Skip to main content
Erschienen in: Arthritis Research & Therapy 2/2003

01.03.2003 | Review

Aggrecanases and cartilage matrix degradation

verfasst von: Hideaki Nagase, Masahide Kashiwagi

Erschienen in: Arthritis Research & Therapy | Ausgabe 2/2003

Einloggen, um Zugang zu erhalten

Abstract

The loss of extracellular matrix macromolecules from the cartilage results in serious impairment of joint function. Metalloproteinases called 'aggrecanases' that cleave the Glu373–Ala374 bond of the aggrecan core protein play a key role in the early stages of cartilage destruction in rheumatoid arthritis and in osteoarthritis. Three members of the ADAMTS family of proteinases, ADAMTS-1, ADAMTS-4 and ADAMTS-5, have been identified as aggrecanases. Matrix metalloproteinases, which are also found in arthritic joints, cleave aggrecans, but at a distinct site from the aggrecanases (i.e. Asn341–Phe342). The present review discuss the enzymatic properties of the three known aggrecanases, the regulation of their activities, and their role in cartilage matrix breakdown during the development of arthritis in relation to the action of matrix metalloproteinases.
Literatur
1.
Zurück zum Zitat Hinegård D, Lorenzo P, Sanxe T: Matrix glycoprotein, proteoglycans, and cartilage. In Kelly's Textbook of Rheumatology. Edited by: Ruddy S, Harris ED Jr, Sledge CB. 2001, Philadelphia: WB Saunders Company, 41-53. Hinegård D, Lorenzo P, Sanxe T: Matrix glycoprotein, proteoglycans, and cartilage. In Kelly's Textbook of Rheumatology. Edited by: Ruddy S, Harris ED Jr, Sledge CB. 2001, Philadelphia: WB Saunders Company, 41-53.
2.
Zurück zum Zitat Evans CH, Brown TD: Role of physical and medical aspects in degradating the matrix. In Joint Cartilage Degradation: Basic and Clinical Aspects. Edited by: Woessner JF Jr, Howell DS. 1993, New York: Marcel Dekker, 187-208. Evans CH, Brown TD: Role of physical and medical aspects in degradating the matrix. In Joint Cartilage Degradation: Basic and Clinical Aspects. Edited by: Woessner JF Jr, Howell DS. 1993, New York: Marcel Dekker, 187-208.
3.
Zurück zum Zitat Burkhardt H, Schwingel M, Menninger H, Macartney HW, Tschesche H: Oxygen radicals as effectors of cartilage destruction. Direct degradative effect on matrix components and indirect action via activation of latent collagenase from polymorphonuclear leukocytes. Arthritis Rheum. 1986, 29: 379-387.PubMed Burkhardt H, Schwingel M, Menninger H, Macartney HW, Tschesche H: Oxygen radicals as effectors of cartilage destruction. Direct degradative effect on matrix components and indirect action via activation of latent collagenase from polymorphonuclear leukocytes. Arthritis Rheum. 1986, 29: 379-387.PubMed
4.
Zurück zum Zitat Okada Y: Proteinase and matrix degradation. In Kelly's Textbook of Rheumatology. Edited by: Ruddy S, Harris ED Jr, Sledge CB. 2001, Philadelphia: WB Saunders Company, 55-72. Okada Y: Proteinase and matrix degradation. In Kelly's Textbook of Rheumatology. Edited by: Ruddy S, Harris ED Jr, Sledge CB. 2001, Philadelphia: WB Saunders Company, 55-72.
5.
Zurück zum Zitat Tetlow LC, Adlam DJ, Woolley DE: Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage: associations with degenerative changes. Arthritis Rheum. 2001, 44: 585-594. 10.1002/1529-0131(200103)44:3<585::AID-ANR107>3.3.CO;2-3.PubMed Tetlow LC, Adlam DJ, Woolley DE: Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage: associations with degenerative changes. Arthritis Rheum. 2001, 44: 585-594. 10.1002/1529-0131(200103)44:3<585::AID-ANR107>3.3.CO;2-3.PubMed
