骨性关节炎患者膝关节软骨及软骨下骨中miR-214的表达

Expression level of miR-214 in cartilage and subchondral bone of patients with osteoarthritis

  • 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MicroRNA-214(miR-214)的表达,为进一步研究miR-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miR-214的表达情况。 结果 在所有软骨及软骨下骨中均能检测到miR-214的表达。比较4组之间miR-214的表达情况,发现4组软骨中miR-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miR-214的表达水平密切相关。Ⅲ级组中软骨下骨中的miR-214的表达量明显高于其他3组(P< 0.05)。 结论 miR-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miR-214可能与骨性关节炎的发生、发展有密切联系。

     

    Abstract: Objective To detect the expression level of microRNA-214 (miR-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 miR-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 miR-214 by real-time PCR was tested. Results miR-214 was examined in all cartilage and subchondral bone. The expression level of miR-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 miR-214. Among the four groups, the level of miR-214 in subchondral bone was highest. Conclusion The expression level of miR-214 in 4 groups is keeping rising, which is related to the severity of OA progression. And the expression level of miR-214 also has obvious change in subchondral bone. Our findings indicate that miR-214 has intertwined relationship with the development and progression of OA, which provides theoretical foundation for OA development and treatment.

     

/

返回文章
返回