白细胞介素2受体
细胞生物学
效应器
FOXP3型
ZAP70型
白细胞介素21
生物
细胞凋亡
T细胞
细胞因子
蛋白激酶B
细胞毒性T细胞
TCIRG1公司
免疫系统
信号转导
免疫学
体外
生物化学
作者
Pushpa Pandiyan,Lixin Zheng,Satoru Ishihara,Jennifer L. Reed,Michael J. Lenardo
出处
期刊:Nature Immunology
[Springer Nature]
日期:2007-11-04
卷期号:8 (12): 1353-1362
被引量:1185
摘要
A key issue in mammalian immunology is how CD4+CD25+Foxp3+ regulatory T cells (T(reg) cells) suppress immune responses. Here we show that T(reg) cells induced apoptosis of effector CD4+ T cells in vitro and in vivo in a mouse model of inflammatory bowel disease. T(reg) cells did not affect the early activation or proliferation of effector CD4+ T cells. Cytokines that signal through the common gamma-chain suppressed T(reg) cell-induced apoptosis. T(reg) cell-induced effector CD4+ T cell death required the proapoptotic protein Bim, and effector CD4+ T cells incubated with T(reg) cells showed less activation of the prosurvival kinase Akt and less phosphorylation of the proapoptotic protein Bad. Thus, cytokine deprivation-induced apoptosis is a prominent mechanism by which T(reg) cells inhibit effector T cell responses.
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