Protein kinase c and AKT/protein kinase B in CD4+T-lymphocytes: new partners in TCR/CD28 signal integration

被引:36
作者
Bauer, B [1 ]
Baier, G [1 ]
机构
[1] Univ Innsbruck, Inst Med Biol & Human Genet, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
protein kinase C; AKT/protein kinase B; CD4+T-lymphocytes;
D O I
10.1016/S0161-5890(02)00011-1
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
T-cell biological responses appear to involve the complex interaction of T-cell surface receptors, intracellular signaling molecules and the cytoskeleton, Both the serine/threonine protein kinase families protein kinase C (PKC) and protein kinase B or RAC-PK (AKT/PKB) have been implicated in signal transmission leading to activation, differentiation as well as cellular survival of T-lymphocytes. The PKC gene family consists of nine diverse isotypes (PKCalpha, beta, gamma, delta, epsilon, xi, eta, theta and tau), the AKT/PKB gene family includes three kinases (AKT1/PKBalpha, AKT2/PKBbeta, AKT3/PKBgamma). Here. we attempt to summarize the regulation as well us downstream signaling pathways of PKC and AKT/PKB isotypes. that may act additive in TCR/CD28 induced proliferation and survival of peripheral CD4+ T-lymphocytes. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1087 / 1099
页数:13
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