Kourtis Aristotelis, Adamopoulos Panagiotis G, Papalois Apostolos, Iliopoulos Dimitrios C, Babis George C, Scorilas Andreas
Athens Medical Centre, Athens, Greece.
Department of Biochemistry and Molecular Biology, National and Kapodistrian University of Athens, Athens, Greece.
Ann Transl Med. 2018 Jun;6(12):243. doi: 10.21037/atm.2018.05.47.
Given that apoptosis of chondrocytes is one of the most important factors related to the pathogenesis of osteoarthritis (OA), the recent research interest adds progress not only to the knowledge of the molecular signals that mediate apoptosis but also to find new therapeutic targets. This study attempts to investigate the differential expression of family genes in the articular cartilage of an experimental animal model of OA.
In total, 26 New Zealand white rabbits underwent an anterior cruciate ligament transaction, 26 more were subjected to a placebo surgery and 18 specimens constituted the control non-operated group. Thirteen weeks later, samples of cartilage from the osteoarthritic and non-osteoarthritic knees were collected and subjected to analysis of the , and gene expression at the mRNA level.
Installed osteoarthritic alterations of varied intensity and of grade 1 up to grade 5, were confirmed according to the OARSI system. Contrary to the physiologically healthy samples, in the osteoarthritic samples the mRNA expression levels of and genes were found significantly upregulated by signals which can activate apoptosis. However, the difference between mRNA expression levels in healthy and osteoarthritic samples was not supported statistically.
Since apoptosis is the main feature of the cartilage degeneration in OA, the effective inhibition of apoptosis of chondrocytes can provide novel and interesting therapeutic strategies for the treatment of OA. Therefore, and are highlighted as potential therapeutic targets in OA.
鉴于软骨细胞凋亡是与骨关节炎(OA)发病机制相关的最重要因素之一,最近的研究兴趣不仅在介导凋亡的分子信号知识方面取得了进展,还在于寻找新的治疗靶点。本研究试图调查OA实验动物模型关节软骨中家族基因的差异表达。
总共26只新西兰白兔接受了前交叉韧带切断术,另外26只接受了安慰剂手术,18个标本构成未手术的对照组。13周后,收集骨关节炎和非骨关节炎膝关节的软骨样本,并对基因在mRNA水平的表达进行分析。
根据OARSI系统,证实存在强度不同、1级至5级的骨关节炎改变。与生理健康样本相反,在骨关节炎样本中,发现基因和基因的mRNA表达水平被可激活凋亡的信号显著上调。然而,健康样本和骨关节炎样本中基因mRNA表达水平的差异在统计学上未得到支持。
由于凋亡是OA软骨退变的主要特征,有效抑制软骨细胞凋亡可为OA治疗提供新的有趣的治疗策略。因此,和被突出显示为OA潜在的治疗靶点。