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
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