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.
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页码:4777 / 4784
页数:8
相关论文
共 53 条
[31]  
2-C
[32]  
REAVEN GM, 1991, AM J MED S2A, V90, P7
[33]   Insulin secretion: Feed-forward control of insulin biosynthesis? [J].
Rutter, GA .
CURRENT BIOLOGY, 1999, 9 (12) :R443-R445
[34]   Identification of fatty acid methyl ester as naturally occurring transcriptional regulators of the members of the peroxisome proliferator-activated receptor family [J].
Schmidt, A ;
Vogel, RL ;
Witherup, KM ;
Rutledge, SJ ;
Pitzenberger, SM ;
Adam, M ;
Rodan, GA .
LIPIDS, 1996, 31 (11) :1115-1124
[35]   Quantitative reverse transcription-polymerase chain reaction to study mRNA decay: Comparison of endpoint and real-time methods [J].
Schmittgen, TD ;
Zakrajsek, BA ;
Mills, AG ;
Gorn, V ;
Singer, MJ ;
Reed, MW .
ANALYTICAL BIOCHEMISTRY, 2000, 285 (02) :194-204
[36]   Lipid rather than glucose metabolism is implicated in altered insulin secretion caused by oleate in INS-1 cells [J].
Segall, L ;
Lameloise, N ;
Assimacopoulos-Jeannet, F ;
Roche, E ;
Corkey, P ;
Thumelin, S ;
Corkey, BE ;
Prentki, M .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (03) :E521-E528
[37]   Differential expression of the insulin gene transcriptional repressor CCAAT/enhancer-binding protein β and transactivator islet duodenum homeobox-1 in rat pancreatic β cells during the development of diabetes mellitus [J].
Seufert, J ;
Weir, GC ;
Habener, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (11) :2528-2539
[38]  
Shafrir E, 1996, DIABETES METAB, V22, P122
[39]   Study of genetic prediabetic South Indian subjects -: Importance of hyperinsulinemia and β-cell dysfunction [J].
Snehalatha, C ;
Ramachandran, A ;
Satyavani, K ;
Latha, E ;
Viswanathan, V .
DIABETES CARE, 1998, 21 (01) :76-79
[40]   Effects of troglitazone on substrate storage and utilization in insulin-resistant rats [J].
Sreenan, S ;
Keck, S ;
Fuller, T ;
Cockburn, B ;
Burant, CF .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 276 (06) :E1119-E1129