Phosphorylation of IRS1 at serine 307 and serine 312 in response to insulin in human adipocytes

被引:12
作者
Danielsson, A
Nystrom, FH
Strålfors, P
机构
[1] Linkoping Univ, Dept Cell Biol, SE-58185 Linkoping, Sweden
[2] Linkoping Univ, Diabet Res Ctr, SE-58185 Linkoping, Sweden
关键词
insulin; insulin resistance; insulin receptor substrate-1; serine phosphorylation; tyrosine phosphorylation; positive feedback; negative feedback;
D O I
10.1016/j.bbrc.2006.02.075
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
Feedback control in insulin signaling involves serine phosphorylation of insulin receptor substrate-1 (IRS1). By analyzing the insulin-induced phosphorylation of IRS1 at serine 307, serine 312, and tyrosine in the same primary human adipocytes, we now report that negative feedback phosphorylation of serine 312 (corresponding to murine serine 307) required relatively high concentrations of insulin (EC50 = 3 nM) for a long time (t(1/2) ca. 30 min) and reduced the steady-state tyrosine phosphorylation, without affecting the cellular concentration, of IRS1. In contrast, positive feedback phosphorylation of serine 307 was a rapid (r(1/2) ca. 2 min) event at physiological concentrations of insulin (EC50 = 0.2 nM). (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1183 / 1187
页数:5
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