Abstract

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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