Aqueous humor-borne factor upregulates Bcl-2 expression in corneal endothelial cells

Curr Eye Res. 1998 Oct;17(10):970-8. doi: 10.1076/ceyr.17.10.970.5240.

Abstract

Purpose: To determine if factors present in the aqueous humor (AH) protect the corneal endothelium from apoptosis.

Methods: Mouse and human corneal endothelial cells were cultured in vitro, and apoptosis was induced by nutrient deprivation. AH and supernatant from iris/ciliary body (I/CB) cell cultures were tested for their effect on corneal endothelial cell apoptosis. The effect of I/CB supernatant on Fas, Bax, and Bcl-2 gene transcription was evaluated by Northern blotting. I/CB supernatant was subjected to proteinase analysis to identify the apoptosis inhibitory factor(s).

Results: Rabbit AH and supernatant from mouse I/CB cell cultures inhibited the apoptosis of mouse and human immortalized corneal endothelial cell lines. The inhibition of apoptosis was associated with an upregulation of Bcl-2 gene transcription and Bcl-2 protein expression. Bax gene expression was not significantly affected by I/CB cell supernatant. Induction of apoptosis by stimulation of the Fas receptor was unaffected by I/CB cell supernatant. Protease analyses indicated that the apoptosis inhibitory factor was a protein.

Conclusions: The inability of corneal endothelial cells to undergo mitosis renders the corneal endothelium vulnerable to loss of physiological function through cellular attrition. However, a protein(s) produced by I/CB cells and present in the AH, upregulates Bcl-2 gene transcription and protects the corneal endothelial cells from apoptosis.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Aqueous Humor / physiology*
  • Biological Factors / physiology*
  • Blotting, Northern
  • Cells, Cultured
  • Ciliary Body / cytology
  • Ciliary Body / physiology
  • DNA / analysis
  • DNA Primers / chemistry
  • DNA Probes
  • Endothelium, Corneal / metabolism*
  • Fluorescent Antibody Technique, Indirect
  • Genes, bcl-2 / genetics
  • Humans
  • In Situ Nick-End Labeling
  • Iris / cytology
  • Iris / physiology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Inbred NZB
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Rabbits
  • Receptors, Tumor Necrosis Factor / metabolism
  • Up-Regulation
  • bcl-2-Associated X Protein
  • fas Receptor

Substances

  • BAX protein, human
  • Bax protein, mouse
  • Biological Factors
  • DNA Primers
  • DNA Probes
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Tumor Necrosis Factor
  • bcl-2-Associated X Protein
  • fas Receptor
  • DNA