医用臭氧对大鼠骨关节炎软骨细胞中PPARγ及自噬水平表达的影响

doi:10.6040/j.issn.1671-7554.0.2020.111

摘要/Abstract

摘要： 目的探讨医用臭氧对大鼠骨性关节炎软骨细胞中过氧化物酶体增殖物激活受体γ(PPARγ)及自噬相关蛋白表达的影响,及PPARγ在臭氧诱导的软骨细胞自噬中的作用。方法选取出生3 d以内的Wistar大鼠10只,获取四肢关节软骨进行原代软骨细胞的分离培养,并通过甲苯胺蓝染色及Ⅱ型胶原蛋白免疫荧光进行软骨细胞的鉴定。通过10 ng/mL 白介素-1β(IL-1β)刺激24 h构建骨关节炎软骨细胞模型。造模后采用不同浓度臭氧处理30 min,采用CCK-8法检测不同浓度臭氧对软骨细胞活力的影响,选出最佳臭氧浓度。造模后加入PPARγ特异性抑制剂GW9662处理12 h,再给予30 μg/mL臭氧处理。将原代软骨细胞随机分为对照组、模型组、模型臭氧组、正常臭氧组、模型臭氧+抑制剂组及模型抑制剂组。采用Western blotting法检测PPARγ蛋白及自噬相关蛋白LC3Ⅱ、P62及Beclin-1的表达。采用免疫荧光技术检测软骨细胞的自噬相关蛋白LC3B及P62的表达。结果经甲苯胺蓝染色及Ⅱ型胶原蛋白免疫荧光鉴定,分离培养的细胞为软骨细胞。不同浓度臭氧处理后,30 μg/mL臭氧处理后骨性关节炎软骨细胞的活力得到改善(P<0.05),50、70 μg/mL臭氧明显抑制骨性关节炎软骨细胞的活力(P<0.05)。30 μg/mL臭氧提高了骨性关节炎软骨细胞中PPARγ及自噬相关蛋白LC3Ⅱ及Beclin-1的表达水平,抑制了P62蛋白的表达(P<0.05)。PPARγ特异性抑制剂GW9662(20 mmol/mL)抑制臭氧对骨性关节炎软骨细胞自噬相关蛋白LC3Ⅱ、Beclin-1上调作用,并可逆转臭氧对P62的抑制作用。结论 30 μg/mL 医用臭氧可以促进骨性关节炎软骨细胞自噬,PPARγ激活在臭氧诱导骨性关节炎软骨细胞的自噬中起到促进作用。

关键词: 臭氧, 白介素-1β, 骨性关节炎, 过氧化物酶体增殖物激活受体γ, 自噬

Abstract: Objective To investigate the effects of ozone(O₃)on the expressions of peroxisome proliferators-activated receptor γ(PPARγ)and autophagy-related proteins in rat osteoarthritis chondrocytes and the role of PPARγ in ozone-induced autophagy of chondrocytes. Methods Wistar rats within 3 days of birth were chosen and the articular cartilage of extremities were obtained for the isolation and culture of primary chondrocytes. The chondrocytes were identified with toluidine blue staining and type II collagen immunofluorescence. The cells were stimulated with 10 ng/mL interleukin-1β(IL-1β)for 24 h to construct osteoarthritis chondrocytes models. After that, osteoarthritis chondrocytes were treated with different concentrations of ozone for 30 min, the effects on cell activity were detected by CCK-8 assay and the optimal O₃ concentration of 30 μg/mL was selected. After IL-1β treatment, PPARγ-specific inhibitor GW9662 was added to the osteoarthritis chondrocytes and treated for 12 h, which were then treated with 30 μg/mL O₃. The primary chondrocytes were randomly divided into control group, IL-1β group, IL-1β+O₃ group, control+O₃ group, IL-1β+O₃+GW9662 group and IL-1β+GW9662 group. The expressions of PPARγ and autophagy-related proteins including LC3 Ⅱ, P62 and Beclin-1 were detected with Western blotting. The expressions of LC3B and P62 were detected with immunofluorescence staining. Results Toluidine blue staining and type II collagen immunofluorescence identified the cultured cells were chondrocytes. The cell activity was improved with 30 μg/mL ozone(P<0.05), and decreased with 50 and 70 μg/mL ozone(P<0.05). The 30 μg/mL ozone increased the expressions of PPARγ, LC3Ⅱ and Beclin-1, while decreased the level of P62(P<0.05). GW9662(20 mmol/mL)inhibited the up-regulation effect of ozone on the levels of LC3Ⅱ and Beclin-1, and reversed the inhibition of ozone on P62. Conclusion Ozone at 30 μg/mL can promote autophagy of osteoarthritis chondrocytes, and activation of PPARγ can promote ozone-induced autophagy in osteoarthritis chondrocytes.

