Blue LED light exposure develops intracellular reactive oxygen species, lipid peroxidation, and subsequent cellular injuries in cultured bovine retinal pigment epithelial cells

被引:61
作者
Nakanishi-Ueda, T. [1 ]
Majima, H. J. [2 ,3 ]
Watanabe, K. [1 ]
Ueda, T. [4 ]
Indo, H. P. [2 ,3 ]
Suenaga, S. [2 ,3 ]
Hisamitsu, T. [1 ]
Ozawa, T. [5 ]
Yasuhara, H. [6 ]
Koide, R. [6 ]
机构
[1] Showa Univ, Sch Med, Dept Physiol, Shinagawa Ku, Tokyo 1428555, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Oncol, Maxillofacial Radiol Div, Kagoshima 890, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Space Environm Med, Kagoshima 890, Japan
[4] Showa Univ, Sch Med, Dept Ophthalmol, Shinagawa Ku, Tokyo 142, Japan
[5] Yokohama Coll Pharm, Totsuka Ku, Yokohama, Kanagawa, Japan
[6] Showa Univ, Shinagawa Ku, Tokyo 1428555, Japan
关键词
reactive oxygen species; blue light hazard; retinal pigment epithelium; lipid peroxidation; INDUCED APOPTOSIS; GROWTH; LINE; MACULOPATHY; SENSITIVITY; PROTECTS; CANCER; MONKEY; DAMAGE; DEATH;
D O I
10.3109/10715762.2013.829570
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The effects of blue light emitter diode (LED) light exposure on retinal pigment epithelial cells (RPE cells) were examined to detect cellular damage or change and to clarify its mechanisms. The RPE cells were cultured and exposed by blue (470 nm) LED at 4.8 mW/cm(2). The cellular viability was determined by XTT assay and cellular injury was determined by the lactate dehydrogenase activity in medium. Intracellular reactive oxygen species (ROS) generation was determined by confocal laser microscope image analysis using dihydrorhodamine 123 and lipid peroxidation was determined by 4-hydroxy-2-nonenal protein-adducts immunofluorescent staining (HNE). At 24 h after 50 J/cm(2) exposures, cellular viability was significantly decreased to 74% and cellular injury was significantly increased to 365% of control. Immediately after the light exposure, ROS generation was significantly increased to 154%, 177%, and 395% of control and HNE intensity was increased to 211%, 359%, and 746% of control by 1, 10, and 50 J/cm(2), respectively. These results suggest, at least in part, that oxidative stress is an early step leading to cellular damage by blue LED exposure and cellular oxidative damage would be caused by the blue light exposure at even lower dose (1, 10 J/cm(2)).
引用
收藏
页码:774 / 780
页数:7
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