Inhibition of DNA methyltransferase or histone deacetylase protects retinal pigment epithelial cells from DNA damage induced by oxidative stress by the stimulation of antioxidant enzymes

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• 作者：Paulina Tokarz^a ; ^{ptokarz@biol.uni.lodz.pl" class="auth_mail" title="E-mail the corresponding author} ; Kai Kaarniranta^b ; ^c ; ^{Kai.Kaarniranta@kuh.fi" class="auth_mail" title="E-mail the corresponding author} ; Janusz Blasiak^a ; ^{jblasiak@biol.uni.lodz.pl" class="auth_mail" title="E-mail the corresponding author}
• 关键词：RG108 (PubChem CID ; 702558) ; Tert-butyl hydroperoxide (PubChem CID ; 6410) ; Valproic acid (PubChem CID ; 3121)
• 刊名：European Journal of Pharmacology
• 出版年：2016
• 出版时间：5 April 2016
• 年：2016
• 卷：776
• 期：Complete
• 页码：167-175
• 全文大小：1573 K

文摘

Epigenetic modifications influence DNA damage response (DDR). In this study we explored the role of DNA methylation and histone acetylation in DDR in cells challenged with acute or chronic oxidative stress. We used retinal pigment epithelial cells (ARPE-19), which natively are exposed to oxidative stress due to permanent exposure to light and high blood flow. We employed a DNA methyltransferase inhibitor – RG108 (RG), or a histone deacetylase inhibitor – valproic acid (VA). ARPE-19 cells were exposed to tert-butyl hydroperoxide, an acute oxidative stress inducer, or glucose oxidase, which slowly liberates low-doses of hydrogen peroxide in the presence of glucose, creating chronic conditions. VA and RG reduced level of intracellular reactive oxygen species and DNA damage in ARPE-19 cells in normal condition and in oxidative stress. This protective effect of VA and RG was associated with the up-regulated expression of antioxidant enzyme genes: CAT, GPx1, GPx4, SOD1 and SOD2. RG decreased the number of cells in G2/M checkpoint in response to chronic oxidative stress. Neither RG nor VA changed the DNA repair or apoptosis induced by oxidative stress. Therefore, certain epigenetic manipulations may protect ARPE-19 cells from detrimental effects of oxidative stress by modulation of antioxidative enzyme gene expression, which may be further explored in pharmacological studies on oxidative stress-related eye diseases.