Protein Kinase B (PKB/Akt), a Key Mediator of the PI3K Signaling Pathway

被引:198
作者
Fayard, Elisabeth [1 ]
Xue, Gongda [1 ]
Parcellier, Arnaud [1 ]
Bozulic, Lana [1 ]
Hemmings, Brian A. [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
来源
PHOSPHOINOSITIDE 3-KINASE IN HEALTH AND DISEASE, VOL 1 | 2010年 / 346卷
关键词
PLECKSTRIN HOMOLOGY DOMAIN; T-CELL-RECEPTOR; AKT-DEPENDENT PHOSPHORYLATION; FORKHEAD TRANSCRIPTION FACTOR; ISOFORM-SPECIFIC REGULATION; SERINE-THREONINE KINASE; NITRIC-OXIDE SYNTHASE; RICTOR-MTOR COMPLEX; IN-VIVO; GLUCOSE-HOMEOSTASIS;
D O I
10.1007/82_2010_58
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 B (PKB/Akt) is a serine/threonine protein kinase that created serious interest when it was revealed as a mediator of the PI3K pathway. It comprises three isoforms that play both unique and redundant roles. Upon binding to phosphatidylinositol-(3,4,5)-trisphosphate (PIP3) generated by PI3K, PKB is phosphorylated by PDK1 at T308. To achieve full kinase activity, PKB needs to be phosphorylated at a second key residue, S473, by members of the PI3K-related kinase family mTORC2 or DNA-PK, depending on the stimulus and the context. Besides, a number of phosphatases and interacting partners have been shown to further modulate its subcellular localization, phosphorylation, and kinase activity. This review aims at illustrating the remarkable complexity in the regulation of PKB signaling downstream of PI3K. Such regulation could be attributed to the specific roles of the PKB isoforms, their expression pattern, subcellular localization, targets, phosphorylation by upstream kinases in a stimulus- and context-dependent manner and by phosphatases, and interaction with binding partners. This allows this key kinase to fulfill physiological functions in numerous processes, including embryonic development, thymocyte development, adipocyte differentiation, glucose homeostasis, and to avoid pathological loss of control such as tumor formation.
引用
收藏
页码:31 / 56
页数:26
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