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A more recent version of this article appeared on September 16, 2005
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M506000200v1
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Papers In Press, published online ahead of print June 8, 2005
J. Biol. Chem, 10.1074/jbc.M506000200
Submitted on June 2, 2005
Accepted on June 7, 2005

Palmitate inhibits insulin gene expression by altering PDX-1 nuclear localization and reducing MafA expression in isolated rat islets of langerhans

Derek K. Hagman, Lori B. Hays, Susan D. Parazzoli, and Vincent Poitout

Pacific Northwest Research Institute, Seattle, WA 98122

Corresponding Author: vpoitout{at}pnri.org

Abnormalities in lipid metabolism have been proposed as contributing factors to both defective insulin secretion from the pancreatic beta cell and peripheral insulin resistance in type 2 diabetes. Previously, we have shown that prolonged exposure of isolated rat islets of Langerhans to excessive fatty acid levels impairs insulin gene transcription. This study was designed to assess whether palmitate alters the expression and binding activity of the key regulatory factors pancreas-duodenum homeobox-1 (PDX-1), MafA, and Beta2, which respectively bind to the A3, C1, and E1 elements in the proximal region of the insulin promoter. Nuclear extracts of isolated rat islets cultured with 0.5 mM palmitate exhibited reduced binding activity to the A3 and C1 elements, but not the E1 element. Palmitate did not affect the overall expression of PDX-1, but reduced its nuclear localization. In contrast, palmitate blocked the stimulation of MafA mRNA and protein expression by glucose. Combined, adenovirus-mediated, over-expression of PDX-1 and MafA in islets completely prevented the inhibition of insulin gene expression by palmitate. These results demonstrate that prolonged exposure of islets to palmitate inhibits insulin gene transcription by impairing nuclear localization of PDX-1 and cellular expression of MafA.


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