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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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). |
format | Online Article Text |
id | pubmed-7753938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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