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中国精品科技期刊2020
谭敏颖,戴川景,卢学敏,等. 银耳多糖对人软骨细胞的增殖效应和抗炎作用[J]. 食品工业科技,2024,45(1):1−8. doi: 10.13386/j.issn1002-0306.2023060077.
引用本文: 谭敏颖,戴川景,卢学敏,等. 银耳多糖对人软骨细胞的增殖效应和抗炎作用[J]. 食品工业科技,2024,45(1):1−8. doi: 10.13386/j.issn1002-0306.2023060077.
TAN Minying, DAI Chuanjing, LU Xuemin, et al. Proliferation and Anti-inflammatory Effects of Tremella fuciformis Polysaccharide on Human Chondrocytes[J]. Science and Technology of Food Industry, 2024, 45(1): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023060077.
Citation: TAN Minying, DAI Chuanjing, LU Xuemin, et al. Proliferation and Anti-inflammatory Effects of Tremella fuciformis Polysaccharide on Human Chondrocytes[J]. Science and Technology of Food Industry, 2024, 45(1): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023060077.

银耳多糖对人软骨细胞的增殖效应和抗炎作用

Proliferation and Anti-inflammatory Effects of Tremella fuciformis Polysaccharide on Human Chondrocytes

  • 摘要: 目的:骨关节炎(Osteoarthritis,OA)是一种常见的慢性关节性疾病,本研究旨在探究银耳多糖对骨关节炎细胞模型人软骨细胞T/C-28a2的增殖效应和抗炎作用。方法:通过MTT(3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide)和结晶紫染色实验检测银耳多糖对T/C-28a2细胞增殖活力和细胞毒性的影响;用脂多糖(Lipopolysaccharide,LPS)处理T/C-28a2细胞建立骨炎症模型,酶联免疫吸附测定(Enzyme-linked immunosorbent assay,ELISA)检测药物处理后细胞白介素-6(Interleukin-6,IL-6)的表达;利用蛋白免疫印迹(Western blot)检测药物处理后相关骨保护因子和炎症因子的表达;通过ROS活性氧释放实验检测药物对细胞的氧化应激水平和抗炎症反应。结果:银耳多糖能够促进人软骨细胞T/C-28a2的增殖活力,且没有明显的细胞毒性;使用LPS刺激软骨细胞模拟骨炎症的环境,药物处理后发现银耳多糖和硫酸软骨素处理能减少IL-6分泌从而抑制炎症发生;进一步Western blot检测发现银耳多糖刺激后,相关骨保护因子(Osteoprotegerin,OPG)的表达上调,而促凋亡相关蛋白Bax、细胞外信号调节激酶(Extracellular-signal-regulated kinases,ERK-MAPK)和核内转录因子κB(Nuclear factor-kappaB,NF-κB)的表达下调。活性氧(Reactive oxygen species,ROS)释放实验结果显示,银耳多糖和硫酸软骨素能够抑制细胞内ROS水平,抑制炎症反应的发生。结论:银耳多糖具有抑制骨关节炎的效用,可以在一定程度上保护软骨组织,抵抗细胞凋亡。本研究初步探讨了银耳多糖的抗炎作用及机制,为开发银耳多糖作为抗炎药物提供初步的实验依据。

     

    Abstract: Objective: Osteoarthritis (OA) is a prevalent chronic joint disease. The purpose of this study was to investigate the proliferative and anti-inflammatory effects of Tremella fuciformis polysaccharide on osteoarthritis cell model human chondrocyte T/C-28a2. Methods: Proliferative effect and cytotoxicity of T/C-28a2 cells treated by Tremella fuciformis polysaccharide were detected with MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide) and crystal violet staining experiment. The bone inflammation model was established by lipopolysaccharide (LPS) treatment in T/C-28a2 cells. The expression of interleukin-6 (IL-6) in cells after drug treatment was detected by enzyme-linked immunosorbent assay (ELISA) analysis. The expression of osteoprotegerin (OPG) and inflammatory factors after drug treatment was detected by Western blot analysis. In addition, reactive oxygen species (ROS) release assay was used to detect the level of oxidative stress and anti-inflammation response to cells. Results: Tremella fuciformis polysaccharide could promote proliferation of human chondrocyte T/C-28a2 without obvious cytotoxicity. After LPS was used to treat human chondrocytes to simulate the environment of bone inflammation, it was found that the treatment of Tremella fuciformis polysaccharide and chondroitin sulfate could reduce the secretion of IL-6 and inhibit the occurrence of inflammation. Further Western blot analysis showed that after treatment of Tremella fuciformis polysaccharide, expression of related osteoprotegerin (OPG) was upregulated, expression of proapoptosis-related protein Bax, extracellular signal-regulated kinase ERK-MAPK and nuclear factor κB (NF-κB) was down-regulated. ROS release experiment showed that Tremella fuciformis polysaccharide and chondroitin sulfate could inhibit intracellular ROS levels and the occurrence of inflammatory response. Conclusion: Tremella fuciformis polysaccharide exhibited the effect of inhibiting osteoarthritis, protecting cartilage tissue and resisting cell apoptosis to a certain extent. In this study, the anti-inflammatory effect of Tremella fuciformis polysaccharide and its mechanism were primarily explored, which provided the preliminary experimental basis for the development of Tremella fuciformis polysaccharide as an anti-inflammatory drug.

     

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