Key words: Ozone, Interleukin-1β, Osteoarthritis, peroxisome proliferators-activated receptors, peroxisome proliferators-activated receptors, Autophagy

中图分类号:

R575.1

孙盼盼,赵旭,林小雯,傅志俭. 医用臭氧对大鼠骨关节炎软骨细胞中PPARγ及自噬水平表达的影响[J]. 山东大学学报 (医学版), 2020, 58(6): 14-21.

SUN Panpan, ZHAO Xu, LIN Xiaowen, FU Zhijian. Effects of medical ozone on the expression of PPARγ and autophagy in chondrocytes of osteoarthritis in rats[J]. Journal of Shandong University (Health Sciences), 2020, 58(6): 14-21.

参考文献

[1] Shane Anderson A, Loeser RF. Why is osteoarthritis an age-related disease? [J]. Best Pract Res Clin Rheumatol, 2010, 24(1):15-26.
[2] Vinatier C, Dominguez E, Guicheux J, et al. Role of the inflammation-autophagy-senescence integrative network in osteoarthritis [J]. Front Physiol, 2018, 9:706-730. doi:10.3389/fphys.2018.00706.
[3] Ma F, Li G, Yu Y, et al. MiR-33b-3p promotes chondrocyte proliferation and inhibits chondrocyte apoptosis and cartilage ECM degradation by targeting DNMT3A in osteoarthritis[J]. Biochem Biophys Res Commun, 2019, 519(2):430-437.
[4] Luo P, Gao F, Niu D, et al. The role of autophagy in chondrocyte metabolism and osteoarthritis: a comprehensive research review[J]. Biomed Res Int, 2019,8:602-608. doi.org/10.1155/2019/5171602.
[5] Zhong J, Gong W, Chen J, et al. Micheliolide alleviates hepatic steatosis in db/db mice by inhibiting inflammation and promoting autophagy via PPAR-gamma-mediated NF-kB and AMPK/mTOR signaling[J]. Int Immunopharmacol, 2018, 59(4):197-208.
[6] Chen W, Xi X, Zhang S, et al. Pioglitazone protects against renal ischemia-reperfusion injury via the amp-activated protein kinase-regulated autophagy pathway[J].Front Pharmacol, 2018, 9(12):851-862.
[7] Vasheghani F, Zhang Y, Li YH, et al. PPARgamma deficiency results in severe, accelerated osteoarthritis associated with aberrant mTOR signalling in the articular cartilage[J]. Ann Rheum Dis, 2015, 74(3):569-578.
[8] Wang ZJ, Zhang HB, Chen C, et al. Effect of PPARG on AGEs-induced AKT/MTOR signaling-associated human chondrocytes autophagy[J]. Cell Biol Int, 2018, 42(7):841-848.
[9] Bhatia A, Munk P, Lee D, et al. Percutaneous ozone treatment for herniated lumbar discs: 1-year follow-up of a multicenter pilot study of a handheld disposable ozone-generating device[J]. J Vasc Interv Radiol, 2019, 30(5):752-760.
[10] Zhao X, Li Y, Lin X, et al. Ozone induces autophagy in rat chondrocytes stimulated with IL-1beta through the AMPK/mTOR signaling pathway[J]. J Pain Res, 2018, 11:3003-3017. doi:10.2147/jpr.s183594.
[11] Lotz MK,Caramés B. Autophagy and cartilage homeostasis mechanisms in joint health aging and OA[J].Nat RevRheumatol, 2011, 7(10):579-587.
