Insulin Is Required to Maintain Albumin Expression by Inhibiting Forkhead Box O1 Protein.

J Biol Chem

From the Institute for Diabetes, Obesity, and Metabolism, Department of Biochemistry and Biophysics, and Graduate Group of Biochemistry and Molecular Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104 and the Cardiovascular and Metabolic Disease Research Unit, Pfizer Inc., Cambridge, Massachusetts 02140

Published: January 2016

Diabetes is accompanied by dysregulation of glucose, lipid, and protein metabolism. In recent years, much effort has been spent on understanding how insulin regulates glucose and lipid metabolism, whereas the effect of insulin on protein metabolism has received less attention. In diabetes, hepatic production of serum albumin decreases, and it has been long established that insulin positively controls albumin gene expression. In this study, we used a genetic approach in mice to identify the mechanism by which insulin regulates albumin gene transcription. Albumin expression was decreased significantly in livers with insulin signaling disrupted by ablation of the insulin receptor or Akt. Concomitant deletion of Forkhead Box O1 (Foxo1) in these livers rescued the decreased albumin secretion. Furthermore, activation of Foxo1 in the liver is sufficient to suppress albumin expression. These results suggest that Foxo1 acts as a repressor of albumin expression.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732219PMC
http://dx.doi.org/10.1074/jbc.M115.677351DOI Listing

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