator>
  <dc:creator>/Veas, Francisco</dc:creator>
  <dc:subject>HIV</dc:subject>
  <dc:subject>gp120</dc:subject>
  <dc:subject>Tat Sf1</dc:subject>
  <dc:subject>SPT5</dc:subject>
  <dc:subject>HIV replication</dc:subject>
  <dc:subject>CXCR4</dc:subject>
  <dc:description>Objectives: The soluble HIV-1 gp120 envelope glycoprotein, after being shed from infected cells, can cross-link its receptors on both HIV-1 infected and non-infected target cells, leading to their activation. We have assessed the impact of soluble gp120 on viral replication in CD4+/CXCR4+ T cells, via its effects on Tat-mediated transactivation of the HIV-1/LTR. Materials and methods: Primary cord blood-derived CD4+/CXCR4+ T cells were stimulated with soluble recombinant gp120 (rgp120) from the HIV-1/HXB2 clone. The level of gene or protein expression was assessed by serial analysis gene expression (SAGE), reverse transcriptase-polymerase chain reaction, western blotting or flow-cytometry analysis. Cellular division of rgp120-stimulated T cells was assessed by CFDA-SE labeling. Long terminal repeat (LTR) activity and HIV infection level were respectively measured by a chemiluminescent P-gal Reporter Gene Assay and by p24 determination. Results: We have demonstrated that rgp120 activates both PKC epsilon and its upstream effector P13K/Akt, involved in the HIV-1 replication process. Moreover, rgp120 enhances the gene, as well as protein expression of the cellular Tat cofactors Tat-Sf1 and SPT5 in primary CD4+/CXCR4+ T cells. Finally, stimulation of HIV-1 infected T cells with rgp120 was found to result in both a higher LTR-activity and an increased production of viral particles. Conclusion: Taken together, these results show that soluble gp120 contributes to HIV-1 replication and dissemination, via the activation of multiple cell signaling pathways and the induction of Tat-cofactor expression, underscoring its potential as a therapeutic target in HIV-1-mediated pathogenesis. (c) 2005 Lippincott Williams and Wilkins.</dc:description>
  <dc:date>2005</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010042983</dc:identifier>
  <dc:identifier>fdi:010042983</dc:identifier>
  <dc:identifier>Miss&#xE9; Doroth&#xE9;e, Gajardo J., Oblet C., Religa A., Riquet N., Mathieu D., Yssel H., Veas Francisco. Soluble HIV-1 gp120 enhances HIV-1 replication in non-dividing CD4+T cells, mediated via cell signaling and Tat cofactor overexpression. 2005, 19 (9),  897-905</dc:identifier>
  <dc:language>EN</dc:language>
</oai_dc:dc>
