» Articles » PMID: 19103633

Gene Expression in Human Chondrocytes in Late Osteoarthritis is Changed in Both Fibrillated and Intact Cartilage Without Evidence of Generalised Chondrocyte Hypertrophy

Overview
Journal Ann Rheum Dis
Specialty Rheumatology
Date 2008 Dec 24
PMID 19103633
Citations 64
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: To investigate changes in gene expression in fibrillated and intact human osteoarthritis (OA) cartilage for evidence of an altered chondrocyte phenotype and hypertrophy.

Methods: Paired osteochondral samples were taken from a high-load site and a low-load site from 25 OA joints and were compared with eight similar paired samples from age-matched controls. Gene expression of key matrix and regulatory genes was analysed by quantitative real-time reverse transcription-polymerase chain reaction on total RNA extracted from the cartilage.

Results: There was a major change in chondrocyte gene expression in OA cartilage. SOX9 (38-fold) and aggrecan (4-fold) gene expression were both lower in OA (p<0.001), and collagen I (17-fold) and II (2.5-fold) gene expression were each increased in a subset of OA samples. The major changes in gene expression were similar at the fibrillated high-loaded site and the intact low-loaded site. There was no evidence of a generalised change in OA to proliferative or hypertrophic phenotype as seen in the growth plate, as genes associated with either stage of differentiation were unchanged (PTHrPR), or significantly downregulated (collagen X (14-fold, p<0.002), VEGF (23-fold, p<0.02), BCL-2 (5.6-fold, p<0.001), matrilin-1 (6.5-fold, p<0.001)). In contrast MMP-13 was significantly upregulated in the OA cartilage samples (5.3-fold, p<0.003).

Conclusions: The expression of key chondrocyte genes, including aggrecan and SOX9, was decreased in OA cartilage and the changes were similar in both fibrillated high-loaded and intact low-loaded cartilage on the same joint. However, there was no significant upregulation of type X collagen, and other genes associated with chondrocyte further differentiation and hypertrophy.

Citing Articles

A versatile platform based on matrix metalloproteinase-sensitive peptides for novel diagnostic and therapeutic strategies in arthritis.

Li M, Deng T, Chen Q, Jiang S, Li H, Li J Bioact Mater. 2025; 47:100-120.

PMID: 39897588 PMC: 11787566. DOI: 10.1016/j.bioactmat.2025.01.011.


FTO-mediated SMAD2 m6A modification protects cartilage against Osteoarthritis.

Zhou H, Xie Z, Qian Y, Ni W, Cui L, Fang X Exp Mol Med. 2024; 56(10):2283-2295.

PMID: 39363112 PMC: 11542000. DOI: 10.1038/s12276-024-01330-y.


Articular cartilage corefucosylation regulates tissue resilience in osteoarthritis.

Homan K, Onodera T, Hanamatsu H, Furukawa J, Momma D, Matsuoka M Elife. 2024; 12.

PMID: 38466626 PMC: 10928514. DOI: 10.7554/eLife.92275.


Re-thinking osteoarthritis pathogenesis: what can we learn (and what do we need to unlearn) from mouse models about the mechanisms involved in disease development.

Poulsen R, Jain L, Dalbeth N Arthritis Res Ther. 2023; 25(1):59.

PMID: 37046337 PMC: 10100340. DOI: 10.1186/s13075-023-03042-6.


Evaluating the Effect of Hypoxia on Human Adult Mesenchymal Stromal Cell Chondrogenesis In Vitro A Systematic Review.

Ranmuthu C, Ranmuthu C, Wijewardena C, Seah M, Khan W Int J Mol Sci. 2022; 23(23).

PMID: 36499531 PMC: 9741425. DOI: 10.3390/ijms232315210.