Evidence for an insulin receptor substrate 1 independent insulin signaling pathway that mediates insulin-responsive glucose transporter (GLUT4) translocation

被引:55
作者
Morris, AJ
Martin, SS
Haruta, T
Nelson, JG
Vollenweider, P
Gustafson, TA
Mueckler, M
Rose, DW
Olefsky, JM
机构
[1] UNIV CALIF SAN DIEGO,DEPT MED 0673,LA JOLLA,CA 92093
[2] UNIV MARYLAND,SCH MED,DEPT PHYSIOL,BALTIMORE,MD 21201
[3] WASHINGTON UNIV,SCH MED,DEPT CELL BIOL & PHYSIOL,ST LOUIS,MO 63110
[4] VET ADM MED CTR,RES SERV,SAN DIEGO,CA 92161
关键词
D O I
10.1073/pnas.93.16.8401
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interaction of the activated insulin receptor (IR) with its substrate, insulin receptor substrate 1 (IRS-1), via the phosphotyrosine binding domain of IRS-1 and the NPXY motif centered at phosphotyrosine 960 of the IR, is important for IRS-1 phosphorylation, We investigated the role of this interaction in the insulin signaling pathway that stimulates glucose transport, Utilizing microinjection of competitive inhibitory reagents in 3T3-L1 adipocytes, we have found that disruption of the IR/IRS-1 interaction has no effect upon translocation of the insulin-responsive glucose transporter (GLUT4). The activity of these reagents was demonstrated by their ability to block insulin stimulation of two distinct insulin bioeffects, membrane ruffling and mitogenesis, in 3T3-L1 adipocytes and insulin-responsive rat 1 fibroblasts, These data suggest that phosphorylated IRS-1 is not an essential component of the metabolic insulin signaling pathway that leads to GLUT4 translocation, yet it appears to be required for other insulin bioeffects.
引用
收藏
页码:8401 / 8406
页数:6
相关论文
共 32 条
[1]   HUMAN SKELETAL-MUSCLE INSULIN-RECEPTOR SUBSTRATE-1 - CHARACTERIZATION OF THE CDNA, GENE, AND CHROMOSOMAL LOCALIZATION [J].
ARAKI, E ;
SUN, XJ ;
HAAG, BL ;
CHUANG, LM ;
ZHANG, Y ;
YANGFENG, TL ;
WHITE, MF ;
KAHN, CR .
DIABETES, 1993, 42 (07) :1041-1054
[2]   CLONING OF THE MOUSE INSULIN-RECEPTOR SUBSTRATE-1 (IRS-1) GENE AND COMPLETE SEQUENCE OF MOUSE IRS-1 [J].
ARAKI, E ;
HAAG, BL ;
KAHN, CR .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1994, 1221 (03) :353-356
[3]   ALTERNATIVE PATHWAY OF INSULIN SIGNALING IN MICE WITH TARGETED DISRUPTION OF THE IRS-1 GENE [J].
ARAKI, E ;
LIPES, MA ;
PATTI, ME ;
BRUNING, JC ;
HAAG, B ;
JOHNSON, RS ;
KAHN, CR .
NATURE, 1994, 372 (6502) :186-190
[4]   PHOSPHATIDYLINOSITOL 3-KINASE ACTIVATION IS REQUIRED FOR INSULIN STIMULATION OF PP70 S6 KINASE, DNA-SYNTHESIS, AND GLUCOSE-TRANSPORTER TRANSLOCATION [J].
CHEATHAM, B ;
VLAHOS, CJ ;
CHEATHAM, L ;
WANG, L ;
BLENIS, J ;
KAHN, CR .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) :4902-4911
[5]   INSULIN ACTION AND THE INSULIN SIGNALING NETWORK [J].
CHEATHAM, B ;
KAHN, CR .
ENDOCRINE REVIEWS, 1995, 16 (02) :117-142
[6]   INHIBITION OF THE TRANSLOCATION OF GLUT1 AND GLUT4 IN 3T3-L1 CELLS BY THE PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR, WORTMANNIN [J].
CLARKE, JF ;
YOUNG, PW ;
YONEZAWA, K ;
KASUGA, M ;
HOLMAN, GD .
BIOCHEMICAL JOURNAL, 1994, 300 :631-635
[7]   NON-SH2 DOMAINS WITHIN INSULIN-RECEPTOR SUBSTRATE-1 AND SHC MEDIATE THEIR PHOSPHOTYROSINE-DEPENDENT INTERACTION WITH THE NPEY MOTIF OF THE INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR [J].
CRAPARO, A ;
ONEILL, TJ ;
GUSTAFSON, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (26) :15639-15643
[8]  
GUSTAFSON TA, 1995, MOL CELL BIOL, V15, P2500
[9]   INTRACELLULAR TARGETING OF THE INSULIN-REGULATABLE GLUCOSE TRANSPORTER (GLUT4) IS ISOFORM SPECIFIC AND INDEPENDENT OF CELL TYPE [J].
HANEY, PM ;
SLOT, JW ;
PIPER, RC ;
JAMES, DE ;
MUECKLER, M .
JOURNAL OF CELL BIOLOGY, 1991, 114 (04) :689-699
[10]   1-PHOSPHATIDYLINOSITOL 3-KINASE ACTIVITY IS REQUIRED FOR INSULIN-STIMULATED GLUCOSE-TRANSPORT BUT NOT FOR RAS ACTIVATION IN CHO CELLS [J].
HARA, K ;
YONEZAWA, K ;
SAKAUE, H ;
ANDO, A ;
KOTANI, K ;
KITAMURA, T ;
KITAMURA, Y ;
UEDA, H ;
STEPHENS, L ;
JACKSON, TR ;
HAWKINS, PT ;
DHAND, R ;
CLARK, AE ;
HOLMAN, GD ;
WATERFIELD, MD ;
KASUGA, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7415-7419