Protein-tyrosine phosphatase 1B substrates and metabolic regulation

被引:128
作者
Bakke, Jesse [1 ]
Haj, Fawaz G. [1 ,2 ,3 ]
机构
[1] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Internal Med, Div Endocrinol Diabet & Metab, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Ctr Comprehens Canc, Sacramento, CA 95817 USA
基金
美国国家卫生研究院;
关键词
PTP1B; Substrate; Obesity; Diabetes; ER stress; Pyruvate kinase; ENDOPLASMIC-RETICULUM STRESS; PYRUVATE-KINASE M2; INSULIN-RECEPTOR; BODY-WEIGHT; GLUCOSE-HOMEOSTASIS; SIGNAL-TRANSDUCTION; NEGATIVE REGULATION; MASS-SPECTROMETRY; REDOX REGULATION; S-NITROSYLATION;
D O I
10.1016/j.semcdb.2014.09.020
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Metabolic homeostasis requires integration of complex signaling networks which, when deregulated, contribute to metabolic syndrome and related disorders. Protein-tyrosine phosphatase 1B (PTP1B) has emerged as a key regulator of signaling networks that are implicated in metabolic diseases such as obesity and type 2 diabetes. In this review, we examine mechanisms that regulate PTP1B-substrate interaction, enzymatic activity and experimental approaches to identify PTP1B substrates. We then highlight findings that implicate PTP1B in metabolic regulation. In particular, insulin and leptin signaling are discussed as well as recently identified PTP1B substrates that are involved in endoplasmic reticulum stress response, cell-cell communication, energy balance and vesicle trafficking. In summary, PTP1B exhibits exquisite substrate specificity and is an outstanding pharmaceutical target for obesity and type 2 diabetes. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
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