Intramuscular interstitial cells of Cajal associated with mast cells survive nitrergic nerves in achalasia

Neurogastroenterol Motil. 2006 Jul;18(7):556-68. doi: 10.1111/j.1365-2982.2006.00788.x.

Abstract

Achalasia is dominated by injury to inhibitory nerves. As intramuscular interstitial cells of Cajal (ICC-IM) are proposed to form functional units with nitrergic nerves, their fate in achalasia may be critically important. We studied the relationship between loss of nitrergic nerves and injury to ICC-IM in patients with achalasia and determined associations between ICC-IM and mast cells (MC), using quantitative immunohistochemistry and electron microscopy. Loss of neuronal nitric oxide synthase (nNOS) immunoreactivity was completed within 3 years of acquiring achalasia. Thereafter, progressive ultrastructural injury to remaining nerve structures was evident. Within the first 2 years, the number of ICC-IM did not decline although ultrastructural injury was already present. Thereafter, loss of ICC-IM occurred unrelated to duration of disease. Damage to ICC-IM appeared unrelated to nerve injury. A significant MC infiltration was observed in the musculature; the number of MC was positively related to the persistent number of ICC-IM. Mast cell formed close contacts with ICC-IM and piecemeal-degranulation occurred towards ICC-IM. In conclusion, injury to ICC-IM in achalasia is variable, but not related to duration of disease and injury to nitrergic nerves. MC are prominent and form close functional contact with ICC-IM which may be responsible for their relatively long survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cell Communication / physiology
  • Esophageal Achalasia / immunology*
  • Esophageal Achalasia / pathology
  • Esophagus / cytology*
  • Esophagus / immunology*
  • Esophagus / innervation
  • Humans
  • Immunohistochemistry
  • Mast Cells / cytology*
  • Mast Cells / immunology
  • Mast Cells / metabolism
  • Microscopy, Electron, Transmission
  • Middle Aged
  • Muscle, Smooth / cytology
  • Muscle, Smooth / immunology
  • Muscle, Smooth / metabolism
  • Myenteric Plexus / metabolism
  • Myenteric Plexus / pathology
  • Nerve Degeneration
  • Nitrergic Neurons / metabolism
  • Nitrergic Neurons / pathology*
  • Nitric Oxide Synthase Type I / metabolism
  • Proto-Oncogene Proteins c-kit / metabolism

Substances

  • Nitric Oxide Synthase Type I
  • Proto-Oncogene Proteins c-kit