Pdx-1 enables insulin secretion by regulating synaptotagmin 1 gene expression

Biochem Biophys Res Commun. 2004 Jun 4;318(3):631-5. doi: 10.1016/j.bbrc.2004.04.071.

Abstract

Pdx-1 plays important roles both in the development of the pancreas and in maintaining pancreatic beta cell function. However, the role of Pdx-1 in the regulation of insulin release is not well established. We previously demonstrated that Pdx-1 overcomes the defect in insulin release from the insulin-producing cells derived from small hepatocytes (SHCs). Insulin secretion is regulated in vivo by the sequential events triggered by the increase of intracellular Ca(2+)-concentration in response to high glucose concentration. In the present study, we identified a new target of Pdx-1 involved in insulin release. Pdx-1 positively regulates the transcription of the gene encoding synaptotagmin 1 (Syt1) (a Ca(2+)-sensor that plays a central role in insulin release) through Pdx-1-binding sites within the 3' regulatory region of the Syt1 gene. We further demonstrated the essential role of Pdx-1 in insulin secretion by the gene knock-down strategy. Small interfering RNA (siRNA) directed against Pdx-1 specifically reduced the levels of Pdx-1 protein and Syt1 transcript in insulinoma lines. Our data indicate that Pdx-1 might contribute to the regulation of insulin release by promoting Syt1 expression in vivo, and provide useful information for future therapy of diabetes mellitus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Calcium-Binding Proteins*
  • Gene Expression Regulation / physiology
  • Genes, Reporter
  • Genetic Vectors
  • Hepatocytes / cytology
  • Hepatocytes / metabolism
  • Homeodomain Proteins*
  • Immunoblotting
  • Insulin / metabolism*
  • Insulin Secretion
  • Islets of Langerhans / metabolism
  • Luciferases / metabolism
  • Membrane Glycoproteins / biosynthesis*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • RNA Interference
  • Rats
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Synaptotagmin I
  • Synaptotagmins
  • Trans-Activators / physiology*
  • Transcription, Genetic
  • Transfection

Substances

  • Calcium-Binding Proteins
  • Homeodomain Proteins
  • Insulin
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • Recombinant Proteins
  • Synaptotagmin I
  • Syt1 protein, mouse
  • Syt1 protein, rat
  • Trans-Activators
  • pancreatic and duodenal homeobox 1 protein
  • Synaptotagmins
  • Luciferases