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Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice
Here, we describe an in vivo approach to visualize CD11c(+) cells in atherosclerosis. In particular, we use a protocol for X-Gal staining of immune cells within atherosclerotic plaques, which can be used as an alternative to analyze plaque composition and cell-specific molecules in atherogenesis. La...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420394/ https://www.ncbi.nlm.nih.gov/pubmed/36042879 http://dx.doi.org/10.1016/j.xpro.2022.101645 |
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author | Sauter, Manuela Sauter, Reinhard J. Olbrich, Marcus Thunemann, Martin Feil, Susanne Feil, Robert Langer, Harald F. |
author_facet | Sauter, Manuela Sauter, Reinhard J. Olbrich, Marcus Thunemann, Martin Feil, Susanne Feil, Robert Langer, Harald F. |
author_sort | Sauter, Manuela |
collection | PubMed |
description | Here, we describe an in vivo approach to visualize CD11c(+) cells in atherosclerosis. In particular, we use a protocol for X-Gal staining of immune cells within atherosclerotic plaques, which can be used as an alternative to analyze plaque composition and cell-specific molecules in atherogenesis. LacZ knockin mice have to be bred to mice carrying the CD11c(cre) recombinase—both brought onto an ApoE(−/−) background—to be able to visualize this cell type of interest in the plaques by X-Gal staining. With this approach, different immune cells in atherogenesis can be examined. For complete details on the use and execution of this protocol, please refer to Sauter et al. (2021). |
format | Online Article Text |
id | pubmed-9420394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94203942022-08-29 Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice Sauter, Manuela Sauter, Reinhard J. Olbrich, Marcus Thunemann, Martin Feil, Susanne Feil, Robert Langer, Harald F. STAR Protoc Protocol Here, we describe an in vivo approach to visualize CD11c(+) cells in atherosclerosis. In particular, we use a protocol for X-Gal staining of immune cells within atherosclerotic plaques, which can be used as an alternative to analyze plaque composition and cell-specific molecules in atherogenesis. LacZ knockin mice have to be bred to mice carrying the CD11c(cre) recombinase—both brought onto an ApoE(−/−) background—to be able to visualize this cell type of interest in the plaques by X-Gal staining. With this approach, different immune cells in atherogenesis can be examined. For complete details on the use and execution of this protocol, please refer to Sauter et al. (2021). Elsevier 2022-08-19 /pmc/articles/PMC9420394/ /pubmed/36042879 http://dx.doi.org/10.1016/j.xpro.2022.101645 Text en © 2022. https://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 Sauter, Manuela Sauter, Reinhard J. Olbrich, Marcus Thunemann, Martin Feil, Susanne Feil, Robert Langer, Harald F. Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title | Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title_full | Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title_fullStr | Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title_full_unstemmed | Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title_short | Protocol to visualize CD11c(+) cells in atherosclerosis using LacZ reporter mice |
title_sort | protocol to visualize cd11c(+) cells in atherosclerosis using lacz reporter mice |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420394/ https://www.ncbi.nlm.nih.gov/pubmed/36042879 http://dx.doi.org/10.1016/j.xpro.2022.101645 |
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