Expression of insulin receptor mRNA and insulin receptor substrate 1 in pancreatic islet beta-cells

被引:95
作者
Harbeck, MC
Louie, DC
Howland, J
Wolf, BA
Rothenberg, PL
机构
[1] UNIV PENN, SCH MED, DEPT PATHOL & LAB MED, PHILADELPHIA, PA 19104 USA
[2] MEM SLOAN KETTERING CANC CTR, DEPT PATHOL, NEW YORK, NY USA
关键词
MESSENGER-RNA; GENE-EXPRESSION; FEEDBACK INHIBITION; B-CELLS; SECRETION; TISSUES; GROWTH; SEQUENCE; IDENTIFICATION; TRANSCRIPTION;
D O I
10.2337/diabetes.45.6.711
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The expression of insulin receptor mRNA was examined in rat pancreatic islet cells by single-cell reverse transcriptase (RT)-polymerase chain reaction (PCR), Single cells from disaggregated islets were individually isolated in a microcapillary pipet, and the beta-cells were identified by amplification of the mRNA for insulin, We found that in single beta-cells, the mRNA for the insulin receptor was also expressed, The fraction of single islet cells expressing both insulin receptor and insulin mRNAs corresponds closely to the fraction of beta-cells in the disaggregated islet cell preparation, These results indicate that normal beta-cells have the potential to express authentic insulin receptors, Immunohistochemical analysis was insufficiently sensitive for assaying insulin receptor protein; however, insulin receptor substrate 1 (IRS-1) was readily immuno-localized in islet beta-cells. Since IRS-1 links several cell surface receptors, including those for insulin and IGF-I, to distal signal transduction pathways, our observations indicate that hormonal regulation of islet beta-cells potentially involves the same signal transduction pathway that mediates insulin and growth factor signaling in peripheral insulin target tissue cell types.
引用
收藏
页码:711 / 717
页数:7
相关论文
共 56 条
[1]   IDENTIFICATION OF PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE IN PANCREATIC-ISLETS AND INSULIN-SECRETING BETA-CELLS [J].
ALTER, CA ;
WOLF, BA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (01) :190-197
[2]   PYRIDINE-NUCLEOTIDES IN PANCREATIC-ISLETS DURING INHIBITION OF INSULIN RELEASE BY EXOGENOUS INSULIN [J].
AMMON, HPT ;
VERSPOHL, E .
ENDOCRINOLOGY, 1976, 99 (06) :1468-1476
[3]   INSULIN SUPPRESSES ITS OWN SECRETION INVIVO [J].
ARGOUD, GM ;
SCHADE, DS ;
EATON, RP .
DIABETES, 1987, 36 (08) :959-962
[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]   TRANSCRIPTION OF THE DYSTROPHIN GENE IN HUMAN-MUSCLE AND NON-MUSCLE TISSUES [J].
CHELLY, J ;
KAPLAN, JC ;
MAIRE, P ;
GAUTRON, S ;
KAHN, A .
NATURE, 1988, 333 (6176) :858-860
[6]   ILLEGITIMATE TRANSCRIPTION - TRANSCRIPTION OF ANY GENE IN ANY CELL TYPE [J].
CHELLY, J ;
CONCORDET, JP ;
KAPLAN, JC ;
KAHN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (08) :2617-2621
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]   REGULATION OF INSULIN-SECRETION FROM BETA-CELL LINES DERIVED FROM TRANSGENIC MICE INSULINOMAS RESEMBLES THAT OF NORMAL BETA-CELLS [J].
DAMBRA, R ;
SURANA, M ;
EFRAT, S ;
STARR, RG ;
FLEISCHER, N .
ENDOCRINOLOGY, 1990, 126 (06) :2815-2822
[9]   FEEDBACK INHIBITION OF INSULIN ON INSULIN-SECRETION IN ISOLATED PANCREATIC-ISLETS [J].
DRAZNIN, B ;
GOODMAN, M ;
LEITNER, JW ;
SUSSMAN, KE .
ENDOCRINOLOGY, 1986, 118 (03) :1054-1058
[10]   ANALYSIS OF GENE-EXPRESSION IN SINGLE LIVE NEURONS [J].
EBERWINE, J ;
YEH, H ;
MIYASHIRO, K ;
CAO, YX ;
NAIR, S ;
FINNELL, R ;
ZETTEL, M ;
COLEMAN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :3010-3014