首页|期刊导航|河北医学|miR-132-3p调控TLR4对颞下颌关节骨关节炎模型大鼠软骨细胞损伤的影响

miR-132-3p调控TLR4对颞下颌关节骨关节炎模型大鼠软骨细胞损伤的影响OA

The Effect of miR-132-3p Regulating TLR4 on Chondrocyte Injury in a Rat Model with Temporomandibular Joint Osteoarthritis

中文摘要英文摘要

目的:探讨 miR-132-3p 调控 Toll 样受体 4(TLR4)对颞下颌关节骨关节炎(TMJOA)模型大鼠软骨细胞损伤的影响.方法:大鼠随机分为假手术组、模型组,HE 染色检测 TMJ 髁突软骨组织病理变化;qRT-PCR 检 TMJ 软骨组织 miR-132-3p 及 TLR4 mRNA 表达.取假手术组和模型组各 2 只大鼠,分离右侧 TMJ 软骨细胞,假手术组分离的 TMJ 软骨细胞命名为对照组,模型组分离的 TMJ 软骨细胞分为 TMJOA 组、mimic NC 组、miR-132-3p mimic 组、miR-132-3p mimic+OE-NC 组、miR-132-3p mimic+OE-TLR4 组.qRT-PCR 检测细胞 miR-132-3p 及 TLR4 mRNA 表达;CCK-8、流式细胞术分别检测细胞活力、凋亡;ELISA 检测白细胞介素(IL)-10、IL-6、肿瘤坏死因子-α(TNF-α)水平;Western blot 检测 TMJ 软骨细胞 TLR4、聚集蛋白聚糖(Aggrecan)、Ⅱ型胶原蛋白(Collagen Ⅱ)蛋白;靶向关系验证.结果:与假手术组比较,模型组大鼠 TMJ 髁突软骨组织有炎性细胞浸润、软骨细胞排列紊乱、软骨层厚度变薄,TMJ 软骨组织 miR-132-3p 表达降低,TLR4 mRNA 表达升高(P<0.05).与对照组比较,TMJOA 组 TMJ 软骨细胞 miR-132-3p 表达、细胞活力、IL-10 水平及 Aggrecan、Collagen Ⅱ蛋白降低,TLR4 mRNA 和蛋白表达、细胞凋亡率、IL-6、TNF-α 水平升高(P<0.05);与 TMJOA 组、mimic NC 组比较,miR-132-3p mimic 组 TMJ 软骨细胞 miR-132-3p 表达、细胞活力、IL-10 水平及 Aggrecan、CollagenⅡ蛋白升高,TLR4 mRNA 和蛋白表达、细胞凋亡率、IL-6、TNF-α 水平降低(P<0.05);OE-TLR4 减弱了过表达 miR-132-3p 对 TMJOA 大鼠 TMJ 软骨细胞增殖、凋亡、ECM 降解及炎症的影响.miR-132-3p调控 TLR4.结论:过表达 miR-132-3p 可能通过靶向抑制 TLR4 促进 TMJOA 大鼠 TMJ 软骨细胞增殖,抑制细胞凋亡、ECM 降解及炎症.

Objective:To investigate the effect of miR-132-3p regulating Toll-like receptor 4(TLR4)on chondrocyte injury in a rat model of temporomandibular osteoarthritis(TMJOA).Methods:Rats were ran-domly divided into a sham operation group and a model group.HE staining was used to detect pathological changes of TMJ condylar cartilage tissue.The expressions of miR-132-3p and TLR4 mRNA in TMJ cartilage tissue were detected by qRT-PCR.Two rats were selected from each of the sham operation group and the model group,and right-sided TMJ chondrocytes were isolated.The TMJ chondrocytes isolated from the sham operation group were designated as the control group,whilst those from the model group were divided into the TMJOA group,the mimic NC group,the miR-132-3p mimic group,miR-132-3p mimic+OE-NC group,and miR-132-3p mimic+OE-TLR4 group.qRT-PCR was used to detect the expression of miR-132-3p and TLR4 mRNA in cells;CCK-8 and flow cytometry were used to assess cell viability and apoptosis,respec-tively;ELISA was used to measure levels of interleukin(IL)-10,IL-6 and tumour necrosis factor-α(TNF-α);Western blot was used to detect TLR4,aggrecan and collagen II in TMJ chondrocytes;and the targeting relationship was verified.Results:Compared with the sham operation group,the TMJ condylar cartilage tissue of rats in the model group showed inflammatory cell infiltration,disordered chondrocyte arrangement,thinner cartilage layer thickness,decreased miR-132-3p expression in TMJ cartilage tissue,and increased TLR4 mRNA expression(P<0.05).Compared with the control group,the expression of miR-132-3p,cell viabili-ty,IL-10 level,Aggrecan and Collagen II proteins in TMJ chondrocytes of the TMJOA group decreased,while the expression of TLR4 mRNA and protein,apoptosis rate,IL-6 and TNF-α levels increased(P<0.05).Compared with the TMJOA group and the mimic NC group,the expression of miR-132-3p,cell viabili-ty,IL-10 level,Aggrecan and Collagen II proteins in TMJ chondrocytes of the miR-132-3p mimic group in-creased.The expressions of TLR4 mRNA and protein,the apoptosis rate,and the levels of IL-6 and TNF-α decreased(P<0.05).OE-TLR4 weakened the promoting effect of overexpression of miR-132-3p on the proliferation of TMJ chondrocytes in TMJOA rats,as well as the inhibitory effects on apoptosis,ECM degrada-tion and inflammation.miR-132-3p targets and regulates TLR4.Conclusion:Overexpression of miR-132-3p may promote the proliferation of TMJ chondrocytes in TMJOA rats by targeting and inhibiting TLR4,and in-hibit apoptosis,ECM degradation,and inflammation.

张楠;蔡琦;李松;吴仲寅;焦国良

中国人民解放军联勤保障部队第九八〇医院口腔科,河北 石家庄 050000中国人民解放军联勤保障部队第九八〇医院口腔科,河北 石家庄 050000中国人民解放军联勤保障部队第九八〇医院口腔科,河北 石家庄 050000中国人民解放军联勤保障部队第九八〇医院口腔科,河北 石家庄 050000中国人民解放军联勤保障部队第九八〇医院口腔科,河北 石家庄 050000

骨关节炎miR-132-3pToll 样受体4颞下颌关节软骨细胞

OsteoarthritisMiR-132-3pToll-like receptor 4Temporomandibular jointChondrocyte

《河北医学》 2026 (5)

770-777,8

河北省医学科学研究课题计划资助(编号:20231300)

10.3969/j.issn.1006-6233.2026.05.010

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