首页> 外文期刊>Osteoarthritis and cartilage >Invivo imaging of MMP-13 activity in the murine destabilised medial meniscus surgical model of osteoarthritis
【24h】

Invivo imaging of MMP-13 activity in the murine destabilised medial meniscus surgical model of osteoarthritis

机译:体内成像MMP-13在鼠稳定的内侧弯月球骨关节炎外科手术模型中的MMP-13活性

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To detect and determine disease severity of osteoarthritis (OA) using a probe activated by matrix metalloproteinase-13 (MMP-13) invivo in the murine destabilised medial meniscus (DMM) surgical model of OA. Design: We have previously described MMP12ap and MMP13ap, internally quenched fluorescent peptide substrate probes that are activated respectively by MMP-12 and MMP-13. Here we used these probes to follow enzyme activity invivo in mice knees 4, 6 and 8 weeks following DMM surgery. After invivo optical imaging, disease severity was determined through traditional histological analysis. The amount of probe activation was analysed for discrimination between DMM, contralateral and sham operated knees, as well as for congruence between activity and histological damage. Results: There was no specific activation of MMP12ap at the time points observed between sham operated and DMM operated, or their respective contralateral joints. The activation of the MMP13ap in the DMM model was highest 6 weeks after surgery, but was only specific compared against sham surgery 8 weeks after surgery (1.5-fold increase). The activation of MMP13ap correlated with histological damage 6 and 8 weeks after surgery, with correlations of 0.484 (P=0.0032) and 0.478 respectively (P=0.0049). This correlation dropped to 0.218 (P=0.011) if all data were considered. Conclusion: The current MMP-13 activity probe is suitable for the discrimination between DMM and sham or contralateral knees 8 weeks after surgery, when cartilage loss is typified by the appearance of small fissures up to the tidemark, but not earlier. This activity correlates with the histological damage observed.
机译:目的:使用鼠标稳定的内膜内半月板(DMM)手术模型中的基质金属蛋白酶-13(MMP-13)Invivo激活的探针检测和确定骨关节炎(OA)的疾病严重程度。设计:我们先前描述了MMP12AP和MMP13AP,内部淬火的荧光肽基底探针分别由MMP-12和MMP-13激活。在这里,我们使用这些探针在DMM手术后6和8周内遵循小鼠膝关节4,6和8周的酶活性invivo。在Invivo光学成像后,通过传统的组织学分析确定疾病严重程度。分析了探针激活的量,用于DMM,对侧和假手动膝盖之间的歧视,以及在活动和组织学损伤之间的一致性。结果:在假手术和DMM操作之间观察到的时间点,或其各自的对侧关节,没有具体激活MMP12AP。在手术后6周的DMM模型中的MMP13AP的激活是最高的,但在手术后8周的假手术比较(1.5倍的增加),才与假手术进行比较。激活MMP13ap与手术后6和8周相关的MMP13ap,分别是0.484(p = 0.0032)和0.478的相关性(P = 0.0049)。如果考虑所有数据,则此相关性降至0.218(p = 0.011)。结论:目前的MMP-13活性探针适用于手术后8周达姆和黑色或对侧膝关节之间的歧视,当软骨损失由小裂隙的出现达到Tidemark,但不是较早。该活动与观察到的组织学损伤相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号