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      Identification of Vimentin as a Potential Therapeutic Target against HIV Infection

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          Abstract

          A combination of antiviral drugs known as antiretroviral therapy (ART) has shown effectiveness against the human immunodeficiency virus (HIV). ART has markedly decreased mortality and morbidity among HIV-infected patients, having even reduced HIV transmission. However, an important current disadvantage, resistance development, remains to be solved. Hope is focused on developing drugs against cellular targets. This strategy is expected to prevent the emergence of viral resistance. In this study, using a comparative proteomic approach in MT4 cells treated with an anti-HIV leukocyte extract, we identified vimentin, a molecule forming intermediate filaments in the cell, as a possible target against HIV infection. We demonstrated a strong reduction of an HIV-1 based lentivirus expressing the enhanced green fluorescent protein (eGFP) in vimentin knockdown cells, and a noteworthy decrease of HIV-1 capsid protein antigen (CAp24) in those cells using a multiround infectivity assay. Electron micrographs showed changes in the structure of intermediate filaments when MT4 cells were treated with an anti-HIV leukocyte extract. Changes in the structure of intermediate filaments were also observed in vimentin knockdown MT4 cells. A synthetic peptide derived from a cytoskeleton protein showed potent inhibitory activity on HIV-1 infection, and low cytotoxicity. Our data suggest that vimentin can be a suitable target to inhibit HIV-1.

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          Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity.

          Maraviroc (UK-427,857) is a selective CCR5 antagonist with potent anti-human immunodeficiency virus type 1 (HIV-1) activity and favorable pharmacological properties. Maraviroc is the product of a medicinal chemistry effort initiated following identification of an imidazopyridine CCR5 ligand from a high-throughput screen of the Pfizer compound file. Maraviroc demonstrated potent antiviral activity against all CCR5-tropic HIV-1 viruses tested, including 43 primary isolates from various clades and diverse geographic origin (geometric mean 90% inhibitory concentration of 2.0 nM). Maraviroc was active against 200 clinically derived HIV-1 envelope-recombinant pseudoviruses, 100 of which were derived from viruses resistant to existing drug classes. There was little difference in the sensitivity of the 200 viruses to maraviroc, as illustrated by the biological cutoff in this assay (= geometric mean plus two standard deviations [SD] of 1.7-fold). The mechanism of action of maraviroc was established using cell-based assays, where it blocked binding of viral envelope, gp120, to CCR5 to prevent the membrane fusion events necessary for viral entry. Maraviroc did not affect CCR5 cell surface levels or associated intracellular signaling, confirming it as a functional antagonist of CCR5. Maraviroc has no detectable in vitro cytotoxicity and is highly selective for CCR5, as confirmed against a wide range of receptors and enzymes, including the hERG ion channel (50% inhibitory concentration, >10 microM), indicating potential for an excellent clinical safety profile. Studies in preclinical in vitro and in vivo models predicted maraviroc to have human pharmacokinetics consistent with once- or twice-daily dosing following oral administration. Clinical trials are ongoing to further investigate the potential of using maraviroc for the treatment of HIV-1 infection and AIDS.
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            Global report: UNAIDS report on the global AIDS epidemic 2012

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              The function of intermediate filaments in cell shape and cytoskeletal integrity

              This study describes the development and use of a specific method for disassembling intermediate filament (IF) networks in living cells. It takes advantage of the disruptive effects of mimetic peptides derived from the amino acid sequence of the helix initiation 1A domain of IF protein chains. The results demonstrate that at 1:1 molar ratios, these peptides disassemble vimentin IF into small oligomeric complexes and monomers within 30 min at room temperature in vitro. Upon microinjection into cultured fibroblasts, these same peptides induce the rapid disassembly of IF networks. The disassembly process is accompanied by a dramatic alteration in cell shape and the destabilization of microtubule and actin-stress fiber networks. These changes in cell shape and IF assembly states are reversible. The results are discussed with respect to the roles of IF in cell shape and the maintenance of the integrity and mechanical properties of the cytoplasm, as well as the stability of the other major cytoskeletal systems.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Viruses
                Viruses
                viruses
                Viruses
                MDPI
                1999-4915
                15 June 2016
                June 2016
                : 8
                : 6
                : 98
                Affiliations
                [1 ]Center for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba; anna.ramirez@ 123456cigb.edu.cu (A.R.); dionne.casillas@ 123456cigb.edu.cu (D.C.); taimi.paneque@ 123456cigb.edu.cu (T.P.); raimundo.ubieta@ 123456cigb.edu.cu (R.U.); lilacastellanos@ 123456infomed.sld.cu (L.C.-S.); carlos.duarte@ 123456cigb.edu.cu (C.D.); viviana.falcon@ 123456cigb.edu.cu (V.F.); osvaldo.reyes@ 123456cigb.edu.cu (O.R.); hilda.garay@ 123456cigb.edu.cu (H.G.); yassel.ramos@ 123456cigb.edu.cu (Y.R.); vladimir.besada@ 123456cigb.edu.cu (V.B.); lazaro.betancourt@ 123456cigb.edu.cu (L.B.)
                [2 ]Laboratory for AIDS Research, Carretera de Tapaste y Autopista Nacional, San José de las Lajas, Mayabeque CP 32700, Cuba; cicdc@ 123456infomed.sld.cu (M.D.); riverora@ 123456infomed.sld.cu (L.N.); eladio.silva@ 123456infomed.sld.cu (E.S.); enrnoa@ 123456infomed.sld.cu (E.N.)
                Author notes
                [* ]Correspondence: celia.fernandez@ 123456cigb.edu.cu ; Tel.: +53-7-250-4396; Fax: +53-7-250-4494
                Article
                viruses-08-00098
                10.3390/v8060098
                4926169
                27314381
                1e51d64e-f685-4c5b-9938-3c3b4feb5fd1
                © 2016 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 01 October 2015
                : 06 April 2016
                Categories
                Article

                Microbiology & Virology
                leukocyte extract,vimentin,intermediate filaments,cytoskeleton,hiv,anti-hiv activity,proteomics

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