6.
Zurück zum Zitat Dean DD, Martel-Pelletier J, Pelletier JP, Howell DS, Woessner JF: Evidence for metalloproteinase and metalloproteinase inhibitor imbalance in human osteoarthritic cartilage. J Clin Invest. 1989, 84: 678-685.PubMedCentralPubMed Dean DD, Martel-Pelletier J, Pelletier JP, Howell DS, Woessner JF: Evidence for metalloproteinase and metalloproteinase inhibitor imbalance in human osteoarthritic cartilage. J Clin Invest. 1989, 84: 678-685.PubMedCentralPubMed
7.
Zurück zum Zitat Caterson B, Flannery CR, Hughes CE, Little CB: Mechanisms involved in cartilage proteoglycan catabolism. Matrix Biol. 2000, 19: 333-344. 10.1016/S0945-053X(00)00078-0.PubMed Caterson B, Flannery CR, Hughes CE, Little CB: Mechanisms involved in cartilage proteoglycan catabolism. Matrix Biol. 2000, 19: 333-344. 10.1016/S0945-053X(00)00078-0.PubMed
8.
Zurück zum Zitat Mort JS, Billington CJ: Articular cartilage and changes in arthritis: matrix degradation. Arthritis Res. 2001, 3: 337-341. 10.1186/ar325.PubMedCentralPubMed Mort JS, Billington CJ: Articular cartilage and changes in arthritis: matrix degradation. Arthritis Res. 2001, 3: 337-341. 10.1186/ar325.PubMedCentralPubMed
9.
Zurück zum Zitat Nagase H: Aggrecanase in cartilage matrix breakdown. Connective Tissue. 2001, 33: 27-32. Nagase H: Aggrecanase in cartilage matrix breakdown. Connective Tissue. 2001, 33: 27-32.
10.
Zurück zum Zitat Arner EC: Aggrecanase-mediated cartilage degradation. Curr Opin Pharmacol. 2002, 2: 322-329. 10.1016/S1471-4892(02)00148-0.PubMed Arner EC: Aggrecanase-mediated cartilage degradation. Curr Opin Pharmacol. 2002, 2: 322-329. 10.1016/S1471-4892(02)00148-0.PubMed
11.
Zurück zum Zitat Roughley PJ, Mort JS: Catabolism of proteoglycans. In Proteoglygans. Structure, Biology, and Molecular Interactions. Edited by: Iozzo RV. 2000, New York: Marcel Dekker, 93-113. Roughley PJ, Mort JS: Catabolism of proteoglycans. In Proteoglygans. Structure, Biology, and Molecular Interactions. Edited by: Iozzo RV. 2000, New York: Marcel Dekker, 93-113.
12.
Zurück zum Zitat Fosang AJ, Neame PJ, Hardingham TE, Murphy G, Hamilton JA: Cleavage of cartilage proteoglycan between G1 and G2 domains by stromelysins. J Biol Chem. 1991, 266: 15579-15582.PubMed Fosang AJ, Neame PJ, Hardingham TE, Murphy G, Hamilton JA: Cleavage of cartilage proteoglycan between G1 and G2 domains by stromelysins. J Biol Chem. 1991, 266: 15579-15582.PubMed
13.
Zurück zum Zitat Fosang AJ, Neame PJ, Last K, Hardingham TE, Murphy G, Hamilton JA: The interglobular domain of cartilage aggrecan is cleaved by PUMP, gelatinases, and cathepsin B. J Biol Chem. 1992, 267: 19470-19474.PubMed Fosang AJ, Neame PJ, Last K, Hardingham TE, Murphy G, Hamilton JA: The interglobular domain of cartilage aggrecan is cleaved by PUMP, gelatinases, and cathepsin B. J Biol Chem. 1992, 267: 19470-19474.PubMed
14.
Zurück zum Zitat Flannery CR, Lark MW, Sandy JD: Identification of a stromelysin cleavage site within the interglobular domain of human aggrecan. Evidence for proteolysis at this site in vivo in human articular cartilage. J Biol Chem. 1992, 267: 1008-1014.PubMed Flannery CR, Lark MW, Sandy JD: Identification of a stromelysin cleavage site within the interglobular domain of human aggrecan. Evidence for proteolysis at this site in vivo in human articular cartilage. J Biol Chem. 1992, 267: 1008-1014.PubMed
