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Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice
The transcription factor Foxp3 represents the most specific functional marker of CD4(+) regulatory T cells (TRegs). However, previous reports have described Foxp3 expression in other cell types including some subsets of macrophages, although there are conflicting reports and Foxp3 expression in cell...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180934/ https://www.ncbi.nlm.nih.gov/pubmed/25264896 http://dx.doi.org/10.1371/journal.pone.0108670 |
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author | Devaud, Christel Yong, Carmen S. M. John, Liza B. Westwood, Jennifer A. Duong, Connie P. M. House, Colin M. Denoyer, Delphine Li, Jason Darcy, Phillip K. Kershaw, Michael H. |
author_facet | Devaud, Christel Yong, Carmen S. M. John, Liza B. Westwood, Jennifer A. Duong, Connie P. M. House, Colin M. Denoyer, Delphine Li, Jason Darcy, Phillip K. Kershaw, Michael H. |
author_sort | Devaud, Christel |
collection | PubMed |
description | The transcription factor Foxp3 represents the most specific functional marker of CD4(+) regulatory T cells (TRegs). However, previous reports have described Foxp3 expression in other cell types including some subsets of macrophages, although there are conflicting reports and Foxp3 expression in cells other than Treg is not well characterized. We performed detailed investigations into Foxp3 expression in macrophages in the normal tissue and tumor settings. We detected Foxp3 protein in macrophages infiltrating mouse renal cancer tumors injected subcutaneously or in the kidney. Expression was demonstrated using flow cytometry and Western blot with two individual monoclonal antibodies. Further analyses confirmed Foxp3 expression in macrophages by RT PCR, and studies using ribonucleic acid-sequencing (RNAseq) demonstrated a previously unknown Foxp3 messenger (m)RNA transcript in tumor-associated macrophages. In addition, depletion of Foxp3(+) cells using diphtheria toxin in Foxp3(DTR) mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. Collectively, these results indicate that tumor-associated macrophages could express Foxp3. |
format | Online Article Text |
id | pubmed-4180934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41809342014-10-07 Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice Devaud, Christel Yong, Carmen S. M. John, Liza B. Westwood, Jennifer A. Duong, Connie P. M. House, Colin M. Denoyer, Delphine Li, Jason Darcy, Phillip K. Kershaw, Michael H. PLoS One Research Article The transcription factor Foxp3 represents the most specific functional marker of CD4(+) regulatory T cells (TRegs). However, previous reports have described Foxp3 expression in other cell types including some subsets of macrophages, although there are conflicting reports and Foxp3 expression in cells other than Treg is not well characterized. We performed detailed investigations into Foxp3 expression in macrophages in the normal tissue and tumor settings. We detected Foxp3 protein in macrophages infiltrating mouse renal cancer tumors injected subcutaneously or in the kidney. Expression was demonstrated using flow cytometry and Western blot with two individual monoclonal antibodies. Further analyses confirmed Foxp3 expression in macrophages by RT PCR, and studies using ribonucleic acid-sequencing (RNAseq) demonstrated a previously unknown Foxp3 messenger (m)RNA transcript in tumor-associated macrophages. In addition, depletion of Foxp3(+) cells using diphtheria toxin in Foxp3(DTR) mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. Collectively, these results indicate that tumor-associated macrophages could express Foxp3. Public Library of Science 2014-09-29 /pmc/articles/PMC4180934/ /pubmed/25264896 http://dx.doi.org/10.1371/journal.pone.0108670 Text en © 2014 Devaud et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Devaud, Christel Yong, Carmen S. M. John, Liza B. Westwood, Jennifer A. Duong, Connie P. M. House, Colin M. Denoyer, Delphine Li, Jason Darcy, Phillip K. Kershaw, Michael H. Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title | Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title_full | Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title_fullStr | Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title_full_unstemmed | Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title_short | Foxp3 Expression in Macrophages Associated with RENCA Tumors in Mice |
title_sort | foxp3 expression in macrophages associated with renca tumors in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180934/ https://www.ncbi.nlm.nih.gov/pubmed/25264896 http://dx.doi.org/10.1371/journal.pone.0108670 |
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