Delta-like 1 expression promotes goblet cell differentiation in Notch-inactivated human colonic epithelial cells

Biochem Biophys Res Commun. 2010 Mar 19;393(4):662-7. doi: 10.1016/j.bbrc.2010.02.048. Epub 2010 Feb 17.

Abstract

Notch signaling has previously been implicated in the regulation of the cell fate of intestinal epithelial cells. However, the expression and function of Notch ligands in the human intestine remain largely unknown. In the present study, we showed that Notch ligands Delta-like 1 (Dll1) and Delta-like 4 (Dll4) are expressed in a goblet cell-specific manner in human colonic tissue. Additionally, we found that Dll1 and Dll4 expression was regulated in-parallel with Atoh1 and MUC2, which are both under the control of the Notch-Hes1 signaling pathway. Because knockdown of Dll1 expression completely abrogated the acquisition of the goblet cell phenotype in Notch-inactivated colonic epithelial cells, we postulate that Dll1 might function as a cis-acting regulatory element that induces undifferentiated cells to become goblet cells. Our results suggest a link between Dll1 expression and human goblet cell differentiation that might be mediated by a function that is distinct from its role as a Notch receptor ligand.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Calcium-Binding Proteins
  • Cell Differentiation*
  • Cells, Cultured
  • Colon / cytology*
  • Colon / metabolism
  • Gene Knockdown Techniques
  • Goblet Cells / cytology*
  • Goblet Cells / metabolism
  • Homeodomain Proteins / metabolism
  • Humans
  • Intercellular Signaling Peptides and Proteins / biosynthesis*
  • Intercellular Signaling Peptides and Proteins / genetics
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / genetics
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Signal Transduction
  • Transcription Factor HES-1
  • Up-Regulation

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Calcium-Binding Proteins
  • DLK1 protein, human
  • Homeodomain Proteins
  • Intercellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Receptors, Notch
  • Transcription Factor HES-1
  • HES1 protein, human