ACTIVATION OF PHOSPHATIDYLINOSITOL-3-KINASE BY INSULIN IS MEDIATED BY BOTH A-HUMAN AND B-HUMAN INSULIN-RECEPTOR TYPES

被引:17
作者
CARRASCOSA, JM
VOGT, B
ULLRICH, A
HARING, HU
机构
[1] INST DIABETESFORSCHUNG,MUNICH,GERMANY
[2] MAX PLANCK INST BIOCHEM,W-8033 MARTINSRIED,GERMANY
关键词
D O I
10.1016/0006-291X(91)90494-R
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
Activation of a phosphatidylinositol-3-kinase (PI-3-kinase) is one of the earliest consequences of insulin binding to the receptor. The human insulin receptor exists in two isoforms which differ in the length of the α-subunit (HIR-A = 719 aa, HIR-B = 731 aa). To test whether both isoforms transduce an insulin signal on PI-3-kinase we used rat-1-fibroblasts expressing HIR-A or HIR-B. We found that insulin stimulates 32P incorporation into PIP through both HIR-A and HIR-B to a similar extent (approx. 8-10 fold). © 1991.
引用
收藏
页码:123 / 127
页数:5
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