Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5625
pubmed:dateCreated
2003-6-6
pubmed:abstractText
Insulin resistance is a major hallmark in the development of type II diabetes, which is characterized by the failure of insulin to promote glucose uptake in muscle and to suppress glucose production in liver. The serine-threonine kinase Akt (PKB) is a principal target of insulin signaling that inhibits hepatic glucose output when glucose is available from food. Here we show that TRB3, a mammalian homolog of Drosophila tribbles, functions as a negative modulator of Akt. TRB3 expression is induced in liver under fasting conditions, and TRB3 disrupts insulin signaling by binding directly to Akt and blocking activation of the kinase. Amounts of TRB3 RNA and protein were increased in livers of db/db diabetic mice compared with those in wild-type mice. Hepatic overexpression of TRB3 in amounts comparable to those in db/db mice promoted hyperglycemia and glucose intolerance. Our results suggest that, by interfering with Akt activation, TRB3 contributes to insulin resistance in individuals with susceptibility to type II diabetes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/AKT1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Akt1 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Glycogen Synthase Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1095-9203
pubmed:author
pubmed:issnType
Electronic
pubmed:day
6
pubmed:volume
300
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1574-7
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12791994-Adenoviridae, pubmed-meshheading:12791994-Amino Acid Substitution, pubmed-meshheading:12791994-Animals, pubmed-meshheading:12791994-Blood Glucose, pubmed-meshheading:12791994-Cell Cycle Proteins, pubmed-meshheading:12791994-Cell Line, pubmed-meshheading:12791994-Diabetes Mellitus, pubmed-meshheading:12791994-Enzyme Activation, pubmed-meshheading:12791994-Fasting, pubmed-meshheading:12791994-Genetic Vectors, pubmed-meshheading:12791994-Glucose, pubmed-meshheading:12791994-Glucose Intolerance, pubmed-meshheading:12791994-Glycogen Synthase Kinase 3, pubmed-meshheading:12791994-Humans, pubmed-meshheading:12791994-Insulin, pubmed-meshheading:12791994-Insulin Resistance, pubmed-meshheading:12791994-Insulin-Like Growth Factor I, pubmed-meshheading:12791994-Liver, pubmed-meshheading:12791994-Male, pubmed-meshheading:12791994-Mice, pubmed-meshheading:12791994-Mice, Inbred C57BL, pubmed-meshheading:12791994-Phosphorylation, pubmed-meshheading:12791994-Polymerase Chain Reaction, pubmed-meshheading:12791994-Protein-Serine-Threonine Kinases, pubmed-meshheading:12791994-Proto-Oncogene Proteins, pubmed-meshheading:12791994-Proto-Oncogene Proteins c-akt, pubmed-meshheading:12791994-RNA Interference, pubmed-meshheading:12791994-Rats, pubmed-meshheading:12791994-Repressor Proteins, pubmed-meshheading:12791994-Signal Transduction, pubmed-meshheading:12791994-Transfection, pubmed-meshheading:12791994-Transgenes, pubmed-meshheading:12791994-Tumor Cells, Cultured, pubmed-meshheading:12791994-Two-Hybrid System Techniques
pubmed:year
2003
pubmed:articleTitle
TRB3: a tribbles homolog that inhibits Akt/PKB activation by insulin in liver.
pubmed:affiliation
Peptide Biology Laboratories, Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037-1002, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't