Protein kinase Cβ (PKCβ):: Nomal functions and dieases

被引:59
作者
Kawakami, T [1 ]
Kawakami, Y [1 ]
Kitaura, J [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Allergy, San Diego, CA 92121 USA
关键词
BCR; diabetes; Fc epsilon RI; insulin; PKC beta;
D O I
10.1093/oxfordjournals.jbchem.a003273
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
PKCbetaI and PKCbetaII are DAG- and Ca2+-dependent conventional or classical isoforms of protein kinase C. Generated by alternative splicing from a single gene, they differ at their C-terminal 50 (betaI) or 52 (betaII) residues. They are expressed as major PKC isoforms in a variety of tissues, and thus the functions ascribed to "PKC" based on early studies using phorbol esters and PKC inhibitors could be attributed to them. As tools to probe into isoform-specific functions have recently become available, our understanding of the normal functions of these isoforms has dramatically increased. This minireview will focus mainly on two areas of signal transduction where the roles of PKCbetaI and PKCbetaII are relatively well-characterized: immunoreceptor and insulin receptor systems. Their involvement in disorders due to pertubations in these signaling systems, i.e., immunodeficiencies and diabetes, is also reviewed. Finally, patterns of PKC action in these and other biologic systems are discussed.
引用
收藏
页码:677 / 682
页数:6
相关论文
共 38 条
[21]   Protein kinase C: Structural and spatial regulation by phosphorylation, cofactors, and macromolecular interactions [J].
Newton, AC .
CHEMICAL REVIEWS, 2001, 101 (08) :2353-2364
[22]   Protein kinase C: a paradigm for regulation of protein function by two membrane-targeting modules [J].
Newton, AC ;
Johnson, JJ .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON BIOMEMBRANES, 1998, 1376 (02) :155-172
[23]   INTRACELLULAR SIGNALING BY HYDROLYSIS OF PHOSPHOLIPIDS AND ACTIVATION OF PROTEIN-KINASE-C [J].
NISHIZUKA, Y .
SCIENCE, 1992, 258 (5082) :607-614
[24]   EXPRESSION AND PROPERTIES OF 2 TYPES OF PROTEIN-KINASE-C - ALTERNATIVE SPLICING FROM A SINGLE GENE [J].
ONO, Y ;
KIKKAWA, U ;
OGITA, K ;
FUJII, T ;
KUROKAWA, T ;
ASAOKA, Y ;
SEKIGUCHI, K ;
ASE, K ;
IGARASHI, K ;
NISHIZUKA, Y .
SCIENCE, 1987, 236 (4805) :1116-1120
[25]  
OZAWA K, 1993, J BIOL CHEM, V268, P1749
[26]   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
[27]   PROTEIN-KINASES C-BETA AND C-EPSILON LINK THE MAST-CELL HIGH-AFFINITY RECEPTOR FOR IGE TO THE EXPRESSION OF C-FOS AND C-JUN [J].
RAZIN, E ;
SZALLASI, Z ;
KAZANIETZ, MG ;
BLUMBERG, PM ;
RIVERA, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7722-7726
[28]   Protein kinase C β controls nuclear factor κB activation in B cells through selective regulation of the IκB kinase α [J].
Saijo, K ;
Mecklenbräuker, I ;
Santana, A ;
Leitger, M ;
Schmedt, C ;
Tarakhovsky, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (12) :1647-1652
[29]   Protein kinase C-ζ and phosphoinositide-dependent protein kinase-1 are required for insulin-induced activation of ERK in rat adipocytes [J].
Sajan, MP ;
Standaert, ML ;
Bandyopadhyay, G ;
Quon, RJ ;
Burke, TR ;
Farese, RV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (43) :30495-30500
[30]   Adaptor proteins in protein kinase C-mediated signal transduction [J].
Schechtman, D ;
Mochly-Rosen, D .
ONCOGENE, 2001, 20 (44) :6339-6347