Metabolic activity and gene expression of osteoarthritic chondrocytes in correlation with radiological and histological characteristics

被引:7
作者
Stoeve, Johannes
Gremmes, Christina
Guenther, Klaus Peter
Scharf, Hanns-Peter
Schwarz, Markus
机构
[1] Heidelberg Univ, Fac Clin Med, Dept Orthopaed Surg, D-68167 Mannheim, Germany
[2] Horse Clin Juhnde, Juhnde, Germany
[3] Univ Dresden, Dept Orthopaed Surg, Dresden, Germany
关键词
cartilage; osteoarthritis; proteoglycan; metalloproteinase; gene expression;
D O I
10.1016/j.biopha.2006.09.005
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of this study was to analyze metabolic activity of osteoarthritic chondrocytes in correlation with radiographic, histologic and gene expression data. Six patients with osteoarthritis (OA) of the knee were analyzed clinically and radiographically (Kellgren and Lawrence, K&L). During total knee replacement surgery cartilage samples from the medial and lateral condyles and tibial plateaus were separately harvested. Specimen were analyzed histologically (Mankin Score) and total RNA was extracted. Steady state levels of stromelysin (MMP-3), aggrecan (AGG) and the house-keeping gene beta-actin were measured using quantitative PCR. In order to estimate metabolic activity chondrocytes were cultured in alginate beads and proteoglycan content was measured after I week. PG content in cultures was dependent from degradation status of cartilage (medial compartments 20.4 +/- 0.83 ng/ng, lateral compartments 29.9 +/- 3.0 ng/ng P < 0.01). We found a positive correlation of PG content in cultures with Mankin's grading (r=0.79; P < 0.01) and with K&L scoring (r=0.57; P=0.05). There was a considerable variation of expression levels of MMP-3 and AGG. PG metabolism of cultured chondrocytes correlated only with the macroscopic and microscopic degradation status of cartilage. Gene expression showed a high variability and no correlation to PG metabolism indicating a more complex regulation. (c) 2006 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:644 / 647
页数:4
相关论文
共 22 条
[1]   Molecular pathology and pathobiology of osteoarthritic cartilage [J].
Aigner, T ;
McKenna, L .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (01) :5-18
[2]  
Aigner T, 2001, ARTHRITIS RHEUM-US, V44, P2777, DOI 10.1002/1529-0131(200112)44:12<2777::AID-ART465>3.0.CO
[3]  
2-H
[4]   Phenotypic modulation of chondrocytes as a potential therapeutic target in osteoarthritis: A hypothesis [J].
Aigner, T ;
Dudhia, J .
ANNALS OF THE RHEUMATIC DISEASES, 1997, 56 (05) :287-291
[5]   Suppression of cartilage matrix gene expression in upper zone chondrocytes of osteoarthritic cartilage [J].
Aigner, T ;
Vornehm, SI ;
Zeiler, G ;
Dudhia, J ;
vonderMark, K ;
Bayliss, MT .
ARTHRITIS AND RHEUMATISM, 1997, 40 (03) :562-569
[6]   MICRODETERMINATION OF PROTEOGLYCANS AND GLYCOSAMINOGLYCANS IN THE PRESENCE OF GUANIDINE-HYDROCHLORIDE [J].
CHANDRASEKHAR, S ;
ESTERMAN, MA ;
HOFFMAN, HA .
ANALYTICAL BIOCHEMISTRY, 1987, 161 (01) :103-108
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]  
Di Cesare PE, 1999, J ORTHOPAED RES, V17, P437
[9]  
Dieppe P, 1995, ACTA ORTHOP SCAND, V66, P1
[10]   Gene expression of matrix metalloproteinases 1, 3, and 9 by chondrocytes in osteoarthritic human knee articular cartilage is zone and grade specific [J].
Freemont, AJ ;
Hampson, V ;
Tilman, R ;
Goupille, P ;
Taiwo, Y ;
Hoyland, JA .
ANNALS OF THE RHEUMATIC DISEASES, 1997, 56 (09) :542-549