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作 者:余晓明[1] 袁雪凌[1] 孟昊业[1] 孙振[1] 尹合勇 郭全义[1] 彭江[1] 汪爱媛[1] 卢世璧[1]
机构地区:[1]解放军总医院骨科研究所,北京100853 [2]南开大学,天津300071
出 处:《解放军医学院学报》2015年第11期1131-1133,共3页Academic Journal of Chinese PLA Medical School
基 金:国家"863"计划项目(2012AA020502);全军十二五重点项目(BWS11J025);国家"973"重点基础研究发展规划项目(2012CB518106)~~
摘 要:目的探讨不同Kellgren-Lawrence X线分级的骨性关节炎患者膝关节软骨及软骨下骨中Micro RNA-214(mi R-214)的表达,为进一步研究mi R-214在骨性关节炎发生和发展中的作用提供依据。方法收集截肢患者及骨性关节炎全膝关节置换患者膝关节胫骨平台40例,根据K-L评分标准将其分为Ⅰ级组(10例)、Ⅱ级组(10例)、Ⅲ级组(10例)、Ⅳ级组(10例)。将样本进行软骨及软骨下骨分离后,运用实时定量PCR检测不同分组中软骨及软骨下骨中mi R-214的表达情况。结果在所有软骨及软骨下骨中均能检测到mi R-214的表达。比较4组之间mi R-214的表达情况,发现4组软骨中mi R-214的表达有明显差异(P<0.05),并且呈现逐渐升高的趋势;骨性关节炎发展的严重程度与mi R-214的表达水平密切相关。Ⅲ级组中软骨下骨中的mi R-214的表达量明显高于其他3组(P<0.05)。结论 mi R-214的表达水平与骨性关节炎发展的严重程度密切相关,表明mi R-214可能与骨性关节炎的发生、发展有密切联系。Objective To detect the expression level of micro RNA-214(mi R-214) in cartilage and subchondral bone of different graded osteoarthritis(OA), which was classified by X-ray diagnosis criteria of Kellgren and Lawrence, and provide theoretical foundation for researching the role of mi R-214 in OA development. Methods Tibial plateaus of OA patients were collected from those who underwent total knee arthroplasty(TKA) and amputation. Forty samples were divided into 4 groups by K-L osteoarthritis scoring system: gradeⅠgroup(n=10), gradeⅡgroup(n=10), gradeⅢgroup(n=10), and gradeⅣgroup(n=10). After getting the samples, we segregated cartilage and subchondral bone, and the expression level of mi R-214 by real-time PCR was tested. Resultsmi R-214 was examined in all cartilage and subchondral bone. The expression level of mi R-214 was compared in four groups, and it showed a rising trend with significant difference(P〈0.05). Positive correlation was found between the severity of OA and the expression level of mi R-214. Among the four groups, the level of mi R-214 in subchondral bone was highest. Conclusion The expression level of mi R-214 in 4 groups is keeping rising, which is related to the severity of OA progression. And the expression level of mi R-214 also has obvious change in subchondral bone. Our findings indicate that mi R-214 has intertwined relationshiP〈0with the development and progression of OA, which provides theoretical foundation for OA development and treatment.
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