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Gene expression changes in damaged osteoarthritic cartilage identify a signature of non-chondrogenic and mechanical responses.
Dunn, S L; Soul, J; Anand, S; Schwartz, J-M; Boot-Handford, R P; Hardingham, T E.
Affiliation
  • Dunn SL; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, UK. Electronic address: sara.dunn@manchester.ac.uk.
  • Soul J; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, UK. Electronic address: jamie.soul@postgrad.manchester.ac.uk.
  • Anand S; Stockport NHS Foundation Trust, Manchester, UK. Electronic address: sanjayanand@doctors.org.uk.
  • Schwartz JM; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, UK. Electronic address: jean-marc.Schwartz@manchester.ac.uk.
  • Boot-Handford RP; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, UK. Electronic address: ray.boothandford@manchester.ac.uk.
  • Hardingham TE; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, UK. Electronic address: tim.hardingham@manchester.ac.uk.
Osteoarthritis Cartilage ; 24(8): 1431-40, 2016 08.
Article in En | MEDLINE | ID: mdl-26973327
OBJECTIVES: Joint degeneration in osteoarthritis (OA) is characterised by damage and loss of articular cartilage. The pattern of loss is consistent with damage occurring only where the mechanical loading is high. We have investigated using RNA-sequencing (RNA-seq) and systems analyses the changes that occur in damaged OA cartilage by comparing it with intact cartilage from the same joint. METHODS: Cartilage was obtained from eight OA patients undergoing total knee replacement. RNA was extracted from cartilage on the damaged distal medial condyle (DMC) and the intact posterior lateral condyle (PLC). RNA-seq was performed to identify differentially expressed genes (DEGs) and systems analyses applied to identify dysregulated pathways. RESULTS: In the damaged OA cartilage, there was decreased expression of chondrogenic genes SOX9, SOX6, COL11A2, COL9A1/2/3, ACAN and HAPLN1; increases in non-chondrogenic genes COL1A1, COMP and FN1; an altered pattern of secreted proteinase expression; but no expression of major inflammatory cytokines. Systems analyses by PhenomeExpress revealed significant sub-networks of DEGs including mitotic cell cycle, Wnt signalling, apoptosis and matrix organisation that were influenced by a core of altered transcription factors (TFs), FOSL1, AHR, E2F1 and FOXM1. CONCLUSIONS: Gene expression changes in damaged cartilage suggested a signature non-chondrogenic response of altered matrix protein and secreted proteinase expression. There was evidence of a damage response in this late OA cartilage, which surprisingly showed features detected experimentally in the early response of cartilage to mechanical overload. PhenomeExpress analysis identified a hub of DEGs linked by a core of four differentially regulated TFs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoarthritis, Knee Type of study: Prognostic_studies Limits: Humans Language: En Journal: Osteoarthritis Cartilage Journal subject: ORTOPEDIA / REUMATOLOGIA Year: 2016 Document type: Article Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoarthritis, Knee Type of study: Prognostic_studies Limits: Humans Language: En Journal: Osteoarthritis Cartilage Journal subject: ORTOPEDIA / REUMATOLOGIA Year: 2016 Document type: Article Country of publication: Reino Unido