The effect of chronic exposure to fatty acids on gene expression in clonal insulin-producing cells: Studies using high density oligonucleotide microarray

被引:49
作者
Xiao, JZ
Gregersen, S
Kruhoffer, M
Pedersen, SB
Orntoft, TF
Hermansen, K
机构
[1] Aarhus Univ Hosp, Dept Endocrinol & Metab C, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Clin Biochem, Mol Diagnost Lab, DK-8200 Aarhus, Denmark
关键词
D O I
10.1210/en.142.11.4777
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fatty acids affect insulin secretion of pancreatic P-cells. Investigating gene expression profiles may help to characterize the underling mechanism. INS-1 cells were cultured with palmitate (0, 50, and 200 muM) for up to 44 d. Insulin secretion and expressions of 8740 genes were studied. We found that basal insulin secretion increased in cells exposed to palmitate. The response to glucose stimulation declined on d 44 in cells cultured at 200 mum palmitate. In response to 50 and 200 mum palmitate exposure, expression was changed in 11 and 99 genes on d 2 and 134 and in 159 genes on d 44, respectively. Genes involved in fatty acid oxidation were up-regulated, whereas those involved in glycolysis were down-regulated with 200 mum palmitate. A suppression of insulin receptor and insulin receptor substate-2 gene expression was found on d 44 in cells cultured at 200 mum palmitate. In conclusion, chronic exposure to low palmitate alters insulin secretion as well as gene expression. The number of genes that changed expression was palmitate dose and exposure time dependent. Randle's fatty acid-glucose cycle seems to be operative on the gene transcription level. A modification of expression of various genes may contribute to the functional changes.
引用
收藏
页码:4777 / 4784
页数:8
相关论文
共 53 条
[11]   Pharmacologic therapy for type 2 diabetes mellitus [J].
DeFronzo, RA .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (04) :281-303
[12]   Fatty acids decrease IDX-1 expression in rat pancreatic islets and reduce GLUT2, glucokinase, insulin, and somatostatin levels [J].
Gremlich, S ;
Bonny, C ;
Waeber, G ;
Thorens, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (48) :30261-30269
[13]  
Hashimoto T, 1996, J BIOCHEM-TOKYO, V119, P1196
[14]   Regulation of gene expression by dietary fat [J].
Jump, DB ;
Clarke, SD .
ANNUAL REVIEW OF NUTRITION, 1999, 19 :63-90
[15]   Tissue-specific insulin resistance in mice with mutations in the insulin receptor, IRS-1, and IRS-2 [J].
Kido, Y ;
Burks, DJ ;
Withers, D ;
Bruning, JC ;
Kahn, CR ;
White, MF ;
Accili, D .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (02) :199-205
[16]   Regulation of stearoyl-CoA desaturase genes: Role in cellular metabolism and preadipocyte differentiation [J].
Kim, YC ;
Ntambi, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 266 (01) :1-4
[17]   Tissue-specific knockout of the insulin receptor in pancreatic β cells creates an insulin secretory defect similar to that in type 2 diabetes [J].
Kulkarni, RN ;
Brüning, JC ;
Winnay, JN ;
Postic, C ;
Magnuson, MA ;
Kahn, CR .
CELL, 1999, 96 (03) :329-339
[18]   THE ROLE OF OMEGA-3-FATTY-ACIDS ON INSULIN-SECRETION AND INSULIN SENSITIVITY [J].
LARDINOIS, CK .
MEDICAL HYPOTHESES, 1987, 24 (03) :243-248
[19]   POLYUNSATURATED FATTY-ACIDS AUGMENT INSULIN-SECRETION [J].
LARDINOIS, CK ;
STARICH, GH ;
MAZZAFERRI, EL ;
DELETT, A .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1987, 6 (06) :507-515
[20]   Gene expression profile of aging and its retardation by caloric restriction [J].
Lee, CK ;
Klopp, RG ;
Weindruch, R ;
Prolla, TA .
SCIENCE, 1999, 285 (5432) :1390-1393