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

被引:94
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
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