INSULIN-INDUCED CIRCULAR MEMBRANE RUFFLING ON RAT-1 CELLS EXPRESSING A HIGH NUMBER OF HUMAN INSULIN-RECEPTORS - CIRCULAR RUFFLES CAUSED BY RAPID ACTIN REORGANIZATION EXHIBIT HIGH-DENSITY OF INSULIN-RECEPTORS AND PHOSPHOTYROSINES

被引:17
作者
LI, SL
MIYATA, Y
YAHARA, I
FUJITAYAMAGUCHI, Y
机构
[1] CITY HOPE NATL MED CTR,BECKMAN RES INT,DEPT MOLEC GENET,1450 E DUARTE RD,DUARTE,CA 91010
[2] TOKYO METROPOLITAN INST MED SCI,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
10.1006/excr.1993.1097
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The early effects of insulin on morphological changes were examined using Rat1 cells expressing ∼one million human insulin receptors (Rat1HIR cells). Insulin transiently induced circular membrane ruffling on Rat1HIR cells. The circular ruffles were detected by phase microscopy as well as by fluorescence microscopy when actin was stained with rhodamine-conjugated phalloidin. The circular ruffles were also visualized by fluorescence microscopy when stained with either anti-insulin receptor monoclonal antibody, αIR-1, or anti-phosphotyrosine antibody, followed by fluorescein isothiocyanate-labeled second antibodies. Control Rat1 cells or Rat1HIR A/K1018 cells expressing kinase-defective insulin receptors did not show any circular ruffles when treated with insulin. These results suggest that the circular ruffles are formed by actin reorganization induced by insulin and that this process requires the protein-tyrosine kinase activity of the receptor. Detection of insulin receptors and phosphotyrosines in the circular ruffles suggests the possibility that the insulin receptors in the ruffles may be highly active and phosphorylating either the receptors themselves or proteins associated with the ruffles. These results are consistent with our previous in vitro observations that a large aggregate form of the purified insulin receptor is a highly active protein-tyrosine kinase. © 1993 Academic Press, Inc.
引用
收藏
页码:353 / 360
页数:8
相关论文
共 31 条
[1]   TYROSINE PHOSPHORYLATION OF THE INSULIN-RECEPTOR IS NOT REQUIRED FOR RECEPTOR INTERNALIZATION - STUDIES IN 2,4-DINITROPHENOL-TREATED CELLS [J].
BACKER, JM ;
KAHN, CR ;
WHITE, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3209-3213
[2]   ACTIVATION OF THE HUMAN C-KIT PRODUCT BY LIGAND-INDUCED DIMERIZATION MEDIATES CIRCULAR ACTIN REORGANIZATION AND CHEMOTAXIS [J].
BLUMEJENSEN, P ;
CLAESSONWELSH, L ;
SIEGBAHN, A ;
ZSEBO, KM ;
WESTERMARK, B ;
HELDIN, CH .
EMBO JOURNAL, 1991, 10 (13) :4121-4128
[3]  
BUNK U, 1976, EXP CELL RES, V103, P295
[4]  
CHENKERS M, 1979, J CELL BIOL, V83, P260
[5]   COMPARISON OF RAPID CHANGES IN SURFACE-MORPHOLOGY AND COATED PIT FORMATION OF PC12 CELLS IN RESPONSE TO NERVE GROWTH-FACTOR, EPIDERMAL GROWTH-FACTOR, AND DIBUTYRYL-CYCLIC-AMP [J].
CONNOLLY, JL ;
GREEN, SA ;
GREENE, LA .
JOURNAL OF CELL BIOLOGY, 1984, 98 (02) :457-465
[6]   PDGF ALPHA-RECEPTORS AND BETA-RECEPTORS ACTIVATE UNIQUE AND COMMON SIGNAL TRANSDUCTION PATHWAYS [J].
ERIKSSON, A ;
SIEGBAHN, A ;
WESTERMARK, B ;
HELDIN, CH ;
CLAESSONWELSH, L .
EMBO JOURNAL, 1992, 11 (02) :543-550
[7]   RADIATION INACTIVATION EXPERIMENTS PREDICT THAT A LARGE AGGREGATE FORM OF THE INSULIN-RECEPTOR IS A HIGHLY-ACTIVE TYROSINE-SPECIFIC PROTEIN-KINASE [J].
FUJITAYAMAGUCHI, Y ;
HARMON, JT ;
KATHURIA, S .
BIOCHEMISTRY, 1989, 28 (11) :4556-4563
[8]   INSULIN-INDUCED FORMATION OF RUFFLING MEMBRANES OF KB CELLS AND ITS CORRELATION WITH ENHANCEMENT OF AMINO-ACID-TRANSPORT [J].
GOSHIMA, K ;
MASUDA, A ;
OWARIBE, K .
JOURNAL OF CELL BIOLOGY, 1984, 98 (03) :801-809
[9]  
KADOWAKI T, 1986, J BIOL CHEM, V261, P6141
[10]   DIRECT DEMONSTRATION THAT RECEPTOR CROSSLINKING OR AGGREGATION IS IMPORTANT IN INSULIN ACTION [J].
KAHN, CR ;
BAIRD, KL ;
JARRETT, DB ;
FLIER, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (09) :4209-4213