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.
引用
收藏
页码:429 / 435
页数:7
相关论文
共 66 条
[31]   Protein kinase C-θ participates in NF-κB activation induced by CD3-CD28 costimulation through selective activation of IκB kinase β [J].
Lin, X ;
O'Mahony, A ;
Mu, YJ ;
Geleziunas, R ;
Greene, WC .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) :2933-2940
[32]   Bcl10 and MALT1, independent targets of chromosomal translocation in MALT lymphoma, cooperate in a novel NF-κB signaling pathway [J].
Lucas, PC ;
Yonezumi, M ;
Inohara, N ;
McAllister-Lucas, LM ;
Abazeed, ME ;
Chen, FF ;
Yamaoka, S ;
Seto, M ;
Núñez, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :19012-19019
[33]   Bimp1, a MAGUK family member linking protein kinase C activation to Bcl10-mediated NF-κB induction [J].
McAllister-Lucas, LM ;
Inohara, N ;
Lucas, PC ;
Ruland, J ;
Benito, A ;
Li, QT ;
Chen, S ;
Chen, FF ;
Yamaoka, S ;
Verma, IM ;
Mak, TW ;
Núñez, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (33) :30589-30597
[34]   Selective modulation of protein kinase C-theta during T-cell activation [J].
Monks, CRF ;
Kupfer, H ;
Tamir, I ;
Barlow, A ;
Kupfer, A .
NATURE, 1997, 385 (6611) :83-86
[35]   Mice lacking the CARD of CARMA1 exhibit defective B lymphocyte development and impaired proliferation of their B and T lymphocytes [J].
Newton, K ;
Dixit, VM .
CURRENT BIOLOGY, 2003, 13 (14) :1247-1251
[36]   The B lymphocyte adaptor molecule of 32 kD (Bam32) regulates B cell antigen receptor signaling and cell survival [J].
Niiro, H ;
Maeda, A ;
Kurosaki, T ;
Clark, EA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (01) :143-149
[37]   Regulation of B-cell fate by antigen-receptor signals [J].
Niiro, H ;
Clark, EA .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (12) :945-956
[38]   Bruton's tyrosine kinase is required for activation of IκB kinase and nuclear factor κB in response to B cell receptor engagement [J].
Petro, JB ;
Rahman, SMJ ;
Ballard, DW ;
Khan, WN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (10) :1745-1753
[39]   Phospholipase C-γ2 couples Bruton's tyrosine kinase to the NF-κB signaling pathway in B lymphocytes [J].
Petro, JB ;
Khan, WN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (03) :1715-1719
[40]   Impaired viability and profound block in thymocyte development in mice lacking the adaptor protein SLP-76 [J].
Pivniouk, V ;
Tsitsikov, E ;
Swinton, P ;
Rathbun, G ;
Alt, FW ;
Geha, RS .
CELL, 1998, 94 (02) :229-238