泛素连接酶
细胞生物学
T细胞
泛素
生物
化学
分子生物学
基因
免疫学
生物化学
免疫系统
作者
M. Safford,Samuel L. Collins,Michael A. Lutz,Amy N. Allen,Ching-Tai Huang,Jeanne Kowalski,Amanda L. Blackford,Maureen R. Horton,Charles G. Drake,Ronald H. Schwartz,Jonathan D. Powell
摘要
T cell receptor engagement in the absence of proper accessory signals leads to T cell anergy. E3 ligases are involved in maintaining the anergic state. However, the specific molecules responsible for the induction of anergy have yet to be elucidated. Using microarray analysis we have identified here early growth response gene 2 (Egr-2) and Egr-3 as key negative regulators of T cell activation. Overexpression of Egr2 and Egr3 was associated with an increase in the E3 ubiquitin ligase Cbl-b and inhibition of T cell activation. Conversely, T cells from Egr3(-/-) mice had lower expression of Cbl-b and were resistant to in vivo peptide-induced tolerance. These data support the idea that Egr-2 and Egr-3 are involved in promoting a T cell receptor-induced negative regulatory genetic program.
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