Aggrecan degradation in osteoarthritis and rheumatoid arthritis
Lark, Michael W. ; Bayne, Ellen K. and Lohmander, L. Stefan LU
(1995)
In Acta Orthopaedica
66(S266).
p.92-97
- Abstract
Aggrecan turnover is critically important to maintain extracellular matrix homeostasis in articular cartilage. Cartilage aggrecan metabolism has been studied in chondrocyte cell cultures, cartilage explant cultures, and in whole animal models. In many of these studies, matrix metalloproteinases (MMPs) are proposed to degrade cartilage aggrecan. MMP expression appears elevated in joint tissues from patients with osteoarthritis (OA) and rheumatoid arthritis (RA) (Dean et al. 1989, Wolfe et al. 1993) and inhibitors of both MMPs and thiol proteinases have been shown to block aggrecan (Buttle et al. 1992) and type II collagen (Mort et al. 1993) degradation in cartilage explant cultures. Using antibodies and cDNA probes, elevations in... (More)
Aggrecan turnover is critically important to maintain extracellular matrix homeostasis in articular cartilage. Cartilage aggrecan metabolism has been studied in chondrocyte cell cultures, cartilage explant cultures, and in whole animal models. In many of these studies, matrix metalloproteinases (MMPs) are proposed to degrade cartilage aggrecan. MMP expression appears elevated in joint tissues from patients with osteoarthritis (OA) and rheumatoid arthritis (RA) (Dean et al. 1989, Wolfe et al. 1993) and inhibitors of both MMPs and thiol proteinases have been shown to block aggrecan (Buttle et al. 1992) and type II collagen (Mort et al. 1993) degradation in cartilage explant cultures. Using antibodies and cDNA probes, elevations in expression and concentration of many of these enzymes in animal models and in OA and RA have been described. Human cartilage aggrecan has now been cloned and sequenced (Doege et al. 1991). This information, in combination with the ability to sequence aggrecan and aggrecan fragments at the protein level, has resulted in the identification of several aggrecan fragments which appear to result from proteinase degradation. In this report, we describe data which suggest that MMPs may in part be responsible for aggrecan catabolism in normal articular cartilage, as well as in the elevated catabolism seen in OA and RA.
(Less)
- author
- Lark, Michael W.
; Bayne, Ellen K.
and Lohmander, L. Stefan
LU
- organization
- publishing date
- 1995
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Acta Orthopaedica
- volume
- 66
- issue
- S266
- pages
- 6 pages
- publisher
- Taylor & Francis
- external identifiers
-
- pmid:8553869
- scopus:0029385397
- ISSN
- 1745-3674
- DOI
- 10.3109/17453679509157660
- language
- English
- LU publication?
- yes
- id
- 42f61329-e53f-46dd-b6f4-83ec15791c65
- date added to LUP
- 2016-05-04 23:47:51
- date last changed
- 2024-01-04 02:52:47
@article{42f61329-e53f-46dd-b6f4-83ec15791c65,
abstract = {{<p>Aggrecan turnover is critically important to maintain extracellular matrix homeostasis in articular cartilage. Cartilage aggrecan metabolism has been studied in chondrocyte cell cultures, cartilage explant cultures, and in whole animal models. In many of these studies, matrix metalloproteinases (MMPs) are proposed to degrade cartilage aggrecan. MMP expression appears elevated in joint tissues from patients with osteoarthritis (OA) and rheumatoid arthritis (RA) (Dean et al. 1989, Wolfe et al. 1993) and inhibitors of both MMPs and thiol proteinases have been shown to block aggrecan (Buttle et al. 1992) and type II collagen (Mort et al. 1993) degradation in cartilage explant cultures. Using antibodies and cDNA probes, elevations in expression and concentration of many of these enzymes in animal models and in OA and RA have been described. Human cartilage aggrecan has now been cloned and sequenced (Doege et al. 1991). This information, in combination with the ability to sequence aggrecan and aggrecan fragments at the protein level, has resulted in the identification of several aggrecan fragments which appear to result from proteinase degradation. In this report, we describe data which suggest that MMPs may in part be responsible for aggrecan catabolism in normal articular cartilage, as well as in the elevated catabolism seen in OA and RA.</p>}},
author = {{Lark, Michael W. and Bayne, Ellen K. and Lohmander, L. Stefan}},
issn = {{1745-3674}},
language = {{eng}},
number = {{S266}},
pages = {{92--97}},
publisher = {{Taylor & Francis}},
series = {{Acta Orthopaedica}},
title = {{Aggrecan degradation in osteoarthritis and rheumatoid arthritis}},
url = {{http://dx.doi.org/10.3109/17453679509157660}},
doi = {{10.3109/17453679509157660}},
volume = {{66}},
year = {{1995}},
}