Open AccessTime‐series transcriptional profiling yields new perspectives on susceptibility to murine osteoarthritis
Author(s) -
Poulet Blandine,
Ulici Veronica,
Stone Timothy C.,
Pead Matthew,
Gburcik Valentina,
Constantinou Eleni,
Palmer Donald B.,
Beier Frank,
Timmons James A.,
Pitsillides Andrew A.
Publication year - 2012
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.34572
Subject(s) - transcriptome , osteoarthritis , gene expression profiling , phenotype , biology , cartilage , gene expression , microarray , gene , medicine , immunology , bioinformatics , pathology , genetics , anatomy , alternative medicine
Objective Chronological age is a powerful epidemiologic risk factor for osteoarthritis (OA), a multifactorial disease that is characterized by articular cartilage (AC) degradation. It is unclear from a molecular perspective how aging interacts with OA to produce this risk to AC integrity. To address this key question, we used in vivo time‐course analysis of OA development and murine interstrain variability in natural susceptibility to OA to examine changes in non–OA‐prone CBA mice versus OA‐prone STR/Ort mice, which develop disease that bears significant histologic resemblance to human OA. Through global transcriptome profiling, we attempted to discover the molecular signature linked with both OA vulnerability and progression. Methods Affymetrix Mouse Gene 1.0 ST Array profiles were generated from AC samples derived from CBA and STR/Ort mice at 3 different ages, corresponding to the stages prior to, at, and late after the natural onset of OA in the STR/Ort mice. Results We found that the OA in STR/Ort mice exhibited a molecular phenotype resembling human OA, and we pinpointed a central role of NF‐κB signaling and the emergence of an immune‐related signature in OA cartilage over time. We discovered that, strikingly, young healthy AC has a highly expressed skeletal muscle gene expression program, which is switched off during maturation, but is intriguingly retained in AC during OA development in STR/Ort mice. Conclusion This study is the first to show that AC chondrocytes share a high‐abundance gene‐expression program with skeletal muscle. We show that failure to switch this program off, as well as the restoration of this program, is associated with inappropriate expression of NF‐κB signaling pathways, skeletal muscle–related genes, and induction and/or progression of OA.