Glucocorticoid-induced apoptosis of dendritic cells in the rat tracheal mucosa

Am J Respir Cell Mol Biol. 1998 Oct;19(4):598-605. doi: 10.1165/ajrcmb.19.4.2870.

Abstract

Dendritic cells are antigen-presenting cells that constitutively express high levels of major histocompatibility complex class II (Ia) antigen on their plasma membrane. Previous studies have shown that the number of dendritic cells in the rat airway mucosa decreases rapidly after glucocorticoid treatment. We sought to determine whether apoptosis contributes to this steroid-induced cell decrease. Dendritic cells in tracheal whole mounts were revealed by immunoperoxidase staining using the OX-6 (anti-Ia) monoclonal antibody. In untreated rats, a dense network of Ia-immunoreactive (Ia+) cells with highly branched cytoplasmic processes was observed just beneath the tracheal epithelium (1,405 +/- 140 cells/mm2 mucosa; mean +/- SEM, n = 6). In rats treated with dexamethasone (10 mg/kg, intraperitoneally), four distinct changes in dendritic cell morphology were evident 4 to 8 h after injection: (1) appearance of large Ia+ granules in cytoplasmic processes, (2) narrowing of cytoplasmic processes, (3) loss of Ia immunoreactivity from the cell surface, and (4) fragmentation of cells into small Ia+ bodies. These changes accompanied a 56% decrease in the number of Ia+ cells over 8 h. The contribution of apoptosis to this decrease in Ia+ cells was determined by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling (TUNEL) of nucleosomal DNA fragments in histologic sections. The number of TUNEL+ bodies increased from a control value of 174 +/- 47 bodies/mm2 mucosa to 2,108 +/- 294 bodies/mm2 mucosa at 4 h and 936 +/- 343 bodies/ mm2 mucosa at 8 h (n = 4 rats per time point). The location of TUNEL+ bodies closely corresponded to that of Ia+ cells stained in adjacent histologic sections. We conclude that apoptosis contributes to the rapid decrease in airway dendritic cells after glucocorticoid treatment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Apoptosis / drug effects*
  • Cell Count
  • Dendritic Cells / cytology*
  • Dendritic Cells / drug effects
  • Dexamethasone / pharmacology*
  • Glucocorticoids / pharmacology*
  • Histocompatibility Antigens Class II / immunology
  • Immunoenzyme Techniques
  • In Situ Nick-End Labeling
  • Male
  • Mucous Membrane / cytology
  • Rats
  • Rats, Wistar
  • Specific Pathogen-Free Organisms
  • Staining and Labeling / methods
  • Trachea / cytology*

Substances

  • Antibodies, Monoclonal
  • Glucocorticoids
  • Histocompatibility Antigens Class II
  • Dexamethasone