Role of KLF15 in regulation of hepatic gluconeogenesis and metformin action

M Takashima, W Ogawa, K Hayashi, H Inoue… - Diabetes, 2010 - Am Diabetes Assoc
M Takashima, W Ogawa, K Hayashi, H Inoue, S Kinoshita, Y Okamoto, H Sakaue…
Diabetes, 2010Am Diabetes Assoc
OBJECTIVE An increase in the rate of gluconeogenesis is largely responsible for the
hyperglycemia in individuals with type 2 diabetes, with the antidiabetes action of metformin
being thought to be achieved at least in part through suppression of gluconeogenesis.
RESEARCH DESIGN AND METHODS We investigated whether the transcription factor
KLF15 has a role in the regulation of gluconeogenesis and whether KLF15 participates in
the antidiabetes effect of metformin. RESULTS Here we show that KLF15 regulates the …
OBJECTIVE
An increase in the rate of gluconeogenesis is largely responsible for the hyperglycemia in individuals with type 2 diabetes, with the antidiabetes action of metformin being thought to be achieved at least in part through suppression of gluconeogenesis.
RESEARCH DESIGN AND METHODS
We investigated whether the transcription factor KLF15 has a role in the regulation of gluconeogenesis and whether KLF15 participates in the antidiabetes effect of metformin.
RESULTS
Here we show that KLF15 regulates the expression of genes for gluconeogenic or amino acid–degrading enzymes in coordination with the transcriptional coactivator peroxisome proliferator–activated receptor γ coactivator 1α. Liver-specific ablation of KLF15 in diabetic mice resulted in downregulation of the expression of genes for gluconeogenic or amino acid catabolic enzymes and in amelioration of hyperglycemia. Exposure of cultured hepatocytes to metformin reduced the abundance of KLF15 through acceleration of its degradation and downregulation of its mRNA. Metformin suppressed the expression of genes for gluconeogenic or amino acid–degrading enzymes in cultured hepatocytes, and these effects of metformin were attenuated by restoration of KLF15 expression. Administration of metformin to mice inhibited both the expression of KLF15 and glucose production in the liver, the latter effect also being attenuated by restoration of hepatic KLF15 expression.
CONCLUSIONS
KLF15 plays an important role in regulation of the expression of genes for gluconeogenic and amino acid–degrading enzymes and that the inhibitory effect of metformin on gluconeogenesis is mediated at least in part by downregulation of KLF15 and consequent attenuation of the expression of such genes.
Am Diabetes Assoc