Biomechanics and Bioengineering Research Centre Versus Arthritis, Biomedicine Division, School of Biosciences, The Sir Martin Evans Building, Cardiff University, Cardiff CF10 3AX, Wales, UK.
Biosciences Institute, Newcastle University, Centre for Life, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK.
Dis Model Mech. 2024 Oct 1;17(10). doi: 10.1242/dmm.050583. Epub 2024 Oct 21.
Animal models of post-traumatic osteoarthritis (PTOA) recapitulate the pathological changes observed in human PTOA. Here, skeletally mature C57Bl6 mice were subjected to either rapid-onset non-surgical mechanical rupture of the anterior cruciate ligament (ACL) or to surgical destabilisation of the medial meniscus (DMM). Transcriptome profiling of micro-dissected cartilage at day 7 or day 42 following ACL or DMM procedure, respectively, showed that the two models were comparable and highly correlative. Gene ontology (GO) enrichment analysis identified similarly enriched pathways that were overrepresented by anabolic terms. To address the transcriptome changes more completely in the ACL model, we also performed small RNA sequencing, describing the first microRNA profile of this model. miR-199-5p was amongst the most abundant, yet differentially expressed, microRNAs, and its inhibition in primary human chondrocytes led to a transcriptome response that was comparable to that observed in both human 'OA damaged vs intact cartilage' and murine DMM cartilage datasets. We also experimentally verified CELSR1, GIT1, ECE1 and SOS2 as novel miR-199-5p targets. Together, these data support the use of the ACL rupture model as a non-invasive companion to the DMM model.
动物创伤后骨关节炎(PTOA)模型再现了人类 PTOA 中观察到的病理变化。在这里,成熟的 C57Bl6 小鼠分别接受快速发作的非手术机械性前交叉韧带(ACL)断裂或内侧半月板(DMM)手术不稳定的处理。分别在 ACL 或 DMM 手术后 7 天或 42 天对微解剖软骨进行转录组分析,结果表明这两种模型具有可比性且高度相关。基因本体(GO)富集分析确定了类似的富集途径,这些途径由合成代谢术语过度表示。为了更全面地研究 ACL 模型中的转录组变化,我们还进行了小 RNA 测序,描述了该模型的第一个 microRNA 图谱。miR-199-5p 是最丰富但差异表达的 microRNAs 之一,其在原代人软骨细胞中的抑制作用导致的转录组反应与在人类“OA 损伤 vs 完整软骨”和鼠 DMM 软骨数据集中观察到的反应相似。我们还通过实验验证了 CELSR1、GIT1、ECE1 和 SOS2 是新型 miR-199-5p 的靶标。这些数据共同支持将 ACL 断裂模型用作 DMM 模型的非侵入性伴侣。