15.
Zurück zum Zitat Sandy JD, Neame PJ, Boynton RE, Flannery CR: Catabolism of aggrecan in cartilage explants. Identification of a major cleavage site within the interglobular domain. J Biol Chem. 1991, 266: 8683-8685.PubMed Sandy JD, Neame PJ, Boynton RE, Flannery CR: Catabolism of aggrecan in cartilage explants. Identification of a major cleavage site within the interglobular domain. J Biol Chem. 1991, 266: 8683-8685.PubMed
16.
Zurück zum Zitat Ilic MZ, Handley CJ, Robinson HC, Mok MT: Mechanism of catabolism of aggrecan by articular cartilage. Arch Biochem Biophys. 1992, 294: 115-122. 10.1016/0003-9861(92)90144-L.PubMed Ilic MZ, Handley CJ, Robinson HC, Mok MT: Mechanism of catabolism of aggrecan by articular cartilage. Arch Biochem Biophys. 1992, 294: 115-122. 10.1016/0003-9861(92)90144-L.PubMed
17.
Zurück zum Zitat Loulakis P, Shrikhande A, Davis G, Maniglia CA: N-terminal sequence of proteoglycan fragments isolated from medium of interleukin-1-treated articular-cartilage cultures. Putative site(s) of enzymic cleavage. Biochem J. 1992, 284: 589-593.PubMedCentralPubMed Loulakis P, Shrikhande A, Davis G, Maniglia CA: N-terminal sequence of proteoglycan fragments isolated from medium of interleukin-1-treated articular-cartilage cultures. Putative site(s) of enzymic cleavage. Biochem J. 1992, 284: 589-593.PubMedCentralPubMed
18.
Zurück zum Zitat Sandy JD, Flannery CR, Neame PJ, Lohmander LS: The structure of aggrecan fragments in human synovial fluid. Evidence for the involvement in osteoarthritis of a novel proteinase which cleaves the Glu 373–Ala 374 bond of the interglobular domain. J Clin Invest. 1992, 89: 1512-1516.PubMedCentralPubMed Sandy JD, Flannery CR, Neame PJ, Lohmander LS: The structure of aggrecan fragments in human synovial fluid. Evidence for the involvement in osteoarthritis of a novel proteinase which cleaves the Glu 373–Ala 374 bond of the interglobular domain. J Clin Invest. 1992, 89: 1512-1516.PubMedCentralPubMed
19.
Zurück zum Zitat Lohmander LS, Neame PJ, Sandy JD: The structure of aggrecan fragments in human synovial fluid. Evidence that aggrecanase mediates cartilage degradation in inflammatory joint disease, joint injury, and osteoarthritis. Arthritis Rheum. 1993, 36: 1214-1222.PubMed Lohmander LS, Neame PJ, Sandy JD: The structure of aggrecan fragments in human synovial fluid. Evidence that aggrecanase mediates cartilage degradation in inflammatory joint disease, joint injury, and osteoarthritis. Arthritis Rheum. 1993, 36: 1214-1222.PubMed
20.
Zurück zum Zitat Tortorella MD, Burn TC, Pratta MA, Abbaszade I, Hollis JM, Liu R, Rosenfeld SA, Copeland RA, Decicco CP, Wynn R, Rockwell A, Yang F, Duke JL, Solomon K, George H, Bruckner R, Nagase H, Itoh Y, Ellis DM, Ross H, Wiswall BH, Murphy K, Hillman MC, Hollis GF, Arner EC: Purification and cloning of aggrecanase-1: a member of the ADAMTS family of proteins. Science. 1999, 284: 1664-1666. 10.1126/science.284.5420.1664.PubMed Tortorella MD, Burn TC, Pratta MA, Abbaszade I, Hollis JM, Liu R, Rosenfeld SA, Copeland RA, Decicco CP, Wynn R, Rockwell A, Yang F, Duke JL, Solomon K, George H, Bruckner R, Nagase H, Itoh Y, Ellis DM, Ross H, Wiswall BH, Murphy K, Hillman MC, Hollis GF, Arner EC: Purification and cloning of aggrecanase-1: a member of the ADAMTS family of proteins. Science. 1999, 284: 1664-1666. 10.1126/science.284.5420.1664.PubMed
