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The roles of CARMA1, Bcl10, and MALT1 in antigen receptor signaling
被引:87
作者:
Lin, X
Wang, DM
机构:
[1] Univ Buffalo, Dept Microbiol & Immunol, Buffalo, NY 14214 USA
[2] Blood Ctr Southeastern Wisconsin, Blood Res Inst, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
关键词:
CARMAI;
BCl10;
MALTI/NF-kappa B;
antigen receptor signaling;
D O I:
10.1016/j.smim.2004.08.022
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Lymphocyte activation plays a critical role in immune responses. Dysregulation of lymphocyte activation can cause autoimmune, immunodeficient diseases, or leukemiaAymphoma. Lymphocyte activation is triggered by stimulation of antigen receptors, T cell receptors (TCR) or B cell receptors (BCR), on the surfaces of T or B lymphocyte, respectively. Stimulation of TCR or BCR induces a series of signal transduction cascades leading to activation of multiple transcription factors including NF-kappaB. Recent studies demonstrate that CARMA1, a scaffold protein, plays an essential role in mediating TCR- or BCR-induced NF-KB activation by recruiting two adaptor proteins, Bel 10 and MALT 1, to lipid rafts following stimulation of antigen receptors. In this review, we will discuss the mechanism by which proximal signaling components connect antigen receptor signaling to CARMA1, and how CARMA 1 regulates Bel 10 and MALT 1, leading to activation of NF-kappaB. In addition, the roles of CARMA1, Bcl10, and MALT 1 in lymphocyte activation and development will also be discussed. (C) 2004 Elsevier Ltd. All rights reserved.
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页码:429 / 435
页数:7
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