Mitochondrial pathway of retinal pigment epithelial cell apoptosis induced by blue light in vitro

Authors: Li Hong,  Lyu Jianping,  Cai Shanjun,  Su Gang,  Wu Zhipeng,  Gong Xin
DOI: 10.3760/cma.j.issn.2095-0160.2015.01.004
Published 2015-01-10
Cite as Chin J Exp Ophthalmol, 2015,33(1): 16-20.

Abstract                              [Download PDF] [Read Full Text]

Background

Studies determined that blue light exposure causes apoptosis of human retinal pigment epithelial (RPE) cells, but its mechanism is still below understood.

Objective

The aim of this study was to investigate whether or how mitochondrial apoptotic pathway is involved in blue-light induced apoptosis of human RPE cells in vitro.

Methods

Human RPE cells were isolated from fresh donor eyes and primarily cultured and passaged.The cells were identified with keratin antibody by immunochemistry.Then the cells were the non-light exposed group, simple light-exposed group, light-exposed+nifedipine group, light-exposed+calphostin C group and the light-exposed+phorbol myristate acetate (PMA) group.Human RPE cells in light-exposed group were consequently cultured for 24 hours following the exposure of (2 000±500)lx blue-light for 6 hours, and then the expression levels of bax, bcl-2, bcl-xl in the cells were detected by Western blot to evaluate the effect of blue light on the apoptosis.The cells in the light-exposed+nifedipine group, light-exposed+calphostin C group and the light-exposed+PMA group were treated with the corresponding drugs 1 hour prior to light irradiation and sequently received 6-hour light irradiation and 48-hour culture.The expression of caspase-9 protein in the cells were assayed with Western blot to assess the influence of Ca2+ channel and protein kinase C (PKC) pathway on mitochondria of RPE cells.

Results

Cultured cells grew well with visible pigment in cytoplasm.The cells showed the positive response for keratin and presented a cobblestone-like appearance.The expression bands of bax, bcl-2 and bcl-xl proteins were clearly visible at the molecular weight of 23 000, 26 000 and 30 000 in both non-light exposed group and the simple light-exposed group, and the absorbance values of the cells to bax were elevated, while the absorbance values to bcl-2 and bcl-xl were declined in the simple light-exposed group compared with the non-light exposed group (t=-4.409, P=0.012;t=7.575, P=0.002;t=6.068, P=0.004).Compared with the non-light exposed group, the absorbance values of caspase-9 were significantly raised in the simple light-exposed group, light-exposed+calphostin C group and the light-exposed+PMA group (P=0.005, 0.002, 0.000), but no significant difference between the non-light exposed group and light-exposed+nifedipine group (P=0.191).Compared with the simple light-exposed group, the expression level was considerably higher in the light-exposed+PMA group (P=0.005);while that in the light-exposed+nifedipine group or light-exposed+calphostin C group was not significantly different (P=0.057, 0.643).

Conclusions

Blue light exposure induces apoptosis of RPE cells by up-regulating the expressions of bax and caspase-9 proteins and down-regulating the expressions of bcl-2 and bcl-xl. The mitochondrial apoptosis pathway and PKC pathway participate in blue-light induced apoptosis of human RPE cells in vitro.

Key words:

Blue light; Light-induced injury; Retinal pigment epithelium; Apoptosis; Mitochondria; Cysteine-aspartic acid proteases; Protein kinase C; Cell culture

Contributor Information

Li Hong
Department of Ophthalmology, Affiliated Hospital of Zunyi Medical College, Zunyi 563003, China
Lyu Jianping
Cai Shanjun
Su Gang
Wu Zhipeng
Gong Xin
(Read 25 times, 1 visits today)
Updated: June 8, 2023 — 9:51 am