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首页> 外文期刊>Upsala journal of medical sciences >Expression of transforming growth factor-β1 and connective tissue growth factor in the capsule in a rat immobilized knee model
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Expression of transforming growth factor-β1 and connective tissue growth factor in the capsule in a rat immobilized knee model

机译:大鼠固定膝模型中转化生长因子-β1和结缔组织生长因子在胶囊中的表达

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Background : Contracture is a very common complication of joint immobilization in daily examination, but its cause is still unknown. A fibrotic change of the capsule is suggested to be one of the main causes of the joint contracture. The goal of this study was to analyze the expression pattern of transforming growth factor-β1 (TGF-β1) and connective tissue growth factor (CTGF), which are implicated in fibrosis in the capsule of a rat immobilized knee model. Materials and Methods : We immobilized the unilateral knee joints of 66 rats in 150 degrees of flexion using a plastic plate and metal screws. Sham operated knee joints of 66 rats had holes drilled and screws inserted but none of them were plated. The capsule from the anterior and posterior portion of the knee joints was harvested at 3 days, 1, 2, 4, 8 and 16 weeks after immobilization and the expression patterns of TGF-β1 and CTGF were characterized using in situ hybridization and immunohistochemistry. Results : The in situ hybridization demonstrated that the mRNAs of both TGF-β1 and CTGF increased continuously during the first 2 weeks after immobilization and then decreased. The response was relatively higher in the posterior capsule than in the anterior one. In contrast, the immunoreactivity of both TGF-β1 and CTGF increased gradually with time. The response was much stronger in the posterior capsule than in the anterior one. Conclusions : The capsule has a potency to produce TGF-β1 and CTGF after immobilization. CTGF may play a role in causing and maintaining capsular fibrosis in collaboration with TGF-β1. The fibrotic change in the posterior capsule may have resulted in limited motion in extension in this immobilized knee model in rats. It may be possible to prevent joint contractures by somehow blocking the fibrotic process.
机译:背景:挛缩症是日常检查中关节固定的一种非常常见的并发症,但其原因尚不清楚。胶囊的纤维化改变被认为是关节挛缩的主要原因之一。这项研究的目的是分析转化生长因子-β1(TGF-β1)和结缔组织生长因子(CTGF)的表达模式,这与大鼠固定膝关节模型的胶囊中的纤维化有关。材料和方法:我们使用塑料板和金属螺钉将150只屈曲度的66只大鼠的单侧膝关节固定。假手术的66只大鼠的膝关节上钻了孔,并插入了螺钉,但均未电镀。固定后第3、1、2、4、8和16周收集膝关节前后部的包膜,并通过原位杂交和免疫组织化学表征TGF-β1和CTGF的表达模式。结果:原位杂交表明,TGF-β1和CTGF的mRNA在固定后的前2周均持续升高,然后下降。后囊的反应相对高于前囊。相反,TGF-β1和CTGF的免疫反应性均随时间逐渐增加。后囊的反应比前囊的反应强得多。结论:该胶囊固定后具有产生TGF-β1和CTGF的潜能。 CTGF可能与TGF-β1协同作用导致并维持包膜纤维化。后囊中的纤维化变化可能导致这种固定的膝关节模型大鼠伸展运动受限。有可能通过某种方式阻止纤维化过程来预防关节挛缩。

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