ABNORMAL REGULATION OF RIBOSOMAL-PROTEIN S6 KINASE BY INSULIN IN SKELETAL-MUSCLE OF INSULIN-RESISTANT HUMANS

被引:9
|
作者
SOMMERCORN, J
FIELDS, R
RAZ, I
MAEDA, R
机构
[1] Clinical Diabetes/Nutrition Section, National Institutes of Health, Phoenix, AZ 85016
来源
JOURNAL OF CLINICAL INVESTIGATION | 1993年 / 91卷 / 02期
关键词
NON-INSULIN-DEPENDENT DIABETES-MELLITUS; INSULIN RESISTANCE; INSULIN SIGNAL TRANSDUCTION; PROTEIN PHOSPHORYLATION; PROTEIN KINASE;
D O I
10.1172/JCI116229
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Insulin resistance in Pima Indians appears to result from a post-receptor impairment of insulin signal transduction that affects only some responses to insulin. To identify the primary lesion responsible for insulin resistance, we investigated the influence of insulin on ribosomal protein S6 kinase activities in skeletal muscle of insulin-sensitive and insulin-resistant nondiabetic Pima Indians during a 2-h hyperinsulinemic, euglycemic clamp. In sensitive subjects, S6 kinase activity was transiently activated fivefold over basal activity by 45 min of insulin infusion. Although basal activities in the two groups were similar, the response to insulin was delayed and restricted to about threefold over basal in subjects resistant to insulin. Two major S6 kinase activities in extracts of human muscle were resolved by chromatography on Mono Q. Peak 1, which accounted for basal activity owes to an enzyme antigenically related to the 90-kD S6 kinase II, a member of the rsk gene family. The major insulin-stimulated S6 kinase eluted as peak 2 and is antigenically related to a 70-kD S6 kinase. Our results show that insulin resistance impairs signaling to the 70-kD S6 kinase.
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页码:509 / 513
页数:5
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