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Title: Widespread Epigenomic, Transcriptomic and Proteomic Differences Between Hip Osteophytic and Articular Patient Chondrocytes in Osteoarthritis
Authors: Steinberg J; Brooks RA; Southam L; Bhatnagar S; Roumeliotis TI; Hatzikotoulas K; Zengini E; Wilkinson JM; Choudhary JS; McCaskie AW; Zeggini E
Year: 2018
Journal Title: Rheumatology
Volume: 57
Issue: 8
Page number start: 1481
Page number end: 1489
Abstract: Objectives. To identify molecular differences between chondrocytes from osteophytic and articular cartilage tissue from OA patients. Methods. We investigated genes and pathways by combining genome-wide DNA methylation, RNA sequencing and quantitative proteomics in isolated primary chondrocytes from the cartilaginous layer of osteophytes and matched areas of low- and high-grade articular cartilage across nine patients with OA undergoing hip replacement surgery. Results. Chondrocytes from osteophytic cartilage showed widespread differences to low-grade articular cartilage chondrocytes. These differences were similar to, but more pronounced than, differences between chondrocytes from osteophytic and high-grade articular cartilage, and more pronounced than differences between high- and low-grade articular cartilage. We identified 56 genes with significant differences between osteophytic chondrocytes and low-grade articular cartilage chondrocytes on all three omics levels. Several of these genes have known roles in OA, including ALDH1A2 and cartilage oligomeric matrix protein, which have functional genetic variants associated with OA from genome-wide association studies. An integrative gene ontology enrichment analysis showed that differences between osteophytic and low-grade articular cartilage chondrocytes are associated with extracellular matrix organization, skeletal system development, platelet aggregation and regulation of ERK1 and ERK2 cascade. Conclusion. We present a first comprehensive view of the molecular landscape of chondrocytes from osteophytic cartilage as compared with articular cartilage chondrocytes from the same joints in OA. We found robust changes at genes relevant to chondrocyte function, providing insight into biological processes involved in osteophyte development and thus OA progression.
Division: Cancer Research Division
DOI: 10.1093/rheumatology/key101
Appears in Collections:Research Articles

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