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How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission
Human immunodeficiency virus 1 (HIV-1) infects T cells, macrophages and dendritic cells and can manipulate their cytoskeleton structures at multiple steps during its replication cycle. Based on pharmacological and genetic targeting of cytoskeleton modulators, new imaging approaches and primary cell...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3187690/ https://www.ncbi.nlm.nih.gov/pubmed/21994805 http://dx.doi.org/10.3390/v3091757 |
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author | Lehmann, Martin Nikolic, Damjan S. Piguet, Vincent |
author_facet | Lehmann, Martin Nikolic, Damjan S. Piguet, Vincent |
author_sort | Lehmann, Martin |
collection | PubMed |
description | Human immunodeficiency virus 1 (HIV-1) infects T cells, macrophages and dendritic cells and can manipulate their cytoskeleton structures at multiple steps during its replication cycle. Based on pharmacological and genetic targeting of cytoskeleton modulators, new imaging approaches and primary cell culture models, important roles for actin and microtubules during entry and cell-to-cell transfer have been established. Virological synapses and actin-containing membrane extensions can mediate HIV-1 transfer from dendritic cells or macrophage cells to T cells and between T cells. We will review the role of the cytoskeleton in HIV-1 entry, cellular trafficking and cell-to-cell transfer between primary cells. |
format | Online Article Text |
id | pubmed-3187690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-31876902011-10-12 How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission Lehmann, Martin Nikolic, Damjan S. Piguet, Vincent Viruses Review Human immunodeficiency virus 1 (HIV-1) infects T cells, macrophages and dendritic cells and can manipulate their cytoskeleton structures at multiple steps during its replication cycle. Based on pharmacological and genetic targeting of cytoskeleton modulators, new imaging approaches and primary cell culture models, important roles for actin and microtubules during entry and cell-to-cell transfer have been established. Virological synapses and actin-containing membrane extensions can mediate HIV-1 transfer from dendritic cells or macrophage cells to T cells and between T cells. We will review the role of the cytoskeleton in HIV-1 entry, cellular trafficking and cell-to-cell transfer between primary cells. Molecular Diversity Preservation International (MDPI) 2011-09-15 /pmc/articles/PMC3187690/ /pubmed/21994805 http://dx.doi.org/10.3390/v3091757 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Lehmann, Martin Nikolic, Damjan S. Piguet, Vincent How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title | How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title_full | How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title_fullStr | How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title_full_unstemmed | How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title_short | How HIV-1 Takes Advantage of the Cytoskeleton during Replication and Cell-to-Cell Transmission |
title_sort | how hiv-1 takes advantage of the cytoskeleton during replication and cell-to-cell transmission |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3187690/ https://www.ncbi.nlm.nih.gov/pubmed/21994805 http://dx.doi.org/10.3390/v3091757 |
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