» Articles » PMID: 11787822

A Degeneration-based Hypothesis for Interpreting Fibrillar Changes in the Osteoarthritic Cartilage Matrix

Overview
Journal J Anat
Date 2002 Jan 15
PMID 11787822
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The collagen fibrillar architectures in the general matrix of cartilage slices removed from both normal and osteoarthritic femoral heads were examined by both differential interference light microscopy and scanning electron microscopy. Whereas the normal general matrix contained a finely differentiated pseudo-random weave of fibrils developed from an interconnected array of radial elements, the osteoarthritic general matrix was characterised by the presence of structurally distinct regions consisting of strongly aligned radial bundles of fibrils and associated intense tangles or 'knotted' features. Simple structural models were developed to explore possible transformation structures based on two different types of interconnectivity in the three-dimensional fibrillar network. These models support the hypothesis that the distinctive ultrastructural features of the osteoarthritic general matrix can develop as a consequence of largely passive degradative changes occurring in the fibrillar weave originally present in the normal matrix. This could, in principle, occur independently of any new structure that might develop as a consequence of any upregulation of collagen associated with the osteoarthritic process.

Citing Articles

The ultrastructure of cartilage tissue and its swelling response in relation to matrix health.

Brown E, Simons J, Thambyah A J Anat. 2021; 240(1):107-119.

PMID: 34333796 PMC: 8655166. DOI: 10.1111/joa.13527.


Protein Levels and Microstructural Changes in Localized Regions of Early Cartilage Degeneration Compared with Adjacent Intact Cartilage.

Jacob B, Jullig M, Middleditch M, Payne L, Broom N, Sarojini V Cartilage. 2018; 12(2):192-210.

PMID: 30486653 PMC: 7970373. DOI: 10.1177/1947603518809401.


Comparison between in vitro and in vivo cartilage overloading studies based on a systematic literature review.

Nickien M, Heuijerjans A, Ito K, van Donkelaar C J Orthop Res. 2018; .

PMID: 29644716 PMC: 6120482. DOI: 10.1002/jor.23910.


The Impact of Collagen Fibril Polarity on Second Harmonic Generation Microscopy.

Couture C, Bancelin S, van der Kolk J, Popov K, Rivard M, Legare K Biophys J. 2015; 109(12):2501-2510.

PMID: 26682809 PMC: 4699883. DOI: 10.1016/j.bpj.2015.10.040.


How a radial focal incision influences the internal shear distribution in articular cartilage with respect to its zonally differentiated microanatomy.

Nickien M, Thambyah A, Broom N J Anat. 2015; 227(3):315-24.

PMID: 26198817 PMC: 4560566. DOI: 10.1111/joa.12350.


References
1.
Lane J, Weiss C . Review of articular cartilage collagen research. Arthritis Rheum. 1975; 18(6):553-62. DOI: 10.1002/art.1780180605. View

2.
Maroudas A . Balance between swelling pressure and collagen tension in normal and degenerate cartilage. Nature. 1976; 260(5554):808-9. DOI: 10.1038/260808a0. View

3.
Vignon E, Arlot M, Meunier P, Vignon G . Quantitative histological changes in osteoarthritic hip cartilage. Morphometric analysis of 29 osteoarthritic and 26 normal human femoral heads. Clin Orthop Relat Res. 1974; (103):269-78. View

4.
Pond M, Nuki G . Experimentally-induced osteoarthritis in the dog. Ann Rheum Dis. 1973; 32(4):387-8. PMC: 1006123. DOI: 10.1136/ard.32.4.387. View

5.
Ruttner J, Spycher M . Electron microscopic investigations on aging and osteoarthrotic human cartilage. Preliminary report. Pathol Microbiol (Basel). 1968; 31(1):14-24. DOI: 10.1159/000162000. View