Bcl-2 sustains increased mucous and epithelial cell numbers in metaplastic airway epithelium

Am J Respir Crit Care Med. 2005 Apr 1;171(7):764-72. doi: 10.1164/rccm.200408-1108OC. Epub 2004 Dec 23.

Abstract

Bcl-2, an inhibitor of apoptosis, is expressed in LPS-induced metaplastic goblet cells of rat airways. The present study investigated expression of Bcl-2 in airway mucous cells of persons with cystic fibrosis and tested in rats and mice whether its expression is responsible for sustaining metaplastic mucous cells. A significantly higher percentage of mucous cells expressed Bcl-2 in humans with cystic fibrosis compared with control subjects with no disease or subjects with other diseases. In LPS-instilled F344/N rats, the percentage of Bcl-2-positive mucous cells was decreased to background levels before the resolution of goblet cell metaplasia. Furthermore, intraperitoneal injection of rats with antisense oligonucleotides significantly reduced Bcl-2 expression and goblet cell metaplasia in nasal and pulmonary airway epithelia in rats. In contrast, sustained expression of Bcl-2 in transgenic mice by a metallothionein promoter caused increased LPS-induced goblet cell metaplasia over 8 days compared with wild-type mice. These studies demonstrate that Bcl-2 expression sustains goblet cell metaplasia in various species, that epithelial cell numbers are directly linked to the regulation of the numbers of goblet cells, and that downregulating Bcl-2 expression reduces goblet cell metaplasia.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Animals
  • Apoptosis / physiology*
  • Base Sequence
  • Case-Control Studies
  • Cystic Fibrosis / metabolism
  • Cystic Fibrosis / pathology*
  • Epithelial Cells / cytology*
  • Epithelial Cells / drug effects
  • Female
  • Gene Expression Regulation
  • Humans
  • Male
  • Molecular Sequence Data
  • Nasal Mucosa / metabolism*
  • Nasal Mucosa / physiology
  • Oligonucleotides, Antisense / pharmacology*
  • Organ Culture Techniques
  • Polymerase Chain Reaction
  • Probability
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Rats
  • Rats, Inbred F344
  • Reference Values
  • Sensitivity and Specificity
  • Species Specificity
  • Up-Regulation

Substances

  • Oligonucleotides, Antisense
  • Proto-Oncogene Proteins c-bcl-2