Fibromodulin-null murine knee joints display increased incidences of osteoarthritis and alterations in tissue biochemistry

被引:39
作者
Gill, MR
Oldberg, Å
Reinholt, FP [1 ]
机构
[1] Univ Oslo, Rikshosp Univ Hosp, Inst Pathol, NO-0027 Oslo, Norway
[2] Univ Oslo, Rikshosp Univ Hosp, Dept Pathol, Oslo, Norway
[3] Lund Univ, Dept Cell & Mol Biol, Lund, Sweden
关键词
osteoarthritis; fibromodulin; lumican; knock-out mice; transmission electron microscopy; articular cartilage; ligaments;
D O I
10.1053/joca.2002.0527
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To elucidate variations in tissue ultrastructure and incidence of pathology between fibromodulin (FM)-null mice and wild-type (WT) animals. Design: FM-null and WT siblings from different age groups were compared. Serial sections were made through paraffin-embedded whole knees and investigated histologically. Additionally, medial femoral condyle peaks from sibling pairs were investigated ultrastructurally using transmission electron microscopy. Results: Histological findings demonstrated a clear and increasing disparity between tissue degeneration in WT and FM-null animal knees with progressing age. Distinct differences were apparent by 36 weeks. Around the 80 week period and onward these differences became profound. However, qualitative ultrastructural investigation did not indicate either any aberrant tissue ultrastructure or any abnormal collagen fibril forms in FM-null articular cartilage compared with WT. Biochemical and immunohistochemical investigation of FM-null articular cartilage showed a significant increase in tissue levels of lumican (LUM). Conversely, the cruciate ligaments of the knee showed both an increase in LUM content and considerable structural abnormalities including the tendency towards rupture. Conclusion: This report indicates for the first time that FM-null mice have a higher propensity towards degenerative changes in their knee joints than comparable WT animals. Interestingly, no underlying ultrastructural or fibril abnormalities within the articular cartilage could be identified to explain why FM-null cartilage is more prone to pathological changes than wild-type tissue. We conclude that alterations in ligaments, and possibly other tissues within the knee, are of considerable importance in the pathogenesis of the observed articular cartilage degeneration. (C) 2002 OsteoArthritis Research Society International. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:751 / 757
页数:7
相关论文
共 21 条
[1]   Collagen remodeling in the anterior cruciate ligament associated with developing spontaneous murine osteoarthritis [J].
Anderson-MacKenzie, JM ;
Billingham, ME ;
Bailey, AJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 258 (03) :763-767
[2]  
ANTONSSON P, 1991, J BIOL CHEM, V266, P16859
[3]  
BAYLISS MT, 1978, BIOCHEM J, V176, P638
[4]   Lumican regulates collagen fibril assembly: Skin fragility and corneal opacity in the absence of lumican [J].
Chakravarti, S ;
Magnuson, T ;
Lass, JH ;
Jepsen, KJ ;
LaMantia, C ;
Carroll, H .
JOURNAL OF CELL BIOLOGY, 1998, 141 (05) :1277-1286
[5]   Targeted disruption of decorin leads to abnormal collagen fibril morphology and skin fragility [J].
Danielson, KG ;
Baribault, H ;
Holmes, DF ;
Graham, H ;
Kadler, KE ;
Iozzo, RV .
JOURNAL OF CELL BIOLOGY, 1997, 136 (03) :729-743
[6]   Differential expression of lumican and fibromodulin regulate collagen fibrillogenesis in developing mouse tendons [J].
Ezura, Y ;
Chakravarti, S ;
Oldberg, Å ;
Chervoneva, I ;
Birk, DE .
JOURNAL OF CELL BIOLOGY, 2000, 151 (04) :779-787
[7]   Structural requirements for fibromodulin binding to collagen and the control of type I collagen fibrillogenesis - Critical roles for disulphide bonding and the C-terminal region [J].
Font, B ;
Eichenberger, D ;
Goldschmidt, D ;
Boutillon, MM ;
Hulmes, DJS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 254 (03) :580-587
[8]   THE HUMAN LUMICAN GENE - ORGANIZATION, CHROMOSOMAL, LOCATION, AND EXPRESSION IN ARTICULAR-CARTILAGE [J].
GROVER, J ;
CHEN, XN ;
KORENBERG, JR ;
ROUGHLEY, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21942-21949
[9]  
HEDBOM E, 1989, J BIOL CHEM, V264, P6898
[10]   Association of the aggrecan keratan sulfate-rich region with collagen in bovine articular cartilage [J].
Hedlund, H ;
Hedbom, E ;
Heinegard, D ;
Mengarelli-Widholm, S ;
Reinholt, FP ;
Svensson, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5777-5781