[12] Houard X, Goldring MB, Berenbaum F. Homeostatic mechanisms in articular cartilage and role of inflammation in osteoarthritis[J]. Curr Rheumatol Rep, 2013, 15(11):375-393. doi:10.1007/s11926-013-0375-6.
[13] Manoto SL, Maepa MJ, Motaung SK. Medical ozone therapy as a potential treatment modality for regeneration of damaged articular cartilage in osteoarthritis[J]. Saudi J Biol Sci, 2018, 25(4): 672-679.
[14] 姜鹏, 李芸, 王珺楠, 等. 臭氧对骨性关节炎大鼠关节软骨Wnt/β-catenin 信号通路的影响[J]. 中华麻醉学杂志, 2016, 36(3):346-349. JIANG Peng, LI Yun, WANG Junnan, et al. Effect of ozone on Wnt/β-catenin signaling pathway in articular cartilage of rats with osteoarthritis[J]. Chin J Anesthesiol, 2016, 36(3):346-349.
[15] 于彦忠, 高俊霞. 不同浓度臭氧和玻璃酸钠关节腔内注射治疗膝关节骨关节炎[J]. 临床合理用药杂志,2015,8(20):65-66.
[16] Tontonoz P, Hu E, Spiegelman BM. Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor[J]. Cell, 1994, 79(7):1147-1156.
[17] Chawla A, Schwarz EJ, Dimaculangan DD, et al. Peroxisome proliferator-activated receptor(PPAR)gamma: adipose-predominant expression and induction early in adipocyte differentiation[J]. Endocrinology, 1994, 135(2):798-800.
[18] Li Z, Jia Y, Feng Y, et al. Methane-rich saline protects against sepsis-induced liver damage by regulating the PPAR-gamma/NF-kappaB signaling pathway[J]. Shock, 2019, 52(6): 163-172.
[19] Wang JS, Xiao WW, Zhong YS, et al. Galectin-3 deficiency protects lipopolysaccharide-induced chondrocytes injury via regulation of TLR4 and PPAR-gamma-mediated NF-kappaB signaling pathway[J]. J Cell Biochem, 2019, 120(6):10195-10204.
[20] Qu Y, Zhou L, Wang C. MangiferiniInhibits IL-1beta-induced inflammatory response by activating PPAR-gamma in human osteoarthritis chondrocytes[J]. Inflammation, 2017, 40(1):52-57.
[21] Wang ZJ, Zhang HB, Chen C, et al. Effect of PPARG on AGEs-induced AKT/MTOR signaling-associated human chondrocytes autophagy[J]. Cell Biol Int, 2018, 42(7):841-848.
[22] Dell'Accio F, Sherwood J. PPARgamma/mTOR signalling: striking the right balance in cartilage homeostasis[J]. Ann Rheum Dis, 2015, 74(3):477-479.
[23] Caramés B, Taniguchi N, Otsuki S, et al. Autophagy is a protective mechanism in normal cartilage and its aging-related loss is linked with cell death and osteoarthritis[J]. Arthritis Rheum, 2010, 62(3): 791-801.
[24] Meckes JK, Carames B, Olmer M, et al. Compromised autophagy precedes meniscus degeneration and cartilage damage in mice[J]. Osteoarthritis Cartilage, 2017, 25(11):1880-1889.
[25] Hill SM, Wrobel L, Rubinsztein DC. Post-translational modifications of Beclin 1 provide multiple strategies for autophagy regulation[J]. Cell Death Differ, 2019, 26(4):617-629.

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