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Characterization of pro-apoptotic and matrix-degradative gene expression following induction of osteoarthritis in mature and aged rabbits.

机译:诱导成熟和老年兔骨关节炎后促凋亡和基质降解基因表达的特征。

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OBJECTIVE: The genetic and molecular changes leading to the distinctive alterations of aged cartilage and its propensity for developing osteoarthritis (OA) are unknown. We hypothesized that pro-apoptotic and matrix-degradative gene expression in a rabbit model of induced OA using mature and aged animals might elucidate this relationship. METHODS: Groups of six mature and aged rabbits underwent anterior cruciate ligament transection (ACLT) and were sacrificed 4 weeks after surgery to create an Outerbridge grade II OA. RNA was extracted from the articular cartilage and menisci of the affected knee and was examined with regard to expression of the following genes: Caspase 8, Fas, Fas ligand (Fas-L), p53, aggrecanase, matrix metalloproteinase (MMP)-1, and MMP-3-MMP-13. A second cohort of mature and aged animals was sacrificed with no intervention to the joint and gene expression was assessed in a similar manner. RESULTS: Fas and Caspase 8 showed significantly increased expression in the cartilage of mature animals with induced OA when compared to unoperated controls while induction of OA in aged rabbits did not significantly increase expression of any of the apoptosis genes. Among unoperated animals, the aged cohort showed significantly increased expression of MMP-1 and aggrecanase in cartilage when compared to mature animals. MMP-13 expression was upregulated in aged cartilage following induction of OA. Although ACLT animals showed gross thinning and irregularities within the meniscus, only the expression of Caspase 8 in the aged rabbits was significantly increased after induction of OA. CONCLUSIONS: Aging of articular cartilage shares some qualities with the development of OA, as seen in the parallel increases in gene expression of Caspase 8 and Fas. Although this may imply a common mechanism of cartilage degeneration in aging and OA or even a spectrum of disease, both are complex processes requiring further study.
机译:目的:遗传和分子变化导致老年软骨的独特改变及其发展为骨关节炎(OA)的倾向尚不清楚。我们假设在使用成熟和老年动物诱发的OA兔模型中促凋亡和基质降解的基因表达可能阐明了这种关系。方法:每组六只成年和成年兔子进行前交叉韧带横断术(ACLT),并在术后4周处死,以创建Outerbridge II级OA。从患膝关节软骨和半月板中提取RNA,并检查以下基因的表达:半胱天冬酶8,Fas,Fas配体(Fas-L),p53,聚集蛋白聚糖酶,基质金属蛋白酶(MMP)-1,和MMP-3-MMP-13。在不干预关节的情况下处死第二批成年和成年动物,并以类似方式评估基因表达。结果:与未手术的对照组相比,Fas和Caspase 8在诱导OA的成熟动物的软骨中表达显着增加,而在老年兔中诱导OA并未显着增加任何凋亡基因的表达。在未手术的动物中,与成熟的动物相比,老年组的软骨中MMP-1和软骨聚集蛋白聚糖酶的表达显着增加。诱导OA后,老年软骨中MMP-13表达上调。尽管ACLT动物在半月板内显示出明显的变薄和不规则性,但是在诱导OA后,仅Caspase 8在老年兔子中的表达显着增加。结论:软骨的老化与OA的发展有一些共同之处,如Caspase 8和Fas基因表达的平行增加所见。尽管这可能暗示了衰老和OA甚至一系列疾病中软骨退变的常见机制,但两者都是复杂的过程,需要进一步研究。

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