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缺氧介导的细胞焦亡在大鼠膝关节伸直挛缩发展中的作用。

Role of hypoxia-mediated pyroptosis in the development of extending knee joint contracture in rats.

机构信息

Department of Rehabilitation Medicine, The Second Affiliated Hospital of Anhui Medical University, No.678 Furong Road, Economic and Technological Development Zone, Hefei, 230601, Anhui, China.

Hefei Institute of Physical Sciences, Chinese Academy of Sciences, Hefei, 230031, Anhui, China.

出版信息

Eur J Med Res. 2024 May 27;29(1):298. doi: 10.1186/s40001-024-01890-9.

Abstract

Joint contracture is one of the common diseases clinically, and joint capsule fibrosis is considered to be one of the most important pathological changes of joint contracture. However, the underlying mechanism of joint capsule fibrosis is still controversial. The present study aims to establish an animal model of knee extending joint contracture in rats, and to investigate the role of hypoxia-mediated pyroptosis in the progression of joint contracture using this animal model. 36 male SD rats were selected, 6 of which were not immobilized and were used as control group, while 30 rats were divided into I-1 group (immobilized for 1 week following 7 weeks of free movement), I-2 group (immobilized for 2 weeks following 6 weeks of free movement), I-4 group (immobilized for 4 weeks following 4 weeks of free movement), I-6 group (immobilized for 6 weeks following 2 weeks of free movement) and I-8 group (immobilized for 8 weeks) according to different immobilizing time. The progression of joint contracture was assessed by the measurement of knee joint range of motion, collagen deposition in joint capsule was examined with Masson staining, protein expression levels of HIF-1α, NLRP3, Caspase-1, GSDMD-N, TGF-β1, α-SMA and p-Smad3 in joint capsule were assessed using western blotting, and the morphological changes of fibroblasts were observed by transmission electron microscopy. The degree of total and arthrogenic contracture progressed from the first week and lasted until the first eight weeks after immobilization. The degree of total and arthrogenic contracture progressed rapidly in the first four weeks after immobilization and then progressed slowly. Masson staining indicated that collagen deposition in joint capsule gradually increased in the first 8 weeks following immobilization. Western blotting analysis showed that the protein levels of HIF-1α continued to increase during the first 8 weeks of immobilization, and the protein levels of pyroptosis-related proteins NLRP3, Caspase-1, GSDMD-N continued to increase in the first 4 weeks after immobilization and then decreased. The protein levels of fibrosis-related proteins TGF-β1, p-Smad3 and α-SMA continued to increase in the first 8 weeks after immobilization. Transmission electron microscopy showed that 4 weeks of immobilization induced cell membrane rupture and cell contents overflow, which further indicated the activation of pyroptosis. Knee extending joint contracture animal model can be established by external immobilization orthosis in rats, and the activation of hypoxia-mediated pyroptosis may play a stimulating role in the process of joint capsule fibrosis and joint contracture.

摘要

关节挛缩是临床上常见的疾病之一,关节囊纤维化被认为是关节挛缩的最重要的病理变化之一。然而,关节囊纤维化的潜在机制仍存在争议。本研究旨在建立一种大鼠膝关节伸直挛缩的动物模型,并利用该动物模型探讨缺氧介导的焦亡在关节挛缩进展中的作用。选择 36 只雄性 SD 大鼠,其中 6 只不固定,作为对照组,其余 30 只大鼠根据不同的固定时间分为 I-1 组(固定 1 周后自由活动 7 周)、I-2 组(固定 2 周后自由活动 6 周)、I-4 组(固定 4 周后自由活动 4 周)、I-6 组(固定 2 周后自由活动 2 周)和 I-8 组(固定 8 周)。通过测量膝关节活动范围评估关节挛缩的进展,采用 Masson 染色观察关节囊胶原沉积,采用 Western blot 检测关节囊中 HIF-1α、NLRP3、Caspase-1、GSDMD-N、TGF-β1、α-SMA 和 p-Smad3 的蛋白表达水平,透射电镜观察成纤维细胞的形态变化。结果显示,总挛缩和关节挛缩的程度从固定后的第一周开始进展,并持续到固定后的第八周。固定后前四周总挛缩和关节挛缩进展迅速,然后进展缓慢。Masson 染色显示,固定后 8 周内关节囊胶原沉积逐渐增加。Western blot 分析显示,固定后 8 周内 HIF-1α 蛋白水平持续升高,固定后前 4 周焦亡相关蛋白 NLRP3、Caspase-1、GSDMD-N 蛋白水平持续升高,然后降低。固定后 8 周 TGF-β1、p-Smad3 和 α-SMA 蛋白水平持续升高。透射电镜显示,4 周固定可导致细胞膜破裂和细胞内容物溢出,进一步提示焦亡的激活。结论:通过大鼠外固定矫形器可建立膝关节伸展挛缩动物模型,缺氧介导的焦亡的激活可能在关节囊纤维化和关节挛缩过程中起刺激作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c33/11129407/23ca83884ed5/40001_2024_1890_Fig1_HTML.jpg

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