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Effect of small interference RNA (siRNA) for ADAMTS5 on intervertebral disc degeneration in the rabbit anular needle-puncture model

机译:ADAMTS5小干扰RNA(siRNA)对兔肛门穿刺模型椎间盘退变的影响

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Introduction The etiology of degenerative disc disease is unknown. Several investigators have reported the presence of proteolytic enzymes, such as the matrix metalloproteinase (MMP) and ADAMTS (a disintegrin and metalloprotease with thrombospondin-like repeats) families, in degenerated human discs. Glasson and colleagues recently reported that a significant reduction occurs in the severity of cartilage destruction in ADAMTS5 knockout mice compared with wild-type mice. The purpose of this study was to evaluate the suppressive effects of injections of ADAMTS5 small interference RNA (siRNA) oligonucleotide on intervertebral disc degeneration in the rabbit anular needle-puncture model. Methods Rabbit nucleus pulposus (NP) cells were transfected with siRNA oligonucleotides specific for ADAMTS5 or the control. The suppression of the ADAMTS5 gene by siRNA transfection was assessed by using real-time polymerase chain reaction (PCR), both in monolayer and alginate bead cultures with or without interleukin-1β (IL-1β) stimulation. The effect of siRNA was determined in vivo by using the rabbit anular needle-puncture model (control group: n = 8; ADAMTS5 group: n = 8). One week after the initial anular puncture, the animals received an injection of the control or anti- ADAMTS5 oligonucleotide (100 μg each at the L2/3 and L4/5 level; 16 discs/group). Disc height, magnetic resonance imaging (MRI) (Thompson classification and signal intensity), and safranin-O staining (histologic grade) were assessed. Results IL-1β treatment significantly increased the ADAMTS5 mRNA level in NP cells ( P < 0.01). ADAMTS5 gene suppression was 70% compared with the control oligonucleotide in both monolayer and alginate bead culture with or without stimulation with IL-1β. The injection of anti- ADAMTS5 oligonucleotide in vivo resulted in improved MRI scores with increased signal intensity and improved histologic grade scores with statistical significance ( P < 0.05). No significant change in disc height was observed. Conclusions A single injection of ADAMTS5 siRNA induced the suppression of degradation in NP tissues, as shown by significantly improved MRI and histologic grades. The mechanism of response to siRNA may be worthy of exploration for possible therapeutic purposes.
机译:简介变性椎间盘疾病的病因尚不清楚。几位研究者报告说,变性的人椎间盘中存在蛋白水解酶,例如基质金属蛋白酶(MMP)和ADAMTS(具有血小板反应蛋白样重复序列的双整合素和金属蛋白酶)家族。 Glasson及其同事最近报道,与野生型小鼠相比,ADAMTS5基因敲除小鼠的软骨破坏严重程度显着降低。这项研究的目的是评估注射ADAMTS5小干扰RNA(siRNA)寡核苷酸对兔肛门穿刺模型中椎间盘退变的抑制作用。方法用对ADAMTS5或对照特异的siRNA寡核苷酸转染兔髓核(NP)细胞。 siRNA转染对ADAMTS5基因的抑制作用是通过使用实时聚合酶链反应(PCR)在有或没有白介素1β(IL-1β)刺激的单层和藻酸盐珠培养物中进行评估的。 siRNA的作用是通过使用兔子肛门穿刺模型在体内确定的(对照组:n = 8; ADAMTS5组:n = 8)。首次穿刺后一周,动物接受了对照或抗ADAMTS5寡核苷酸注射(L2 / 3和L4 / 5水平各100μg; 16个椎间盘/组)。评估椎间盘高度,磁共振成像(MRI)(汤普森分类和信号强度)和番红O染色(组织学等级)。结果IL-1β处理显着增加了NP细胞中ADAMTS5 mRNA的水平(P <0.01)。在有或没有IL-1β刺激的单层和藻酸盐珠培养物中,与对照寡核苷酸相比,ADAMTS5基因抑制率为70%。体内注射抗ADAMTS5寡核苷酸可提高MRI评分,增强信号强度,并改善组织学评分,具有统计学意义(P <0.05)。观察到椎间盘高度没有明显变化。结论一次注射ADAMTS5 siRNA可抑制NP组织的降解,如MRI和组织学评分明显改善所表明。对于siRNA的应答机制可能值得探索用于可能的治疗目的。

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