Oxidant-induced apoptosis in human retinal pigment epithelial cells: dependence on extracellular redox state

Invest Ophthalmol Vis Sci. 2005 Mar;46(3):1054-61. doi: 10.1167/iovs.04-0949.

Abstract

Purpose: To test whether variation in extracellular cysteine (Cys) redox potential (E(h)) over the physiologic range occurring in human plasma affects oxidant-induced apoptosis in cultured human retinal pigment epithelial (hRPE) cells.

Methods: The hRPE cells were incubated in culture medium with E(h) established over the range of -16 mV (most oxidized) to -158 mV (most reduced) by adding different concentrations of Cys and cystine (CySS) with constant total Cys equivalents. Apoptosis was induced with tert-butylhydroperoxide (tBH).

Results: The hRPE cells were sensitized to tBH-induced apoptosis in the more oxidized extracellular conditions (E(h) > -55 mV) compared with the reduced conditions (E(h) < -89 mV). Loss of mitochondrial membrane potential (Deltapsi(m)), release of cytochrome c, and activation of caspase 3 after tBH treatments all increased under the more oxidized conditions. However, the extracellular redox state did not affect expression of Fas or FasL in hRPE cells.

Conclusions: The hRPE cells that are exposed to a more oxidized extracellular redox environment have increased susceptibility to oxidant-induced apoptosis through the intrinsic mitochondrial pathway, which could contribute to an age-related decline in cell populations in the retina and thereby provide a potential mechanism for the degenerative changes that are associated with age-related macular degeneration (ARMD).

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspase 3
  • Caspases / metabolism
  • Cells, Cultured
  • Cysteine / pharmacology*
  • Cystine / pharmacology*
  • Cytochromes c / metabolism
  • Extracellular Space / physiology*
  • Fas Ligand Protein
  • Humans
  • In Situ Nick-End Labeling
  • Membrane Glycoproteins / metabolism
  • Membrane Potentials / drug effects
  • Mitochondria / drug effects
  • Oxidation-Reduction
  • Pigment Epithelium of Eye / metabolism
  • Pigment Epithelium of Eye / pathology*
  • fas Receptor / metabolism
  • tert-Butylhydroperoxide / toxicity

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • fas Receptor
  • Cystine
  • Cytochromes c
  • tert-Butylhydroperoxide
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Cysteine