Id1 expression promotes peripheral CD4+ T cell proliferation and survival upon TCR activation without co-stimulation

被引:6
作者
Liu, Chen [1 ]
Jin, Rong [1 ]
Wang, Hong-Cheng [2 ]
Tang, Hui [1 ]
Liu, Yuan-Feng [1 ]
Qian, Xiao-Ping [1 ]
Sun, Xiu-Yuan [1 ]
Ge, Qing [1 ]
Sun, Xiao-Hong [2 ]
Zhang, Yu [1 ]
机构
[1] Peking Univ, Dept Immunol, Hlth Sci Ctr, Beijing 100083, Peoples R China
[2] Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
基金
北京市自然科学基金;
关键词
Inhibitor of differentiation; E protein; CD4(+) T cell; Co-stimulation; T cell activation; LOOP-HELIX PROTEINS; NF-KAPPA-B; TRANSCRIPTION FACTORS; LYMPHOCYTE DEVELOPMENT; IMMUNE-SYSTEM; RECEPTOR; INTERLEUKIN-2; APOPTOSIS; SIGNAL; E2A;
D O I
10.1016/j.bbrc.2013.05.054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although the role of E proteins in the thymocyte development is well documented, much less is known about their function in peripheral T cells. Here we demonstrated that CD4 promoter-driven transgenic expression of Id1, a naturally occurring dominant-negative inhibitor of E proteins, can substitute for the co-stimulatory signal delivered by CD28 to facilitate the proliferation and survival of naive CD4(+) cells upon anti-CD3 stimulation. We next discovered that IL-2 production and NF-kappa B activity after anti-CD3 stimulation were significantly elevated in Id1-expressing cells, which may be, at least in part, responsible for the augmentation of their proliferation and survival. Taken together, results from this study suggest an important role of E and Id proteins in peripheral T cell activation. The ability of Id proteins to by-pass co-stimulatory signals to enable T cell activation has significant implications in regulating T cell immunity. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
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