Protein kinase C and beyond

被引:239
作者
Spitaler, M [1 ]
Cantrell, DA [1 ]
机构
[1] Univ Dundee, Div Cell Biol & Immunol, Sch Life Sci, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
D O I
10.1038/ni1097
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Protein kinase C molecules regulate both positive and negative signal transduction pathways essential for the initiation and homeostasis of immune responses. There are multiple isoforms of protein kinase C that are activated differently by calcium and diacylglycerol, and these are activated mainly by antigen receptors in T cells, B cells and mast cells. Additionally, mammals express several other diacylglycerol binding proteins that are linked to a network of key signal transduction pathways that control lymphocyte biology. Diacylglycerol and protein kinase C regulate a broad range of gene transcription programs but also modulate integrins, chemokine responses and antigen receptors, thereby regulating lymphocyte adhesion, migration, differentiation and proliferation.
引用
收藏
页码:785 / 790
页数:6
相关论文
共 77 条
[1]   T cell activation and the cytoskeleton [J].
Acuto, O ;
Cantrell, D .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :165-+
[2]   Protein kinase C-θ (PKCθ):: it's all about location, location, location [J].
Altman, A ;
Villalba, M .
IMMUNOLOGICAL REVIEWS, 2003, 192 (01) :53-63
[3]   Protein kinase C-θ:: signaling from the center of the T-cell synapse [J].
Arendt, CW ;
Albrecht, B ;
Soos, TJ ;
Littman, DR .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (03) :323-330
[4]   Approaches to define antigen receptor-induced serine kinase signal transduction pathways [J].
Astoul, E ;
Laurence, AD ;
Totty, N ;
Beer, S ;
Alexander, DR ;
Cantrell, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (11) :9267-9275
[6]  
BAIER G, 1993, J BIOL CHEM, V268, P4997
[7]   PKCθ signals activation versus tolerance in vivo [J].
Berg-Brown, NN ;
Gronski, MA ;
Jones, RG ;
Elford, AK ;
Deenick, EK ;
Odermatt, B ;
Littman, DR ;
Ohashi, PS .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (06) :743-752
[8]  
BIRCHALL AM, 1994, J PHARMACOL EXP THER, V268, P922
[9]   INHIBITORS OF PROTEIN-KINASE-C .3. POTENT AND HIGHLY SELECTIVE BISINDOLYLMALEIMIDES BY CONFORMATIONAL RESTRICTION [J].
BIT, RA ;
DAVIS, PD ;
ELLIOTT, LH ;
HARRIS, W ;
HILL, CH ;
KEECH, E ;
KUMAR, H ;
LAWTON, G ;
MAW, A ;
NIXON, JS ;
VESEY, DR ;
WADSWORTH, J ;
WILKINSON, SE .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (01) :21-29
[10]   TCR comodulation of nonengaged TCR takes place by a protein kinase C and CD3γ di-leucine-based motif-dependent mechanism [J].
Bonefeld, CM ;
Rasmussen, AB ;
Lauritsen, JPH ;
von Essen, M ;
Odum, N ;
Andersen, PS ;
Geisler, C .
JOURNAL OF IMMUNOLOGY, 2003, 171 (06) :3003-3009