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Erschienen in: Rheumatology International 1/2008

01.11.2008 | Original Article

Expression of MMP-1 in cartilage and synovium of experimentally induced rabbit ACLT traumatic osteoarthritis: immunohistochemical study

verfasst von: Hongbin Wu, Jingyuan Du, Qixin Zheng

Erschienen in: Rheumatology International | Ausgabe 1/2008

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Abstract

To observe the level and the distribution of MMP-1 in cartilage and synovium over the progression of OA in rabbit ACLT model, and to explore the relationship between the amount of MMP-1 expression and the degree of OA cartilage degradation. OA was induced in 20 rabbits by anterior cruciate ligament transection (ACLT) and ten rabbits were killed at 4 and 8 weeks after the operation, respectively. A further ten rabbits received unilateral knee arthrotomy as controls. Cartilage degradation was observed under dissecting microscope, immunohistochemical, and morphometric analysis were adopted to record the tissue level and distribution of MMP-1 in cartilage and synovium. Cartilage degradation in both ACLT groups was more severe than that in control group, and the degradation in 8-week ACLT group was more severe than that in 4-week ACLT group. MMP-1 was expressed predominantly in the superficial and upper intermediate layers of cartilage and in the lining layer of synovium. Its expression was increased steadily over the progression of OA both in cartilage and in synovium, but there was a little difference in the increase pattern between them: increase of MMP-1 in synovium lagged behind that in cartilage in early stage of OA. Conclusion: MMP-1 was involved in OA development in rabbit ACLT model and the amount of its expression was related with the degree of cartilage degradation. The increase of MMP-1 expression in synovium lagged behind that in cartilage, suggesting OA pathology was originated from cartilage, but synovitis may also paticipate in cartilage degradation, especially in middle and late stage of OA.
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Literatur
2.
Zurück zum Zitat Rengel Y, Ospelt C, Gay S (2007) Proteinases in the joint: clinical relevance of proteinases in joint destruction. Arthritis Res Ther 9(5):221 Rengel Y, Ospelt C, Gay S (2007) Proteinases in the joint: clinical relevance of proteinases in joint destruction. Arthritis Res Ther 9(5):221
3.
Zurück zum Zitat Dean DD, Martel-Pelletier J, Pelletier JP, Howell DS, Woessner JF Jr (1989) Evidence for metalloproteinase and metalloproteinase inhibitor imbalance in human osteoarthritic cartilage. J Clin Invest 84:678–685. doi:10.1172/JCI114215 PubMedCrossRef Dean DD, Martel-Pelletier J, Pelletier JP, Howell DS, Woessner JF Jr (1989) Evidence for metalloproteinase and metalloproteinase inhibitor imbalance in human osteoarthritic cartilage. J Clin Invest 84:678–685. doi:10.​1172/​JCI114215 PubMedCrossRef
6.
Zurück zum Zitat Fernandes JC, Martel-Pelletier J, Lascau-Coman V et al (1998) Collagenase-1 and collagenase-3 synthesis in normal and early experimental osteoarthritic canine cartilage: an immunohistochemical study. J Rheumatol 25(8):1585–1594PubMed Fernandes JC, Martel-Pelletier J, Lascau-Coman V et al (1998) Collagenase-1 and collagenase-3 synthesis in normal and early experimental osteoarthritic canine cartilage: an immunohistochemical study. J Rheumatol 25(8):1585–1594PubMed
7.
Zurück zum Zitat Chung L, Shimokawa K, Dinakarpandian D et al (2000) Identification of the 183 RWTNNFREY191 region as a critical segment of matrix metalloproteinase 1 for the expression of collagenolytic activity. J Biol Chem 275:29610–29617. doi:10.1074/jbc.M004039200 PubMedCrossRef Chung L, Shimokawa K, Dinakarpandian D et al (2000) Identification of the 183 RWTNNFREY191 region as a critical segment of matrix metalloproteinase 1 for the expression of collagenolytic activity. J Biol Chem 275:29610–29617. doi:10.​1074/​jbc.​M004039200 PubMedCrossRef
8.
Zurück zum Zitat Fiorito S, Magrini L, Adrey J, Brouty-Boyé D et al (2005) Inflammatory status and cartilage regenerative potential of synovial fibroblasts from patients with osteoarthritis and chondropathy. Rheumatology (Oxford) 44(2):164–171. doi:10.1093/rheumatology/keh431 CrossRef Fiorito S, Magrini L, Adrey J, Brouty-Boyé D et al (2005) Inflammatory status and cartilage regenerative potential of synovial fibroblasts from patients with osteoarthritis and chondropathy. Rheumatology (Oxford) 44(2):164–171. doi:10.​1093/​rheumatology/​keh431 CrossRef
11.
Zurück zum Zitat Pelletier JP, Jovanovic D, Fernandes JC et al (1998) Reduced progression of experimental osteoarthritis in vivo by selective inhibition of inducible nitric oxide synthase. Arthritis Rheum 41(7):1275–1286. doi :10.1002/1529-0131(199807)41:7<1275::AID-ART19>3.0.CO;2-TPubMedCrossRef Pelletier JP, Jovanovic D, Fernandes JC et al (1998) Reduced progression of experimental osteoarthritis in vivo by selective inhibition of inducible nitric oxide synthase. Arthritis Rheum 41(7):1275–1286. doi :10.1002/1529-0131(199807)41:7<1275::AID-ART19>3.0.CO;2-TPubMedCrossRef
