Mast cell degranulation and parenchymal cell injury in the rat mesentery

J J Costa1, A G Harris, F A Delano

  • 1Institute for Biomedical Engineering and Department of Bioengineering, University of California, San Diego, La Jolla 92093-0412, USA.

Microcirculation (New York, N.Y. : 1994)
|September 29, 1999
PubMed
Abstract

Insights

Mast cell degranulation, triggered by compound 48/80 (CMP 48/80), causes mild parenchymal cell injury in rat mesentery even without leukocytes. Mast cell stabilization with Ketotifen prevented this injury.

Area of Science:

  • Physiology
  • Immunology
  • Microcirculation

Background:

  • Mast cells play a role in inflammatory responses.
  • Leukocyte adhesion is a key event in inflammation.
  • Parenchymal cell injury can result from inflammatory processes.

Purpose of the Study:

  • To investigate mast cell degranulation's effect on parenchymal cell injury.
  • To assess this injury in the absence of adherent leukocytes.
  • To determine the role of mast cells in mesenteric injury.

Main Methods:

  • Rats were made leukopenic using antibody treatment.
  • Intravital microscopy was used to superfuse the mesentery with compound 48/80 (CMP 48/80).
  • Propidium iodide (PI) assessed cell viability; Ketotifen stabilized mast cells.

Main Results:

  • CMP 48/80 caused a mild increase in parenchymal cell injury after leukocyte reduction.
  • Mesenteric injury levels significantly increased in specific regions.
  • Ketotifen treatment reduced injury below baseline levels.

Conclusions:

  • Mast cell degranulation contributes to mesenteric parenchymal cell injury.
  • This occurs even when leukocyte adhesion to the endothelium is absent.
  • Mast cells are implicated in direct tissue damage during inflammation.

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