Metabolic, anabolic, and mitogenic insulin responses: A tissue-specific perspective for insulin receptor activators

被引:63
作者
Bedinger, Daniel H. [1 ]
Adams, Sean H. [2 ,3 ]
机构
[1] Xoma Corp, Berkeley, CA 94710 USA
[2] Arkansas Childrens Nutr Ctr, Little Rock, AR USA
[3] Univ Arkansas Med Sci, Dept Pediat, Little Rock, AR 72205 USA
基金
美国农业部;
关键词
Akt; ERK; Insulin; Insulin receptor; Diabetes; Insulin-like growth factor; GROWTH-FACTOR-I; PANCREATIC BETA-CELLS; PROTEIN-KINASE-C; SKELETAL-MUSCLE HYPERTROPHY; HEPATIC GLUCOSE-PRODUCTION; TYPE-2; DIABETES-MELLITUS; STAGE BREAST-CANCER; IGF-I; GENE-EXPRESSION; ADIPOSE-TISSUE;
D O I
10.1016/j.mce.2015.08.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Insulin acts as the major regulator of the fasting-to-fed metabolic transition by altering substrate metabolism, promoting energy storage, and helping activate protein synthesis. In addition to its glucoregulatory and other metabolic properties, insulin can also act as a growth factor. The metabolic and mitogenic responses to insulin are regulated by divergent post-receptor signaling mechanisms downstream from the activated insulin receptor (IR). However, the anabolic and growth-promoting properties of insulin require tissue-specific inter-relationships between the two pathways, and the nature and scope of insulin-regulated processes vary greatly across tissues. Understanding the nuances of this interplay between metabolic and growth-regulating properties of insulin would have important implications for development of novel insulin and IR modulator therapies that stimulate insulin receptor activation in both pathway- and tissue-specific manners. This review will provide a unique perspective focusing on the roles of "metabolic" and "mitogenic" actions of insulin signaling in various tissues, and how these networks should be considered when evaluating selective pharmacologic approaches to prevent or treat metabolic disease. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:143 / 156
页数:14
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