首页 | 本学科首页   官方微博 | 高级检索  
     

氧化应激相关细胞衰老指标与骨关节炎的相关性探讨
引用本文:曹娟,李玲玲,姚瑶,肖云云,武文卉,陆邦超,丁从珠. 氧化应激相关细胞衰老指标与骨关节炎的相关性探讨[J]. 中华全科医学, 2023, 21(3): 396-400. DOI: 10.16766/j.cnki.issn.1674-4152.002892
作者姓名:曹娟  李玲玲  姚瑶  肖云云  武文卉  陆邦超  丁从珠
作者单位:1.南京大学医学院附属鼓楼医院老年医学科,江苏 南京 210009
基金项目:南京市医学科技发展重点项目ZKX17020江苏省干部保健科研课题BJ19003
摘    要:目的 通过检测软骨细胞衰老相关指标,探讨软骨细胞衰老与骨关节炎(OA)发病的相关性。方法 选取2018年1月—2020年12月南京鼓楼医院骨科需手术住院的OA患者及非OA患者各6例,分离培养膝关节软骨细胞,分为正常软骨细胞组(对照组)、OA软骨细胞组(OA组),选P2代细胞分别进行β-半乳糖苷酶染色检测,收集细胞行流式细胞仪检测细胞活性氧(ROS)水平、线粒体膜电位,定量PCR(qPCR)检测细胞P21、P53基因mRNA表达,采用Western blotting检测软骨细胞中P21、P53蛋白水平。结果 OA组软骨细胞β-半乳糖苷酶染色阳性率显著增高,OA组ROS水平[(24.72±2.40)%]较对照组[(4.96±0.14)%]明显升高(P<0.01),OA组JC-1染色绿色荧光强度[(21.87±3.03)%]即细胞线粒体膜电位下降明显高于对照组[(3.13±0.25)%,P<0.01];OA组P21、P53基因mRNA表达量(2.72±0.21、2.90±0.23),较对照组表达量(1.00±0.03、1.00±0.06)显著增加(均P<0.05)。OA组周...

关 键 词:骨关节炎  软骨细胞衰老  氧化应激
收稿时间:2022-07-02

Correlation between oxidative stress related cell senescence indicators and osteoarthritis
Affiliation:Department of Geriatrics, Drum Tower Hospital Affiliated Nanjing University Medical College, Nanjing, Jiangsu 210009, China
Abstract:  Objective  To investigate the correlation between chondrocyte senescence and osteoarthritis (OA) by detecting chondrocyte senescence related indicators.  Methods  The OA patients and non-OA patients hospitalized in the Department of Orthopedics in Nanjing Drum Tower Hospital were selected from January 2018 to December 2020. Normal knee chondrocytes and OA knee chondrocytes were isolated and cultured, and divided into normal human chondrocytes group (control group) and OA chondrocytes group (OA group). P2 generation cells were selected for the experiment. β galactosidase staining was performed. The reactive oxygen species (ROS) level and mitochondrial membrane potential were detected by flow cytometry. The mRNA expressions of P21 and P53 genes were detected by quantitative PCR (qPCR), and the protein levels of P21 and P53 in chondrocytes were detected by Western blotting.  Results  The positive rate of β-galactosidase staining in chondrocytes in the OA group was significantly higher than that in the control group. The level of ROS in the OA group [(24.72±2.40) %] was significantly higher than that in the control group [(4.96±0.14) %, P < 0.01]. The green fluorescence intensity of JC-1 staining in the OA group [(21.87±3.03) %] was significantly higher than that in the control group [(3.13±0.25) %, P < 0.01]. The mRNA expressions of P21 and P53 genes in the OA group were (2.72±0.21) and (2.90±0.23), which were significantly higher than those in the control group (1.00±0.03) and (1.00±0.06), all P < 0.05. The expression levels of cyclin P21 and P53 in the OA group [(0.51±0.02) and (0.55±0.03)] were also significantly higher than those in the control group [(0.40±0.03) and (0.45±0.02), P < 0.01].  Conclusion  Compared with normal chondrocytes, OA chondrocytes senesce significantly. Oxidative stress-induced cell senescence may play a key role in the pathogenesis of OA. Anti-oxidative stress may be an effective target for the treatment of OA. 
Keywords:
点击此处可从《中华全科医学》浏览原始摘要信息
点击此处可从《中华全科医学》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号