12.
Zurück zum Zitat Pelletier JP, Lascau-Coman V, Jovanovic D et al (1999) Selective inhibition of inducible nitric oxide synthase in experimental oateoarthritis is associated with reduction in tissue levels of catabolic factors. J Rheumatol 26(9):2002–2014PubMed Pelletier JP, Lascau-Coman V, Jovanovic D et al (1999) Selective inhibition of inducible nitric oxide synthase in experimental oateoarthritis is associated with reduction in tissue levels of catabolic factors. J Rheumatol 26(9):2002–2014PubMed
13.
Zurück zum Zitat Shlopov BV, Smith GN Jr, Cole AA et al (1999) Differential patterns of response to doxycycline and transforming growth factor beta1 in the down-regulation of collagenases in osteoarthritic and normal human chondrocytes. Arthritis Rheum 42(4):719–727. doi :10.1002/1529-0131(199904)42:4<719::AID-ANR15>3.0.CO;2-TPubMedCrossRef Shlopov BV, Smith GN Jr, Cole AA et al (1999) Differential patterns of response to doxycycline and transforming growth factor beta1 in the down-regulation of collagenases in osteoarthritic and normal human chondrocytes. Arthritis Rheum 42(4):719–727. doi :10.1002/1529-0131(199904)42:4<719::AID-ANR15>3.0.CO;2-TPubMedCrossRef
14.
Zurück zum Zitat Tetlow LC, Adlam DJ, Woolley DE (2001) Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage: associations with degenerative changes. Arthritis Rheum 44(3):585–594. doi :10.1002/1529-0131(200103)44:3<585::AID-ANR107>3.0.CO;2-CPubMedCrossRef Tetlow LC, Adlam DJ, Woolley DE (2001) Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage: associations with degenerative changes. Arthritis Rheum 44(3):585–594. doi :10.1002/1529-0131(200103)44:3<585::AID-ANR107>3.0.CO;2-CPubMedCrossRef
15.
Zurück zum Zitat Freemont AJ, Hampson V, Tilman R et al (1997) Gene expression of matrix metalloproteinases 1, 3, and 9 by chondrocytes in osteoarthritic human knee articular cartilage is zone and grade specific. Ann Rheum Dis 56(9):542–549PubMedCrossRef Freemont AJ, Hampson V, Tilman R et al (1997) Gene expression of matrix metalloproteinases 1, 3, and 9 by chondrocytes in osteoarthritic human knee articular cartilage is zone and grade specific. Ann Rheum Dis 56(9):542–549PubMedCrossRef
16.
Zurück zum Zitat Brandt KD, Braunstein EM, Visco DM et al (1991) Anterior (cranial) cruciate ligament transection in the dog: a bona fide model of osteoarthritis, not merely of cartilage injury and repair. J Rheumatol 18(3):436–446PubMed Brandt KD, Braunstein EM, Visco DM et al (1991) Anterior (cranial) cruciate ligament transection in the dog: a bona fide model of osteoarthritis, not merely of cartilage injury and repair. J Rheumatol 18(3):436–446PubMed
18.
Zurück zum Zitat Hollander AP, Pidoux I, Reiner A et al (1995) Damage to type II collagen in aging and osteoarthritis starts at the articular surface, originates round chondrocytes, and extends into the cartilage with progressive degeneration. J Clin Invest 96(6):2859–2869. doi:10.1172/JCI118357 PubMedCrossRef Hollander AP, Pidoux I, Reiner A et al (1995) Damage to type II collagen in aging and osteoarthritis starts at the articular surface, originates round chondrocytes, and extends into the cartilage with progressive degeneration. J Clin Invest 96(6):2859–2869. doi:10.​1172/​JCI118357 PubMedCrossRef
19.
Zurück zum Zitat Young L, Katrib A, Cuello C et al (2001) Effects of intraarticular glucocorticoids on macrophage infiltration and mediators of joint damage in osteoarthritis synovial membranes: findings in a double-blind, placebo-controlled study. Arthritis Rheum 44(2):343–350. doi :10.1002/1529-0131(200102)44:2<343::AID-ANR52>3.0.CO;2-QPubMedCrossRef Young L, Katrib A, Cuello C et al (2001) Effects of intraarticular glucocorticoids on macrophage infiltration and mediators of joint damage in osteoarthritis synovial membranes: findings in a double-blind, placebo-controlled study. Arthritis Rheum 44(2):343–350. doi :10.1002/1529-0131(200102)44:2<343::AID-ANR52>3.0.CO;2-QPubMedCrossRef
20.
Zurück zum Zitat Pelletier JP, Faure MP, Dibattisa JA et al (1993) Coordinate synthesis of stromylisine, interleukin-1 and oncogene proteins in experimental osteoarthritis. An immunohistochemical study. Am J Pathol 142(1):95–105PubMed Pelletier JP, Faure MP, Dibattisa JA et al (1993) Coordinate synthesis of stromylisine, interleukin-1 and oncogene proteins in experimental osteoarthritis. An immunohistochemical study. Am J Pathol 142(1):95–105PubMed
Metadaten
Titel
Expression of MMP-1 in cartilage and synovium of experimentally induced rabbit ACLT traumatic osteoarthritis: immunohistochemical study
verfasst von
Hongbin Wu
Jingyuan Du
Qixin Zheng
Publikationsdatum
01.11.2008
Verlag
Springer-Verlag
Erschienen in
Rheumatology International / Ausgabe 1/2008
Print ISSN: 0172-8172
Elektronische ISSN: 1437-160X
DOI
https://doi.org/10.1007/s00296-008-0636-2

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