Granuphilin is activated by SREBP-1c and involved in impaired insulin secretion in diabetic mice

Cell Metab. 2006 Aug;4(2):143-54. doi: 10.1016/j.cmet.2006.06.009.

Abstract

Granuphilin is a crucial component of the docking machinery of insulin-containing vesicles to the plasma membrane. Here, we show that the granuphilin promoter is a target of SREBP-1c, a transcription factor that controls fatty acid synthesis, and MafA, a beta cell differentiation factor. Potassium-stimulated insulin secretion (KSIS) was suppressed in islets with adenoviral-mediated overexpression of granuphilin and enhanced in islets with knockdown of granuphilin (in which granuphilin had been knocked down). SREBP-1c and granuphilin were activated in islets from beta cell-specific SREBP-1c transgenic mice, as well as in several diabetic mouse models and normal islets treated with palmitate, accompanied by a corresponding reduction in insulin secretion. Knockdown- or knockout-mediated ablation of granuphilin or SREBP-1c restored KSIS in these islets. Collectively, our data provide evidence that activation of the SREBP-1c/granuphilin pathway is a potential mechanism for impaired insulin secretion in diabetes, contributing to beta cell lipotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism*
  • Insulin / metabolism*
  • Insulin Secretion
  • Islets of Langerhans / metabolism
  • Maf Transcription Factors, Large / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Mice, Transgenic
  • Palmitates / pharmacology
  • Palmitates / toxicity
  • Potassium / pharmacology
  • Promoter Regions, Genetic / drug effects
  • Signal Transduction
  • Sterol Regulatory Element Binding Protein 1 / metabolism
  • Sterol Regulatory Element Binding Protein 1 / pharmacology*
  • Vesicular Transport Proteins / drug effects
  • Vesicular Transport Proteins / genetics*
  • Vesicular Transport Proteins / metabolism*

Substances

  • Insulin
  • Maf Transcription Factors, Large
  • Mafa protein, mouse
  • Palmitates
  • Srebf1 protein, mouse
  • Sterol Regulatory Element Binding Protein 1
  • Sytl4 protein, mouse
  • Vesicular Transport Proteins
  • Potassium