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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 cells...
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Published in: | PloS one 2014-09, Vol.9 (9), p.e108670-e108670 |
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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 Foxp3DTR mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. Collectively, these results indicate that tumor-associated macrophages could express Foxp3. |
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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 Foxp3DTR mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. Collectively, these results indicate that tumor-associated macrophages could express Foxp3.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0108670</identifier><identifier>PMID: 25264896</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animals ; Antibodies, Monoclonal - immunology ; B cells ; Bioinformatics ; Biology and Life Sciences ; Cancer ; CD4 antigen ; Cell Line, Tumor ; Cloning ; Cytometry ; Diphtheria ; Diphtheria toxin ; Ethics ; Flow cytometry ; Forkhead Transcription Factors - biosynthesis ; Forkhead Transcription Factors - genetics ; Foxp3 protein ; Gene sequencing ; Immunoglobulins ; Immunology ; Immunoregulation ; Kidney cancer ; Kidney Neoplasms - immunology ; Kidneys ; Lymphocytes ; Lymphocytes T ; Macrophages ; Macrophages - immunology ; Mice ; Mice, Inbred BALB C ; Mice, SCID ; Monoclonal antibodies ; Oncology ; Ribonucleic acid ; RNA ; RNA, Messenger - biosynthesis ; T cells ; T-Lymphocytes, Regulatory - immunology ; Transcription factors ; Tumors</subject><ispartof>PloS one, 2014-09, Vol.9 (9), p.e108670-e108670</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Devaud et al. 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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 Foxp3DTR mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. 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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 Foxp3DTR mice reduced the frequency of type-2 macrophages (M2) in kidney tumors. Collectively, these results indicate that tumor-associated macrophages could express Foxp3.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25264896</pmid><doi>10.1371/journal.pone.0108670</doi><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Antibodies, Monoclonal - immunology B cells Bioinformatics Biology and Life Sciences Cancer CD4 antigen Cell Line, Tumor Cloning Cytometry Diphtheria Diphtheria toxin Ethics Flow cytometry Forkhead Transcription Factors - biosynthesis Forkhead Transcription Factors - genetics Foxp3 protein Gene sequencing Immunoglobulins Immunology Immunoregulation Kidney cancer Kidney Neoplasms - immunology Kidneys Lymphocytes Lymphocytes T Macrophages Macrophages - immunology Mice Mice, Inbred BALB C Mice, SCID Monoclonal antibodies Oncology Ribonucleic acid RNA RNA, Messenger - biosynthesis T cells T-Lymphocytes, Regulatory - immunology Transcription factors Tumors |
title | Foxp3 expression in macrophages associated with RENCA tumors in mice |
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