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Effects of oxidative damage on selenoprotein gene expression in articular chondrocytes and the mechanism of selenium

硫氧还蛋白还原酶 化学 细胞凋亡 软骨细胞 氧化应激 硒蛋白 细胞生物学 GPX1型 谷胱甘肽 分子生物学 硒缺乏症 基因表达 内科学 软骨 男科 生物化学 过氧化氢酶 谷胱甘肽过氧化物酶 硒蛋白P 生物 医学 有机化学
作者
Rongqiang Zhang,Xiaoli Yang,Yongmin Xiong,Lixin Han,Yong Jiang,Ziyun Shi,Mingming Pan,Junling Cao
出处
期刊:Chin J Endemiol 卷期号:36 (9): 648-652
标识
DOI:10.3760/cma.j.issn.2095-4255.2017.09.006
摘要

Objective To explore the effects of oxidative damage and selenium on the apoptosis of articular chondrocytes and the expression of selenoprotein genes. Methods C28/I2 chondrocytes were preincubated for 24 h, using sodium selenite (Na2SeO3) or t-butyl hydroperoxide (tBHP) for 24 h. The experiment was divided into six groups, including control group (C, 0.00 mg/L Na2SeO3+ 0.00 μmol/L tBHP), selenium beforehand protection group (S2, 0.10 mg/L Na2SeO3), oxidative damage group (O, 150.00 μmol/L tBHP), low dose selenium protection group (OS1, 0.05 mg/L Na2SeO3+ 150.00 μmol/L tBHP), medium dose selenium protection group (OS2, 0.10 mg/L Na2SeO3+ 150.00 μmol/L tBHP), and high dose selenium protection group (OS3, 0.15 mg/L Na2SeO3+ 150.00 μmol/L tBHP). After 24 h, Hoechst 33342 staining method was used to observe apoptosis, mRNA expression of glutathione peroxidase 1 (GPX1), GPX4, deiodinase 2 (DIO2), DIO3, selenoprotein P (SEPP1), thioredoxin reductase 1 (TrxR-1) and selenoprotein W(Sel W) was detected by Real-time PCR, both experiments were done three times. Results Apoptotic rates of C, S2, O, OS1, OS2, OS3 groups [(0.78 ± 0.06)%, (13.61 ± 7.11)%, (92.27 ± 3.44)%, (71.38 ± 5.22)%, (44.31 ± 9.16)%, (72.46 ± 4.69)%] were compared between groups, the differences were statistically significant (F= 120.10, P < 0.01). The apoptotic rates of O group was significantly higher than that of C group (P < 0.05); compared to O group, the apoptotic rates of OS1, OS2, OS3 groups decreased significantly (P < 0.05), OS2 group was the most obvious. DIO2, SEPP1, GPX1, GPX4, TrxR-1, Sel W mRNA levels were compared in the six groups, the differences were statistically significant (F= 24.60, 14.53, 127.60, 30.60, 637.10, 59.64, P < 0.01). Compared to C group (1.00 ± 0.00), the mRNA levels of GPX1 (0.10 ± 0.05), GPX4 (0.43 ± 0.09), TrxR-1 (0.11 ± 0.05) and Sel W (0.72 ± 0.15) in O groups were decreased significantly (P < 0.05); compared to O group, the mRNA levels of GPX1 in OS1 (0.20 ± 0.03), OS2 (0.74 ± 0.10), and OS3 (0.30 ± 0.07) were increased significantly (P < 0.05). Conclusion Down-regulated expression of selenoprotein genes are involved in the regulation process of articular cartilage apoptosis caused by oxidative stress, selenium also has a regulatory role in selenoprotein gene expression in articular chondrocytes. Key words: Chondrocytes; Selenoproteins; Sodium selenite
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