Comparative transcriptomic analysis of articular cartilage of post-traumatic osteoarthritis models

• Published in: Disease models & mechanisms Vol. 17; no. 10
• Main Authors: Gilbert, Sophie J, Soul, Jamie, Hao, Yao, Lin, Hua, Piróg, Katarzyna A, Coxhead, Jonathan, Patel, Krutik, Barter, Matt J, Young, David A, Blain, Emma J
• Format: Journal Article
• Language: English
• Published: England The Company of Biologists Ltd 01-10-2024; The Company of Biologists
• Subjects: acl rupture; Animals; Anterior Cruciate Ligament Injuries - complications; Anterior Cruciate Ligament Injuries - metabolism; Anterior Cruciate Ligament Injuries - pathology; cartilage; Cartilage, Articular - metabolism; Cartilage, Articular - pathology; Chondrocytes - metabolism; Chondrocytes - pathology; Disease Models, Animal; dmm; Gene Expression Profiling; Gene Expression Regulation; Gene Ontology; Humans; Male; Mice; Mice, Inbred C57BL; microrna; MicroRNAs - genetics; MicroRNAs - metabolism; Osteoarthritis - genetics; Osteoarthritis - pathology; ptoa; Transcriptome - genetics; Cartilage; microRNA; PTOA; ACL rupture; DMM
• ISSN: 1754-8403; 1754-8411; 1754-8411
• DOI: 10.1242/dmm.050583

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.