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KMID : 0360220080490060979
Journal of the Korean Ophthalmological Society
2008 Volume.49 No. 6 p.979 ~ p.986
Ischemic Preconditioning and the Role of Protein Kinase C in Cultured Retinal Ganglion Cell Line
Na Kyoung-Doo

Kang Sung-Yong
Seong Gong-Je
Hong Sa-Min
Chun Mi-Jin
Kim Chan-Yun
Abstract
Purpose: To investigate the cellular protective effects of hypoxic preconditioning against oxidative stress in a staurosporine-differentiated RGC-5 cell line and the relevance of protein kinase C subtype expression.

Methods: The minimum staurosporine concentration and exposure time necessary to morphologically fully differentiate RGC-5 cells were determined. Cytotoxic injury was provided by oxidative stress with 800 ¥ìM hydrogen peroxide (H2O2) for 15 hours to morphologically fully-differentiated cells. The cytoprotective effect of hypoxic preconditioning was found by exposing the cell line to 0.3% oxygen for different periods of time. Quantifiable changes in the expression of mRNAs and proteins of the isoenzymes ¥á, ¥â, ¥ã, ¥ä, ¥å, ¥æ of protein kinase C were determined before and after 1, 2, 15, and 24 hours of hypoxic preconditioning.

Results:Axonal growth in RGC-5 cells after the induction of differentiation with staurosporine caused these cells to resemble neurons. The minimal concentration and exposure time to staurosporine that evoked full differentiation of RGC-5 cells was exposure to 2 ¥ìM staurosporine for 1 hour. An LDH assay demonstrated that hypoxic preconditioning had neuroprotective effects against hydrogen peroxide-induced oxidative stress. Protein and mRNA levels of PKC isoforms ¥á and ¥å increased after preconditioning.

Conclusions:Hypoxic preconditioning of staurosporine-differentiated RGC-5 cells had a cytoprotective effect against oxidative stress. The associated increase of mRNA and proteins of PKC isoenzymes ¥á and ¥å suggest some functional relevance of these isoenzymes to the cytoprotective effects conferred by hypoxic preconditioning.
KEYWORD
Ischemic preconditioning, Oxidative stress, Protein kinase C, RGC-5
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