Department of Veterinary Clinical Sciences, The Ohio State University, Columbus, OH, USA.
Osteoarthritis Cartilage. 2012 Dec;20(12):1610-8. doi: 10.1016/j.joca.2012.08.011. Epub 2012 Aug 27.
Diminish interleukin-1β (IL-1β) signaling in a model of primary osteoarthritis by RNA interference-based transcript reduction or receptor blockade, and quantify changes incurred on transcript expression of additional mediators.
Knees of Hartley guinea pigs were collected at 120 and 180 days of age following injection with viral vectors (N = 4/treatment group/date) at 60 days. Two groups received either adeno-associated viral serotype 5 vector containing a knockdown sequence (TV), or adenoviral vector encoding for IL-1 receptor antagonist protein (Ad-IRAP); treatments were contrasted with opposite knees administered corresponding vector controls. A third group evaluated TV relative to saline-only injected knees. Chondropathy and immunohistochemistry findings were compared to untreated guinea pigs. Transcript expression levels in cartilage were calculated using the comparative CT (2(-ΔΔCT)) method and analyzed by one-way analysis of variance (ANOVA) with pairwise comparisons using Tukey 95% confidence intervals.
Vector transduction was confirmed at both harvest dates. TV and Ad-IRAP, relative to vector controls, significantly decreased IL-1β. Inflammatory mediators [tumor necrosis factor-α (TNF-α), IL-8, interferon-γ (IFN-γ)], and catabolic matrix metalloproteinase 13 (MMP13) were also decreased, while anabolic transforming growth factor-β1 (TGF-β1) was increased. IL-1β was also decreased by TV vs saline, with a decrease in MMP13 and increase TGF-β1; TNF-α, IL-8, and IFN-γ were transiently increased.
This work confirmed that a reduction in IL-1β signaling was accomplished by either method, resulting in decreased expression of three inflammatory mediators and one catabolic agent, and increased expression of an anabolic molecule. Thus, evidence is provided that IL-1β serves a role in vivo in spontaneous osteoarthritis and that these translational tools may provide beneficial disease modification.
通过 RNA 干扰转录减少或受体阻断,减少原发性骨关节炎模型中的白细胞介素-1β(IL-1β)信号,并定量分析其他介质的转录表达变化。
在 60 天时向 120 天和 180 天龄的 Hartley 豚鼠膝关节中注射病毒载体(每组/日 N=4)后收集膝关节。两组分别接受携带下调序列的腺相关病毒血清型 5 载体(TV)或编码白细胞介素 1 受体拮抗剂蛋白的腺病毒载体(Ad-IRAP)治疗;将治疗结果与相反膝关节接受相应载体对照进行对比。第三组评估 TV 与仅生理盐水注射膝关节的相对关系。比较软骨病变和免疫组织化学发现与未处理的豚鼠进行比较。采用比较 CT(2(-ΔΔCT))方法计算软骨中的转录表达水平,并采用单因素方差分析(ANOVA)进行分析,使用 Tukey 95%置信区间进行两两比较。
在两个收获日期均证实了载体转导。TV 和 Ad-IRAP 与载体对照相比,显著降低了 IL-1β。炎症介质[肿瘤坏死因子-α(TNF-α)、白细胞介素-8(IL-8)、干扰素-γ(IFN-γ)]和分解代谢基质金属蛋白酶 13(MMP13)也减少,而合成代谢转化生长因子-β1(TGF-β1)增加。与盐水相比,TV 也降低了 IL-1β,同时降低了 MMP13 并增加了 TGF-β1;TNF-α、IL-8 和 IFN-γ短暂增加。
这项工作证实,通过两种方法均可实现 IL-1β 信号的减少,导致三种炎症介质和一种分解代谢因子的表达减少,以及一种合成代谢分子的表达增加。因此,有证据表明 IL-1β 在自发性骨关节炎的体内发挥作用,并且这些转化工具可能提供有益的疾病修饰。