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Scientific article
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Mitochondrial dysfunction contributes to impaired insulin secretion in INS-1 cells with dominant-negative mutations of HNF-1alpha and in HNF-1alpha-deficient islets

Published inThe Journal of biological chemistry, vol. 284, no. 25, p. 16808-16821
Publication date2009
Abstract

Maturity Onset Diabetes of the Young-type 3 (MODY-3) has been linked to mutations in the transcription factor hepatic nuclear factor (HNF)-1alpha, resulting in deficiency in glucose-stimulated insulin secretion. In INS-1 cells overexpressing doxycycline-inducible HNF-1alpha dominant-negative (DN-) gene mutations, and islets from Hnf-1alpha knock-out mice, insulin secretion was impaired in response to glucose (15 mm) and other nutrient secretagogues. Decreased rates of insulin secretion in response to glutamine plus leucine and to methyl pyruvate, but not potassium depolarization, indicate defects specific to mitochondrial metabolism. To identify the biochemical mechanisms responsible for impaired insulin secretion, we used (31)P NMR measured mitochondrial ATP synthesis (distinct from glycolytic ATP synthesis) together with oxygen consumption measurements to determine the efficiency of mitochondrial oxidative phosphorylation. Mitochondrial uncoupling was significantly higher in DN-HNF-1alpha cells, such that rates of ATP synthesis were decreased by approximately one-half in response to the secretagogues glucose, glutamine plus leucine, or pyruvate. In addition to closure of the ATP-sensitive K(+) channels with mitochondrial ATP synthesis, mitochondrial production of second messengers through increased anaplerotic flux has been shown to be critical for coupling metabolism to insulin secretion. (13)C-Isotopomer analysis and tandem mass spectrometry measurement of Krebs cycle intermediates revealed a negative impact of DN-HNF-1alpha and Hnf-1alpha knock-out on mitochondrial second messenger production with glucose but not amino acids. Taken together, these results indicate that, in addition to reduced glycolytic flux, uncoupling of mitochondrial oxidative phosphorylation contributes to impaired nutrient-stimulated insulin secretion with either mutations or loss of HNF-1alpha.

Keywords
  • Adenosine Triphosphate/biosynthesis
  • Animals
  • Base Sequence
  • Cell Line
  • DNA Primers/genetics
  • Diabetes Mellitus, Type 2/genetics/physiopathology
  • Female
  • Glucose/pharmacology
  • Glucose Transporter Type 2/genetics
  • Glutamine/pharmacology
  • Glycolysis
  • Hepatocyte Nuclear Factor 1-alpha/deficiency/genetics/metabolism
  • Humans
  • Insulin/secretion
  • Islets of Langerhans/drug effects/metabolism/secretion
  • Leucine/pharmacology
  • Male
  • Mice
  • Mice, Knockout
  • Mitochondria/drug effects/metabolism
  • Mutation
  • Oxidative Phosphorylation
  • Pyruvic Acid/pharmacology
  • RNA, Messenger/genetics/metabolism
  • Rats
Citation (ISO format)
PONGRATZ, Rebecca L. et al. Mitochondrial dysfunction contributes to impaired insulin secretion in INS-1 cells with dominant-negative mutations of HNF-1alpha and in HNF-1alpha-deficient islets. In: The Journal of biological chemistry, 2009, vol. 284, n° 25, p. 16808–16821. doi: 10.1074/jbc.M807723200
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Article (Published version)
accessLevelRestricted
Identifiers
ISSN of the journal0021-9258
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