The extracellular calcium-sensing receptor (CaSR) on human esophagus and evidence of expression of the CaSR on the esophageal epithelial cell line (HET-1A)

Am J Physiol Gastrointest Liver Physiol. 2008 Jan;294(1):G120-9. doi: 10.1152/ajpgi.00226.2006. Epub 2007 Oct 25.


Gastrointestinal reflux disease and eosinophilic esophagitis are characterized by basal cell hyperplasia. The extracellular calcium-sensing receptor (CaSR), a G protein-coupled receptor, which may be activated by divalent agonists, is expressed throughout the gastrointestinal system. The CaSR may regulate proliferation or differentiation, depending on cell type and tissue. The current experiments demonstrate the expression of the CaSR on a human esophageal epithelial cell line (HET-1A) and the location and expression of the CaSR in the human esophagus. CaSR immunoreactivity was seen in the basal layer of normal human esophagus. CaSR expression was confirmed in HET-1A cells by RT-PCR, immunocytochemistry, and Western blot analysis. CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). HET-1A cells transiently transfected with small interfering (si)RNA duplex against the CaSR manifested attenuated responses to Ca(2+) stimulation of phospho- (p)ERK1 and 2, [Ca(2+)](i) mobilization, and IL-8 secretion, whereas responses to acetylcholine (ACh) remained sustained. An inhibitor of phosphatidylinositol-specific phospholipase C (PI-PLC) (U73122) blocked CaSR-stimulated [Ca(2+)](i) release. We conclude that the CaSR is present on basal cells of the human esophagus and is present in a functional manner on the esophageal epithelial cell line, HET-1A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Blotting, Western
  • Calcium / metabolism
  • Calcium Signaling* / drug effects
  • Cell Line
  • Enzyme Activation
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism*
  • Esophagus / cytology
  • Esophagus / drug effects
  • Esophagus / metabolism*
  • Estrenes / pharmacology
  • Humans
  • Immunohistochemistry
  • Interleukin-8 / metabolism
  • Magnesium / metabolism
  • Microspectrophotometry
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Phosphodiesterase Inhibitors / pharmacology
  • Phosphorylation
  • Polymerase Chain Reaction
  • Pyrrolidinones / pharmacology
  • RNA Interference
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Receptors, Calcium-Sensing / genetics
  • Receptors, Calcium-Sensing / metabolism*
  • Spermine / metabolism
  • Transfection
  • Type C Phospholipases / antagonists & inhibitors
  • Type C Phospholipases / metabolism


  • CASR protein, human
  • Estrenes
  • Interleukin-8
  • Phosphodiesterase Inhibitors
  • Pyrrolidinones
  • RNA, Messenger
  • RNA, Small Interfering
  • Receptors, Calcium-Sensing
  • 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione
  • Spermine
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Type C Phospholipases
  • Magnesium
  • Acetylcholine
  • Calcium