Somatostatin stimulates colonic MUC2 expression through SSTR5-Notch-Hes1 signaling pathway

Biochem Biophys Res Commun. 2020 Jan 22;521(4):1070-1076. doi: 10.1016/j.bbrc.2019.11.034. Epub 2019 Nov 14.

Abstract

Colonic mucus barrier is regarded as the first defense line against bacteria and antigens from directly attaching to the epithelium, which would further lead to intestinal inflammation activation and pathological conditions. As MUC2 mucin is the predominant component of the mucus, understanding the regulatory mechanisms of MUC2 is important for mucus barrier protection. Somatostatin (SST) has been found to play a role in colon protection through various manners. However, whether SST involves in colonic mucus barrier regulation is still unclear. The aim of this study is to investigate the effects and potential mechanisms of SST on colonic MUC2 expression and mucus secretion. In vivo study, exogenous somatostatin (octreotide) administration effectively stimulated mice colonic MUC2 expression and mucus secretion. In human goblet-like cell LS174T cells, SST exposure also significantly stimulated MUC2 expression and mucus secretion. Further studies indicated that SST receptor 5 (SSTR5) was significantly activated by SST, whereas specific SSTR5 siRNA transfection of LS174T cells significantly blocked SST-induced increase in MUC2 expression and mucus secretion. In addition, SSTR5 agonist L817,818 also upregulated MUC2 expression and mucus secretion in LS174T cells. Mechanistic studies further demonstrated that SST/SSTR5-mediated MUC2 upregulation was dependent on Notch-Hes1 pathway suppression by detecting notch intracellular domain (NICD) and Hes1 proteins. Taken together, our findings suggested that SST could participate in colonic mucus barrier regulation through SSTR5-Notch-Hes1-MUC2 signaling pathway. These findings provide a deep insight into the role of SST on colonic mucus regulation under physiological conditions.

Keywords: MUC2; Mucus; Notch; Somatostatin; Somatostatin receptor 5.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Colon / metabolism*
  • Humans
  • Mice, Inbred C57BL
  • Mucin-2 / metabolism*
  • Mucus / metabolism
  • Octreotide / administration & dosage
  • Octreotide / pharmacology
  • Protein Binding / drug effects
  • Receptors, Notch / metabolism*
  • Receptors, Somatostatin / metabolism*
  • Signal Transduction*
  • Somatostatin / pharmacology*
  • Transcription Factor HES-1 / metabolism*
  • Up-Regulation / drug effects

Substances

  • Hes1 protein, mouse
  • Mucin-2
  • Receptors, Notch
  • Receptors, Somatostatin
  • Transcription Factor HES-1
  • Somatostatin
  • somatostatin receptor 5
  • Octreotide