Downregulation of IL-11 regulates the TGFβ/ERK1/2 signaling pathway to inhibit articular capsule fibrosis and alleviate post-traumatic articular capsule contracture.

IF 2.9 2区 医学 Q1 ORTHOPEDICS
Heng Zheng, Zhen-Jia Zhong, Yi-Chong Wang, Yang-Bai Sun, Feng-Feng Li
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引用次数: 0

Abstract

Background: Post-traumatic capsular contracture is a common complication of joint injury and surgery. Post-traumatic capsular contracture is associated with fibrosis characterized by excessive differentiation and proliferation of myofibroblasts and abnormal secretion and accumulation of extracellular matrix. Previous studies have suggested that IL11 plays a role in myocardial fibrosis. We thus hypothesized that IL11 may play a fibrotic role during capsular contracture, in order to discover new targets for preventing joint capsule contracture METHODS: We constructed a post-traumatic contracture model by excessively extending the knee joint and fixing the joint in the flexion position, and a post-traumatic joint capsule contracture model was constructed in the wild-type, IL11-/-, IL11R -/-, α-SMA-cre-IL11fl/fl, α-SMA-cre-IL11Rfl/fl mouse strain, with wild-type mice without any treatment of the knee joint as the control group. Fibrotic markers and the expression of IL11 and IL11R in knee joint tissue were detected in each group of mice. The NIH3T3 cell line was used for in vitro analyses. The expression of fibrosis markers, IL11, TGFβ and ERK1/2 were detected by western blot, ELISA and RT-qPCR.

Results: Inhibition of IL11 inhibited ERK1/2 phosphorylation, reduced the secretion of collagen in the joint capsule, and inhibited the excessive differentiation and proliferation of myofibroblasts in the post-traumatic joint capsule contracture, thus alleviating the joint capsule contracture and obtaining better joint mobility.

Conclusion: Downregulation of IL11 in traumatic joint capsule contracture inhibits ERK1/2 phosphorylation, thus significantly relieving joint capsule contracture. Our findings indicate the TGFβ/IL11/ERK1/2 axis is an important pathway for the differentiation of fibroblasts into myofibroblasts. Anti-IL11 treatment is an effective means to prevent traumatic joint capsule contracture.

下调 IL-11 可调节 TGFβ/ERK1/2 信号通路,从而抑制关节囊纤维化并缓解创伤后关节囊挛缩。
背景:创伤后关节囊挛缩是关节损伤和手术的常见并发症。创伤后关节囊挛缩与纤维化有关,其特点是肌成纤维细胞过度分化和增殖,细胞外基质异常分泌和积聚。以前的研究表明,IL11 在心肌纤维化中发挥作用。因此,我们推测 IL11 可能在关节囊挛缩过程中起纤维化作用,从而发现预防关节囊挛缩的新靶点 方法:我们通过过度伸展膝关节并将其固定在屈曲位来构建创伤后关节挛缩模型,并在野生型、IL11-/-、IL11R -/-、α-SMA-cre-IL11fl/fl、α-SMA-cre-IL11Rfl/fl小鼠品系中构建创伤后关节囊挛缩模型,以未对膝关节进行任何处理的野生型小鼠为对照组。检测各组小鼠膝关节组织中的纤维化标志物以及 IL11 和 IL11R 的表达。体外分析使用的是 NIH3T3 细胞系。通过 Western 印迹、ELISA 和 RT-qPCR 检测纤维化标志物、IL11、TGFβ 和 ERK1/2 的表达:结果:抑制IL11可抑制ERK1/2磷酸化,减少关节囊胶原蛋白的分泌,抑制创伤后关节囊挛缩中肌成纤维细胞的过度分化和增殖,从而缓解关节囊挛缩,获得更好的关节活动度:结论:在创伤性关节囊挛缩中下调 IL11 可抑制 ERK1/2 磷酸化,从而显著缓解关节囊挛缩。我们的研究结果表明,TGFβ/IL11/ERK1/2 轴是成纤维细胞分化为肌成纤维细胞的重要途径。抗IL11治疗是预防创伤性关节囊挛缩的有效手段。
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来源期刊
CiteScore
6.50
自引率
23.30%
发文量
604
审稿时长
11.2 weeks
期刊介绍: The official publication for eight leading specialty organizations, this authoritative journal is the only publication to focus exclusively on medical, surgical, and physical techniques for treating injury/disease of the upper extremity, including the shoulder girdle, arm, and elbow. Clinically oriented and peer-reviewed, the Journal provides an international forum for the exchange of information on new techniques, instruments, and materials. Journal of Shoulder and Elbow Surgery features vivid photos, professional illustrations, and explicit diagrams that demonstrate surgical approaches and depict implant devices. Topics covered include fractures, dislocations, diseases and injuries of the rotator cuff, imaging techniques, arthritis, arthroscopy, arthroplasty, and rehabilitation.
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