Signalling through IGF-I and insulin receptors: where is the specificity?

被引:129
作者
Kim, JJ
Accili, D
机构
[1] Columbia Univ Coll Phys & Surg, Naomi Berrie Diabet Ctr, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
关键词
growth; metabolism; substrate phosphorylation; genetics; mouse models;
D O I
10.1054/ghir.2002.0265
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Receptor tyrosine kinases of the insulin-insulin-like growth factor (IGF) family promote growth and mediate metabolic signals. Despite their extensive structural homology, genetic evidence indicates that their physiological functions are distinct. Nevertheless, there is limited evidence from cell culture systems suggesting that their signalling capabilities differ. Thus, it remains unclear whether the different physiological roles of insulin and lGF-I receptors result from intrinsic differences in their abilities to activate distinct signalling pathways, or arise from extrinsic differences, such as tissue distribution, relative abundance and developmental regulation. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:84 / 90
页数:7
相关论文
共 61 条
[41]   Differential signaling of insulin and IGF-1 receptors to glycogen synthesis in murine hepatocytes [J].
Park, BC ;
Kido, Y ;
Accili, D .
BIOCHEMISTRY, 1999, 38 (23) :7517-7523
[42]   Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos [J].
Partanen, J ;
Schwartz, L ;
Rossant, J .
GENES & DEVELOPMENT, 1998, 12 (15) :2332-2344
[43]   Multiple signaling pathways of the insulin-like growth factor 1 receptor in protection from apoptosis [J].
Peruzzi, F ;
Prisco, M ;
Dews, M ;
Salomoni, P ;
Grassilli, E ;
Romano, G ;
Calabretta, B ;
Baserga, R .
MOLECULAR AND CELLULAR BIOLOGY, 1999, 19 (10) :7203-7215
[44]   Evidence that IRS-2 phosphorylation is required for insulin action in hepatocytes [J].
Rother, KI ;
Imai, Y ;
Caruso, M ;
Beguinot, F ;
Formisano, P ;
Accili, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17491-17497
[45]   Insulin receptor substrate-2 binds to the insulin receptor through its phosphotyrosine-binding domain and through a newly identified domain comprising amino acids 591-786 [J].
SawkaVerhelle, D ;
TartareDeckert, S ;
White, MF ;
vanObberghen, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :5980-5983
[46]   Cell Signaling by Receptor Tyrosine Kinases [J].
Lemmon, Mark A. ;
Schlessinger, Joseph .
CELL, 2010, 141 (07) :1117-1134
[47]   Increased IGFR activity and glucose transport in cultured skeletal muscle from insulin receptor null mice [J].
Shefi-Friedman, L ;
Wertheimer, E ;
Shen, S ;
Bak, A ;
Accili, D ;
Sampson, SR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 281 (01) :E16-E24
[48]   The differential effects of pp120 (Ceacam 1) on the mitogenic action of insulin and insulin-like growth factor 1 are regulated by the nonconserved tyrosine 1316 in the insulin receptor [J].
Soni, P ;
Lakkis, M ;
Poy, MN ;
Fernström, MA ;
Najjar, SM .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (11) :3896-3905
[49]   Liver regeneration .4. Transcriptional control of liver regeneration [J].
Taub, R .
FASEB JOURNAL, 1996, 10 (04) :413-427
[50]  
TORNQVIST HE, 1987, J BIOL CHEM, V262, P10212