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Local intra-articular injection of rapamycin inhibits NLRP3 activity and prevents osteoarthritis in mouse DMM models.
Autoimmunity ( IF 3.3 ) Pub Date : 2019-08-13 , DOI: 10.1080/08916934.2019.1643844
Gang Xu 1 , Jian Wang 1 , Long Ma 1, 2 , Xin Zhao 1, 2 , Wen Luo 1 , Qunhua Jin 1, 2
Affiliation  

This study investigated the influence of autophagy on the expression of Collagen type II and light chain 3 (LC-3) in the articular cartilage of osteoarthritis (OA) models. The expression of OA associated biomarkers namely Matrix metalloproteinase (MMP-13), NOD-, LRR- and pyrin domain-containing 3 (NLRP3) induced by destabilizing the medial meniscus operation (DMM) were also investigated. A total of 60 C57BL/6 mice were divided into (1) control; (2) DMM2; (3) DMM8; (4) rapamycin 2 weeks; and (5) rapamycin 8 weeks groups. Saffranin O-Fast green staining, histomorphometry and immunohistochemical methods were used for analysis. In the DMM group, the expression of the OA biomarkers MMP-13, NLRP3 significantly increased, whilst Collagen II and LC-3B levels were significantly lower than other experimental groups. We hypothesized that NLRP3 inhibits autophagy activation and delays disease progression.

中文翻译:

在小鼠DMM模型中,局部关节内注射雷帕霉素可抑制NLRP3活性并预防骨关节炎。

这项研究调查了自噬对骨关节炎(OA)模型的II型胶原和轻链3(LC-3)表达的影响。还研究了通过破坏内侧半月板操作(DMM)诱导的与OA相关的生物标志物,即基质金属蛋白酶(MMP-13),NOD,LRR和含吡啶结构域的3(NLRP3)的表达。总共60只C57BL / 6小鼠被分为(1)对照。(2)DMM2;(3)DMM8;(4)雷帕霉素2周;(5)雷帕霉素8周组。番红花O-快速绿色染色,组织形态测定法和免疫组化方法用于分析。在DMM组中,OA生物标志物MMP-13,NLRP3的表达显着增加,而II型胶原和LC-3B的水平则明显低于其他实验组。
更新日期:2019-11-01
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