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Matrix Metalloproteinase MMP-9 Promotes K/BxN Serum Induced Arthritis in Mice 被引量:2
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作者 Narendiran Rajasekaran Harald Illges 《Open Journal of Rheumatology and Autoimmune Diseases》 2014年第1期22-28,共7页
Matrix metalloproteinases (MMPs) are matrix-degrading enzymes that are over-expressed in joints of rheumatoid arthritis (RA) patients. However, the contribution of specific MMPs for the development of arthritic joints... Matrix metalloproteinases (MMPs) are matrix-degrading enzymes that are over-expressed in joints of rheumatoid arthritis (RA) patients. However, the contribution of specific MMPs for the development of arthritic joints is unknown. This study is aimed at studying the role of matrix metalloproteinase-9 (MMP-9) in mice, using the K/BxN serum-transfer model of RA. Arthritis was induced in Balb/c mice by injecting K/BxN serum. Development of arthritis was followed in these mice by measuring ankle thickness and clinical index score. MMP-9 expression in the joints of mice killed at various time points during the disease progression was determined by gelatin zymography using ankle lysates. We found that MMP-9 expression increased with the severity of arthritis. Importantly MMP-9 deficient mice injected with K/BxN serum showed a milder form of arthritis in comparison to the control C57BL/6 mice injected with K/BxN serum. We therefore conclude that MMP-9 promotes arthritis in mice. 展开更多
关键词 MMP-9 ANTIBODY INDUCED ARTHRITIS k/bxn GELATIN ZYMOGRAPHY
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Reduced Locomotor Activity Correlates with Increased Severity of Arthritis in a Mouse Model of Antibody-Induced Arthritis
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作者 Narendiran Rajasekaran Ricky Tran +2 位作者 Conrado Pascual Xinmin Xie Elizabeth D. Mellins 《Open Journal of Rheumatology and Autoimmune Diseases》 2014年第1期62-68,共7页
Introduction: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovial hyperplasia and progressive cartilage and bone destruction that leads to a substantial loss of general functions and/or... Introduction: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovial hyperplasia and progressive cartilage and bone destruction that leads to a substantial loss of general functions and/or a decline in physical activities such as walking speed in humans. The K/BxN serum transfer arthritis in mice shares many immunological and pathological features with human RA. Very few studies are available in mice that investigate the changes in physical activity in relation to arthritis development. In this study we investigate the effect of arthritis on the locomotor activity of mice during K/BxN sera transfer arthritis. Methods: Arthritis was induced in Balb/c mice by injecting intraperitoneally with 200 μl of K/BxN sera;Balb/c mice injected with phosphate buffered saline (PBS) served as control. Progress of arthritis was estimated by daily measurements of joint thickness. Each mouse’s locomotor activity (travel distance and travel time) was assessed every day for duration of 20 minute period using the SmartCageTM platform. Data were analyzed using the SmartCageTM analysis software (CageScoreTM). Results: Arthritic Balb/c mice showed a reduction in distance covered and travel speed when compared to arthritis-free, control Balb/c mice. Maximum decline in locomotor activity was observed during the peak period of the disease and correlated to the increase in joint thickness in the arthritic mice. Conclusion: This report demonstrates that measuring locomotor activity of mice during progression of K/BxN sera-induced arthritis using the SmartCageTM platform offers a quantitative method to assess physical activity in mice during arthritis. 展开更多
关键词 k/bxn ARTHRITIS Locomotion SERUM Transfer
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LTB4和BLT1在类风湿关节炎中的作用 被引量:3
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作者 魏志萍 《中国医药科学》 2020年第12期50-52,共3页
类风湿关节炎是一种慢性的、系统性的、以关节滑膜炎为主要特征的自身免疫疾病,发病机制尚未完全明确,是临床难以治愈的疾病之一。白三烯B4(LTB4)是一种炎症脂质介体,其受体有两类分别为BLT1和BLT2。LTB4与BLT1亲和力较高,研究表明LTB4... 类风湿关节炎是一种慢性的、系统性的、以关节滑膜炎为主要特征的自身免疫疾病,发病机制尚未完全明确,是临床难以治愈的疾病之一。白三烯B4(LTB4)是一种炎症脂质介体,其受体有两类分别为BLT1和BLT2。LTB4与BLT1亲和力较高,研究表明LTB4和BLT1在小鼠类风湿关节炎发病机制中具有非常关键的作用,因此探索LTB4-BLT1途径在关节炎发病中的作用及机制,可为关节炎的临床治疗提供新的方向,本文对LTB4和BLT1在类风湿关节炎的作用进行综述。 展开更多
关键词 类风湿关节炎 LTB4 BLT1 型胶原诱导的关节炎动物模型 k/bxn血清转移性关节炎小鼠模型
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动脉粥样硬化合并血清诱导型炎性关节炎小鼠肠道菌群和免疫系统的变化
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作者 石娜 张抒扬 牛海涛 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2019年第4期283-291,共9页
目的探讨动脉粥样硬化(动脉硬化)合并血清诱导型炎性关节炎小鼠肠道菌群及免疫系统的变化。方法实验分为ApoE基因缺陷(ApoE^-/-)组和C57BL/6对照组,通过给8周龄ApoE^-/-小鼠和C57BL/6小鼠分别饲喂高脂食物,ELISA法检测血脂蛋白水平,油红... 目的探讨动脉粥样硬化(动脉硬化)合并血清诱导型炎性关节炎小鼠肠道菌群及免疫系统的变化。方法实验分为ApoE基因缺陷(ApoE^-/-)组和C57BL/6对照组,通过给8周龄ApoE^-/-小鼠和C57BL/6小鼠分别饲喂高脂食物,ELISA法检测血脂蛋白水平,油红O染色来评价动脉硬化斑块面积,从而评估小鼠患动脉硬化的严重程度。从17周龄起腹腔注射K/BxN血清至26周龄,游标卡尺测量小鼠踝关节宽度,通过踝关节宽度和血清诱导型炎性关节炎评分来评价小鼠患血清诱导型炎性关节炎的程度。取小鼠粪便并提取DNA进行16S V4区PCR扩增,Illumina HiSeq PE250上机测序。分离小鼠脾脏细胞和骨髓细胞并用流式抗体染色,经流式细胞仪分析免疫细胞分布的改变。结果与C57BL/6对照组相比,动脉硬化合并血清诱导型炎性关节炎小鼠血脂水平显著升高,动脉硬化斑块面积显著增加;踝关节宽度和血清诱导型炎性关节炎评分降低;肠道菌群多样性降低,疣微菌纲显著降低;脾脏和骨髓CD3^+T细胞和CD19^+B细胞显著降低,CD11b^+巨噬细胞显著升高。结论动脉硬化合并血清诱导型炎性关节炎引起小鼠免疫细胞分布改变,肠道菌群多样性降低,细菌菌群分布改变,健康肠道的潜在生物标志物艾克曼菌丰度降低。推测肠道微生物的改变可能参与动脉硬化合并血清诱导型炎性关节炎的发病机制。 展开更多
关键词 动脉硬化 血清诱导型炎性关节炎 肠道微生物 自身免疫
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