Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
38
pubmed:dateCreated
1998-10-15
pubmed:abstractText
Mutations in the hepatocyte nuclear factor-1alpha (HNF-1alpha) gene cause maturity onset diabetes of the young type 3, a form of type 2 diabetes mellitus. In mice lacking the HNF-1alpha gene, insulin secretion and intracellular calcium ([Ca2+]i) responses were impaired following stimulation with nutrient secretagogues such as glucose and glyceraldehyde but normal with non-nutrient stimuli such as potassium chloride. Patch clamp recordings revealed ATP-sensitive K+ currents (KATP) in beta-cells that were insensitive to suppression by glucose but normally sensitive to ATP. Exposure to mitochondrial substrates suppressed KATP, elevated [Ca2+]i, and corrected the insulin secretion defect. NAD(P)H responses to glucose were substantially reduced, and inhibitors of glycolytic NADH generation reproduced the mutant phenotype in normal islets. Flux of glucose through glycolysis in islets from mutant mice was reduced, as a result of which ATP generation in response to glucose was impaired. We conclude that hepatocyte nuclear factor-1alpha diabetes results from defective beta-cell glycolytic signaling, which is potentially correctable using substrates that bypass the defect.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Glyceraldehyde, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 1, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 1-alpha, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 1-beta, http://linkedlifedata.com/resource/pubmed/chemical/Hnf1a protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Hnf1b protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, http://linkedlifedata.com/resource/pubmed/chemical/Potassium Chloride, http://linkedlifedata.com/resource/pubmed/chemical/Tolbutamide, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
18
pubmed:volume
273
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
24457-64
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:9733737-Adenosine Triphosphate, pubmed-meshheading:9733737-Animals, pubmed-meshheading:9733737-Calcium, pubmed-meshheading:9733737-DNA-Binding Proteins, pubmed-meshheading:9733737-Glucose, pubmed-meshheading:9733737-Glyceraldehyde, pubmed-meshheading:9733737-Glycolysis, pubmed-meshheading:9733737-Hepatocyte Nuclear Factor 1, pubmed-meshheading:9733737-Hepatocyte Nuclear Factor 1-alpha, pubmed-meshheading:9733737-Hepatocyte Nuclear Factor 1-beta, pubmed-meshheading:9733737-Insulin, pubmed-meshheading:9733737-Islets of Langerhans, pubmed-meshheading:9733737-Membrane Potentials, pubmed-meshheading:9733737-Mice, pubmed-meshheading:9733737-Mice, Knockout, pubmed-meshheading:9733737-Nuclear Proteins, pubmed-meshheading:9733737-Patch-Clamp Techniques, pubmed-meshheading:9733737-Potassium Channels, pubmed-meshheading:9733737-Potassium Chloride, pubmed-meshheading:9733737-Signal Transduction, pubmed-meshheading:9733737-Tolbutamide, pubmed-meshheading:9733737-Transcription Factors
pubmed:year
1998
pubmed:articleTitle
Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice.
pubmed:affiliation
Department of Molecular Endocrinology, Glaxo Wellcome Research Institute, Research Triangle Park, North Carolina 27709, USA.
pubmed:publicationType
Journal Article, In Vitro, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't