FOXP3型
流式细胞术
生物
白喉毒素
癌症研究
分子生物学
巨噬细胞
免疫印迹
免疫学
免疫系统
基因
微生物学
体外
遗传学
毒素
作者
Christel Devaud,Carmen S. Yong,Liza B. John,Jennifer A. Westwood,Connie P.M. Duong,Colin M. House,Delphine Denoyer,Jason Li,Phillip K. Darcy,Michael H. Kershaw
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2014-09-29
卷期号:9 (9): e108670-e108670
被引量:24
标识
DOI:10.1371/journal.pone.0108670
摘要
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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