Abstract

The Munc-18 protein (mammalian homologue of the unc-18 gene; also called nSec1 or rbSec1) has been identified as an essential component of the synaptic vesicle fusion protein complex. The cellular and subcellular localization and functional role of Munc-18 protein in pancreatic beta-cells was investigated. Subcellular fractionation of insulin-secreting HIT-T15 cells revealed a 67-kDa protein in both cytosol and membrane fractions. Immunohistochemistry showed punctate Munc-18 immunoreactivity in the cytoplasm of rat pancreatic islet cells. Direct double-labeling immunofluorescence histochemistry combined with confocal laser microscopy revealed the presence of Munc-18 immunoreactivity in insulin-, glucagon-, pancreatic polypeptide-, and somatostatin-containing cells. Syntaxin 1 immunoreactivity was detected in extracts of HIT-T15 cells, which were immunoprecipitated using Munc-18 antiserum, suggesting an intimate association of Munc-18 with syntaxin 1. Administration of Munc-18 peptide or Munc-18 antiserum to streptolysin O-permeabilized HIT-T15 cells resulted in significantly increased insulin release, but did not have any significant effect on voltage-gated Ca(2+) channel activity. The findings taken together show that the Munc-18 protein is present in insulin-secreting beta-cells and implicate Munc-18 as a negative regulator of the insulin secretory machinery via a mechanism that does not involve syntaxin-associated Ca(2+) channels.

Highlights

  • The Munc-18 protein has been identified as an essential component of the synaptic vesicle fusion protein complex

  • We have investigated the cellular localization of Munc-18 at the protein level in pancreatic endocrine cells using subcellular fractionation combined with Western blotting as well as immunohistochemistry combined with confocal laser microscopy

  • Our results show that the Munc-18 protein is present in pancreatic ␤-cells, that Munc-18 is associated with the t-SNARE syntaxin in insulin-producing cells, and that Munc-18 has a regulatory role in insulin exocytosis via a mechanism not involving voltage-gated Ca2ϩ channels

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Summary

Introduction

The Munc-18 protein (mammalian homologue of the unc-18 gene; called nSec1 or rbSec1) has been identified as an essential component of the synaptic vesicle fusion protein complex. Administration of Munc-18 peptide or Munc-18 antiserum to streptolysin O-permeabilized HIT-T15 cells resulted in significantly increased insulin release, but did not have any significant effect on voltage-gated Ca2؉ channel activity. The effect of Munc-18 peptide and Munc-18 antiserum on insulin release was studied in streptolysin O-permeabilized insulin-secreting HIT-T15 cells.

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