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TLR4/NF-κB通路参与大鼠膝骨关节炎滑膜早期病变的研究
Hits: 1901   Download times: 1063   Received:October 30, 2018    
作者Author单位UnitE-Mail
王学宗 WANG Xue-zong 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203
上海市中医药研究院骨伤科研究所, 上海 201203
Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China  
丁道芳 DING Dao-fang 上海市中医药研究院骨伤科研究所, 上海 201203  
薛艳 XUE Yan 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203 Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China  
顾新丰 GU Xin-feng 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203 Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China  
庞坚 PANG Jian 上海市中医药研究院骨伤科研究所, 上海 201203  
张旻 ZHANG Min 上海市中医药研究院骨伤科研究所, 上海 201203  
郑昱新 ZHENG Yu-xin 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203 Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China sg_zyx1728@126.com 
曹月龙 CAO Yue-long 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203
上海市中医药研究院骨伤科研究所, 上海 201203
Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China  
詹红生 ZHAN Hong-sheng 上海中医药大学附属曙光医院石氏伤科医学中心, 上海 201203
上海市中医药研究院骨伤科研究所, 上海 201203
Shi's Center of Orthopaedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China  
期刊信息:《中国骨伤》2019年32卷,第1期,第68-71页
DOI:10.3969/j.issn.1003-0034.2019.01.015
基金项目:国家自然科学基金(编号:81503598;81503592;81674003;81774340);上海市进一步加快中医药事业发展三年行动计划(编号:ZY3-LCPT-2-1005)


目的:探讨TLR4/NF-κB通路在大鼠膝骨关节炎(OA)滑膜早期病变的表达情况。

方法:将8周龄体重为(200±20)g的18只雄性SD大鼠按照随机数字表法分为模型组和对照组,每组9只。模型组按照改良Hulth法构建膝OA模型,对照组不做手术。分别于术后4、21 d提取滑膜组织和血清,采用PCR法检测CD14、TLR-4、IL-1β、TNF-α、MMP-13、ADAMTS-4表达;采用Western-blot法检测NF-κB p65蛋白表达;采用Elisa法检测血清中透明质酸(HA)及Ⅲ型前胶原氨基端(PⅢNP)浓度。

结果:术后4、21 d时模型组CD14、ADAMTS-4及NF-κB p65表达均较对照组升高,术后21 d时模型组TLR-4、Ⅱ-1β、TNF-α及MMP-13表达较对照组升高(P<0.01)。模型组术后4 d时血清PⅢNP和HA浓度高于对照组,术后21 d时两组比较差异无统计学意义。

结论:NF-κB通路可通过CD14/TLR-4早期激活进而触发滑膜分泌炎性因子IL-1β、TNF-a、MMP-13、ADAMTS-4,PⅢNP和HA增加介导膝OA发生。
[关键词]:骨关节炎,膝  滑膜  大鼠
 
Role of TLR4/NF-κB pathway for early change of synovial membrane in knee osteoarthritis rats
Abstract:

Objective: To study role of TLR4/NF-κB pathway for early change of synovial membrane in knee osteoarthritis rats.

Methods: Eighteen male SD rats weighted (200±20) g were randomly divided into 2 groups,namely control and model group,and 9 in each group. Knee OA model group was established by using modified Hulth method in model group. Control group was not treated. Synovial tissue and serum was extracted at 4 and 21 d after operation. Expression of CD14,TLR4,IL-1β,TNF-α,ADAMTS-4,MMP-13 were detected by real-time PCR respectively. NF-κB p65 protein was detected by Western-blot;serum concentrations of haluronic acid (HA),N-propeptide of type Ⅲ procollagen(PⅢNP) was detected by Elisa.

Results: Expression of CD14,ADAMTS-4,and NF-κB p65 in model group were higher than that of control group at 4 and 21 days after operation,while expression of TLR4,IL-1β,TNF-α and MMP-13 were higher than that of control group at 21 days after operation(P<0.01). Concentration of PⅢNP and HA in model group were higher than that of control group at 4 days after operation,while there was no significant difference at 21 days after operation.

Conclusion: NF-κB pathway could mediate occurrence of KOA by early activating and triggeringg synovial increasingly secreting inflammatory secretion CD14,TLR4,IL-1β,TNF-α,ADAMTS-4,MMP-13,PⅢNP and HA.
KEYWORDS:Osteoarthritis,knee  Synovial membrane  Rats
 
引用本文,请按以下格式著录参考文献:
中文格式:王学宗,丁道芳,薛艳,顾新丰,庞坚,张旻,郑昱新,曹月龙,詹红生.TLR4/NF-κB通路参与大鼠膝骨关节炎滑膜早期病变的研究[J].中国骨伤,2019,32(1):68~71
英文格式:WANG Xue-zong,DING Dao-fang,XUE Yan,GU Xin-feng,PANG Jian,ZHANG Min,ZHENG Yu-xin,CAO Yue-long,ZHAN Hong-sheng.Role of TLR4/NF-κB pathway for early change of synovial membrane in knee osteoarthritis rats[J].zhongguo gu shang / China J Orthop Trauma ,2019,32(1):68~71
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