Aims-To evaluate the effects of hydrogen peroxide exposure on the survival
and proliferation of cultured lens epithelial cells.
Methods-TOTL-86 cells, a line of rabbit lens epithelial cells, were used. T
he survival and proliferation of TOTL-86 cells were quantified by a rapid c
olorimetric assay (MTT assay). To determine the effects of hydrogen peroxid
e, TOTL-86 cells were exposed to different concentrations of hydrogen perox
ide, To determine the effect of cell numbers on the survival and proliferat
ion of TOTL-86 cells at a fixed concentration of hydrogen peroxide, differe
nt numbers of cells were plated and exposed to hydrogen peroxide, To determ
ine whether there is a synergistic effect between hydrogen peroxide and EGF
, bFGF, PDGF-AA, and insulin, TOTL-86 cells were exposed to hydrogen peroxi
de combined with one of these growth factors.
Results-High levels (1 mM) of hydrogen peroxide killed TOTL-86 cells and su
blethal levels (100 mu M) suppressed their proliferation. From 1 nM to 1 mu
M of hydrogen peroxide, there was a dose dependent increase in the cell nu
mbers. The initial seeded cell number dramatically affected the response to
hydrogen peroxide. Although growth factors showed no synergistic effects w
ith hydrogen peroxide on proliferation, both EGF and insulin, bur not bFGF
or PDGF, rescued TOTL-86 cells from the sublethal effect.
Conclusion-Hydrogen peroxide in cooperation with some growth factors plays
an important role in the proliferation of lens epithelial cell.