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IFI16 knockdown in primary HIV-1 target cells

IFI16 is an important player of the host intrinsic immune response. Among others, it has been reported to sense intermediate products of HIV-1 reverse transcription in the cytosol and to sequester the transcription factor Sp1 in the nucleus to attenuate viral gene expression. Here, we present three...

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Detalles Bibliográficos
Autores principales: Bosso, Matteo, Bozzo, Caterina Prelli, Volcic, Meta, Kirchhoff, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753938/
https://www.ncbi.nlm.nih.gov/pubmed/33364624
http://dx.doi.org/10.1016/j.xpro.2020.100236
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author Bosso, Matteo
Bozzo, Caterina Prelli
Volcic, Meta
Kirchhoff, Frank
author_facet Bosso, Matteo
Bozzo, Caterina Prelli
Volcic, Meta
Kirchhoff, Frank
author_sort Bosso, Matteo
collection PubMed
description IFI16 is an important player of the host intrinsic immune response. Among others, it has been reported to sense intermediate products of HIV-1 reverse transcription in the cytosol and to sequester the transcription factor Sp1 in the nucleus to attenuate viral gene expression. Here, we present three different methods to reduce IFI16 protein expression levels in HIV-1 primary target cells. These techniques can be adapted for the investigation of other cellular factors in primary macrophages and CD4(+) T lymphocytes. For complete details on the use and execution of this protocol, please refer to Hotter et al. (2019) and Bosso et al. (2020).
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spelling pubmed-77539382020-12-23 IFI16 knockdown in primary HIV-1 target cells Bosso, Matteo Bozzo, Caterina Prelli Volcic, Meta Kirchhoff, Frank STAR Protoc Protocol IFI16 is an important player of the host intrinsic immune response. Among others, it has been reported to sense intermediate products of HIV-1 reverse transcription in the cytosol and to sequester the transcription factor Sp1 in the nucleus to attenuate viral gene expression. Here, we present three different methods to reduce IFI16 protein expression levels in HIV-1 primary target cells. These techniques can be adapted for the investigation of other cellular factors in primary macrophages and CD4(+) T lymphocytes. For complete details on the use and execution of this protocol, please refer to Hotter et al. (2019) and Bosso et al. (2020). Elsevier 2020-12-19 /pmc/articles/PMC7753938/ /pubmed/33364624 http://dx.doi.org/10.1016/j.xpro.2020.100236 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Bosso, Matteo
Bozzo, Caterina Prelli
Volcic, Meta
Kirchhoff, Frank
IFI16 knockdown in primary HIV-1 target cells
title IFI16 knockdown in primary HIV-1 target cells
title_full IFI16 knockdown in primary HIV-1 target cells
title_fullStr IFI16 knockdown in primary HIV-1 target cells
title_full_unstemmed IFI16 knockdown in primary HIV-1 target cells
title_short IFI16 knockdown in primary HIV-1 target cells
title_sort ifi16 knockdown in primary hiv-1 target cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753938/
https://www.ncbi.nlm.nih.gov/pubmed/33364624
http://dx.doi.org/10.1016/j.xpro.2020.100236
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