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Published online June 30, 2008
Diabetes 57:2708-2717, 2008
DOI: 10.2337/db07-1614
© 2008 by the American Diabetes Association
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miR-375 Targets 3'-Phosphoinositide–Dependent Protein Kinase-1 and Regulates Glucose-Induced Biological Responses in Pancreatic β-Cells

Abdelfattah El Ouaamari1,2, Nadine Baroukh1,2, Geert A. Martens3, Patricia Lebrun1,2, Daniel Pipeleers3, and Emmanuel van Obberghen1,2

1 Institut National de la Santé et de la Recherche Médicale, U907, Nice, France
2 Université de Nice-Sophia Antipolis, Faculté de Médecine, Institut de Génétique et Signalisation Moléculaire, IFR 50, Nice, France
3 Diabetes Research Center, Brussels Free University-VUB, Brussels, Belgium

Corresponding author: Emmanuel Van Obberghen, emmanuel.van-obberghen{at}unice.fr

OBJECTIVE—MicroRNAs are short, noncoding RNAs that regulate gene expression. We hypothesized that the phosphatidylinositol 3-kinase (PI 3-kinase) cascade known to be important in β-cell physiology could be regulated by microRNAs. Here, we focused on the pancreas-specific miR-375 as a potential regulator of its predicted target 3'-phosphoinositide–dependent protein kinase-1 (PDK1), and we analyzed its implication in the response of insulin-producing cells to elevation of glucose levels.

RESEARCH DESIGN AND METHODS—We used insulinoma-1E cells to analyze the effects of miR-375 on PDK1 protein level and downstream signaling using Western blotting, glucose-induced insulin gene expression using quantitative RT-PCR, and DNA synthesis by measuring thymidine incorporation. Moreover, we analyzed the effect of glucose on miR-375 expression in both INS-1E cells and primary rat islets. Finally, miR-375 expression in isolated islets was analyzed in diabetic Goto-Kakizaki (GK) rats.

RESULTS—We found that miR-375 directly targets PDK1 and reduces its protein level, resulting in decreased glucose-stimulatory action on insulin gene expression and DNA synthesis. Furthermore, glucose leads to a decrease in miR-375 precursor level and a concomitant increase in PDK1 protein. Importantly, regulation of miR-375 expression by glucose occurs in primary rat islets as well. Finally, miR-375 expression was found to be decreased in fed diabetic GK rat islets.

CONCLUSIONS—Our findings provide evidence for a role of a pancreatic-specific microRNA, miR-375, in the regulation of PDK1, a key molecule in PI 3-kinase signaling in pancreatic β-cells. The effects of glucose on miR-375 are compatible with the idea that miR-375 is involved in glucose regulation of insulin gene expression and β-cell growth.


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Related Article:

Role of MicroRNA in Pancreatic β-Cells: Where More Is Less
Michael D. Walker
Diabetes 2008 57: 2567-2568. [Extract] [Full Text] [PDF]



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M. D. Walker
Role of MicroRNA in Pancreatic {beta}-Cells: Where More Is Less
Diabetes, October 1, 2008; 57(10): 2567 - 2568.
[Full Text] [PDF]




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