FOXP3型
效应器
白细胞介素2受体
流式细胞术
状态4
细胞因子
细胞生物学
转录因子
T细胞
抄写(语言学)
生物
免疫学
遗传学
基因
斯达
信号转导
免疫系统
哲学
车站3
语言学
作者
Daniela Fenoglio,Tiziana Altosole
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 35-47
被引量:1
标识
DOI:10.1007/978-1-0716-1311-5_3
摘要
The development of T helper (Th) cell subsets requires activated T cells that respond to a polarizing cytokine environment, resulting in the activation and expression of specific transcription factors. The subset-specific transcription factors are located either in the cytoplasm or in the nucleus, which determine the functional profile of Th populations, inducing the production of specific effector cytokines and functions. Flow cytometry analysis of transcription factors has become very common not only in research but also in immunologic follow-up protocols of patients recruited in clinical trials (as evaluation of CD4+CD25+ FOXP3+ T regulatory cells). Here, we propose and describe one-step protocols to evaluate the expression of transcription factors in mouse and human CD4+ lymphocytes, focusing the critical points of this cytometric approach.
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