Mouse Naive CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

被引:60
|
作者
Flaherty, Stephanie [1 ]
Reynolds, Joseph M. [1 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Dept Microbiol & Immunol, N Chicago, IL USA
来源
基金
美国国家卫生研究院;
关键词
Immunology; Issue; 98; Naive CD4(+) T cell; T helper cell; Th1; Th2; Th17; Treg; TRANSCRIPTION FACTOR GATA-3; PATHOGENIC T(H)17 CELLS; AUTOIMMUNE INFLAMMATION; TGF-BETA; LINEAGE; TH1; EXPRESSION; RESPONSES; DIRECTS; GENERATION;
D O I
10.3791/52739
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antigen inexperienced (naive) CD4(+) T cells undergo expansion and differentiation to effector subsets at the time of T cell receptor (TCR) recognition of cognate antigen presented on MHC class II. The cytokine signals present in the environment at the time of TCR activation are a major factor in determining the effector fate of a naive CD4(+) T cell. Although the cytokine environment during naive T cell activation may be complex and involve both redundant and opposing signals in vivo, the addition of various cytokine combinations during naive CD4(+) T cell activation in vitro can readily promote the establishment of effector T helper lineages with hallmark cytokine and transcription factor expression. Such differentiation experiments are commonly used as a first step for the evaluation of targets believed to promote or inhibit the development of certain CD4(+) T helper subsets. The addition of mediators, such as signaling agonists, antagonists, or other cytokines, during the differentiation process can also be used to study the influence of a particular target on T cell differentiation. Here, we describe a basic protocol for the isolation of naive T cells from mouse and the subsequent steps necessary for polarizing naive cells to various T helper effector lineages in vitro.
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页数:8
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