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Inhibition of Small Maf Function in Pancreatic β-Cells Improves Glucose Tolerance Through the Enhancement of Insulin Gene Transcription and Insulin Secretion
- Publication Year :
- 2015
- Publisher :
- Endocrine Society, 2015.
-
Abstract
- The large-Maf transcription factor v-maf musculoaponeurotic fibrosarcoma oncogene homolog A (MafA) has been found to be crucial for insulin transcription and synthesis and for pancreatic beta-cell function and maturation. However, insights about the effects of small Maf factors on beta-cells are limited. Our goal was to elucidate the function of small-Maf factors on beta-cells using an animal model of endogenous small-Maf dysfunction. Transgenic (Tg) mice with beta-cell-specific expression of dominant-negative MafK (DN-MafK) experiments, which can suppress the function of all endogenous small-Mafs, were fed a high-fat diet, and their in vivo phenotypes were evaluated. Phenotypic analysis, glucose tolerance tests, morphologic examination of beta-cells, and islet experiments were performed. DN-MafK-expressed MIN6 cells were also used for in vitro analysis. The results showed that DN-MafK expression inhibited endogenous small-Maf binding to insulin promoter while increasing MafA binding. DN-MafK Tg mice under high-fat diet conditions showed improved glucose metabolism compared with control mice via incremental insulin secretion, without causing changes in insulin sensitivity or MafA expression. Moreover, up-regulation of insulin and glucokinase gene expression was observed both in vivo and in vitro under DN-MafK expression. We concluded that endogenous small-Maf factors negatively regulates beta-cell function by competing for MafA binding, and thus, the inhibition of small-Maf activity can improve beta-cell function.
- Subjects :
- Male
Transcriptional Activation
medicine.medical_specialty
Transcription, Genetic
medicine.medical_treatment
Endogeny
Mice, Transgenic
Biology
Carbohydrate metabolism
Diet, High-Fat
Islets of Langerhans
Mice
Endocrinology
Internal medicine
Insulin-Secreting Cells
Gene expression
medicine
Animals
Insulin
Transgenes
Promoter Regions, Genetic
Transcription factor
Original Research
Glucose tolerance test
medicine.diagnostic_test
Glucokinase
Glucose Tolerance Test
Immunohistochemistry
Mice, Inbred C57BL
Glucose
Phenotype
Proto-Oncogene Proteins c-maf
Biomarkers
Protein Binding
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....ba99d714a0223e7b17b087cea9544b07