TRB3: A tribbles Homolog That Inhibits Akt/PKB Activation by Insulin in Liver
Joslin Diabetes Center · Salk Institute for Biological Studies · +1 more institution
Abstract
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…
Citation impact
- FWCI
- 9.50
- Percentile
- 100%
- References
- 24
Authors
4- KDKeyong DuCorresponding
Joslin Diabetes Center, Salk Institute for Biological Studies, Torrey Pines Institute For Molecular Studies
- SHStephan Herzig
Joslin Diabetes Center, Salk Institute for Biological Studies, Torrey Pines Institute For Molecular Studies
- RKRohit Kulkarni
Joslin Diabetes Center, Salk Institute for Biological Studies, Torrey Pines Institute For Molecular Studies
- MMMarc Montminy
Joslin Diabetes Center, Salk Institute for Biological Studies, Torrey Pines Institute For Molecular Studies
Topics & keywords
- Protein kinase B
- Insulin resistance
- Internal medicine
- Endocrinology
- Insulin
- Type 2 diabetes
- Insulin receptor
- Phosphorylation