Apoptosis of interstitial cells of Cajal, smooth muscle cells, and enteric neurons induced by intestinal ischemia and reperfusion injury in adult guinea pigs

Virchows Arch. 2009 Apr;454(4):401-9. doi: 10.1007/s00428-009-0739-5. Epub 2009 Feb 12.

Abstract

This study aimed at evaluating whether apoptosis of interstitial cells of Cajal (ICC), smooth muscle cells (SMC), and enteric neurons was involved in a guinea pig model of intestinal ischemia and reperfusion injury. The small intestinal segments were resected at either 6 (I60/R6h) and 12 h (I60/R12h) or 7 (I60/R7d) to 14 (I60/R14d) days after 60 min intestinal ischemia in the adult guinea pigs and studied by immunohistochemistry with anti-Kit, 5-bromo-2'-deoxyuridine (BrdU), alpha-smooth muscle actin, vimentin, and beta-tublin III antibodies. Also, apoptosis was tested by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) method. In the I60/R12h injury, there was a approximately 50% decrease of Kit+ cells in cell numbers at the level of myenteric plexus and a number of Kit-/vimentin-positive cells were labeled by TUNEL. Also, a few SMC and enteric neurons were TUNEL positive. The Kit+ ICC recovered to normal and a number of Kit-/BrdU-double-positive cells were observed in the I60/R14d group. Our results indicated that the intestinal I/R injury could lead to apoptosis of ICC, SMC, and enteric neurons which may contribute to the gastrointestinal motility disorders, and proliferation was involved in the recovery of ICC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Apoptosis / physiology*
  • Fluorescent Antibody Technique
  • Guinea Pigs
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Intestinal Diseases / metabolism
  • Intestinal Diseases / pathology*
  • Intestines / blood supply
  • Intestines / innervation
  • Intestines / pathology
  • Myenteric Plexus / metabolism
  • Myenteric Plexus / pathology
  • Myocytes, Smooth Muscle / metabolism
  • Myocytes, Smooth Muscle / pathology*
  • Neurons / metabolism
  • Neurons / pathology*
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology*
  • Tubulin / metabolism
  • Vimentin / metabolism

Substances

  • Actins
  • Tubulin
  • Vimentin