21.
Zurück zum Zitat Abbaszade I, Liu RQ, Yang F, Rosenfeld SA, Ross OH, Link JR, Ellis DM, Tortorella MD, Pratta MA, Hollis JM, Wynn R, Duke JL, George HJ, Hillman MC, Murphy K, Wiswall BH, Copeland RA, Decicco CP, Bruckner R, Nagase H, Itoh Y, Newton RC, Magolda RL, Trzaskos JM, Burn TC: Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family. J Biol Chem. 1999, 274: 23443-23450. 10.1074/jbc.274.33.23443.PubMed Abbaszade I, Liu RQ, Yang F, Rosenfeld SA, Ross OH, Link JR, Ellis DM, Tortorella MD, Pratta MA, Hollis JM, Wynn R, Duke JL, George HJ, Hillman MC, Murphy K, Wiswall BH, Copeland RA, Decicco CP, Bruckner R, Nagase H, Itoh Y, Newton RC, Magolda RL, Trzaskos JM, Burn TC: Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family. J Biol Chem. 1999, 274: 23443-23450. 10.1074/jbc.274.33.23443.PubMed
22.
Zurück zum Zitat Tang BL: ADAMTS: a novel family of extracellular matrix proteases. Int J Biochem Cell Biol. 2001, 33: 33-44. 10.1016/S1357-2725(00)00061-3.PubMed Tang BL: ADAMTS: a novel family of extracellular matrix proteases. Int J Biochem Cell Biol. 2001, 33: 33-44. 10.1016/S1357-2725(00)00061-3.PubMed
23.
Zurück zum Zitat Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, Lóez-Otín C: Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains. Gene. 2002, 283: 49-62. 10.1016/S0378-1119(01)00861-7.PubMed Cal S, Obaya AJ, Llamazares M, Garabaya C, Quesada V, Lóez-Otín C: Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains. Gene. 2002, 283: 49-62. 10.1016/S0378-1119(01)00861-7.PubMed
24.
Zurück zum Zitat Kuno K, Okada Y, Kawashima H, Nakamura H, Miyasaka M, Ohno H, Matsushima K: ADAMTS-1 cleaves a cartilage proteoglycan, aggrecan. FEBS Lett. 2000, 478: 241-245. 10.1016/S0014-5793(00)01854-8.PubMed Kuno K, Okada Y, Kawashima H, Nakamura H, Miyasaka M, Ohno H, Matsushima K: ADAMTS-1 cleaves a cartilage proteoglycan, aggrecan. FEBS Lett. 2000, 478: 241-245. 10.1016/S0014-5793(00)01854-8.PubMed
25.
Zurück zum Zitat Rodríguez-Manzaneque JC, Westling J, Thai SN, Luque A, Knäuper V, Murphy G, Sandy JD, Iruela-Arispe ML: ADAMTS1 cleaves aggrecan at multiple sites and is differentially inhibited by metalloproteinase inhibitors. Biochem Biophys Res Commun. 2002, 293: 501-508. 10.1016/S0006-291X(02)00254-1.PubMed Rodríguez-Manzaneque JC, Westling J, Thai SN, Luque A, Knäuper V, Murphy G, Sandy JD, Iruela-Arispe ML: ADAMTS1 cleaves aggrecan at multiple sites and is differentially inhibited by metalloproteinase inhibitors. Biochem Biophys Res Commun. 2002, 293: 501-508. 10.1016/S0006-291X(02)00254-1.PubMed
26.
Zurück zum Zitat Flannery CR, Little CB, Hughes CE, Caterson B: Expression of ADAMTS homologues in articular cartilage. Biochem Biophys Res Commun. 1999, 260: 318-322. 10.1006/bbrc.1999.0909.PubMed Flannery CR, Little CB, Hughes CE, Caterson B: Expression of ADAMTS homologues in articular cartilage. Biochem Biophys Res Commun. 1999, 260: 318-322. 10.1006/bbrc.1999.0909.PubMed
27.
Zurück zum Zitat Rawling ND, O'Brien EA, Barrett AJ: MEROPS: the protease database. Nucleic Acids Res. 2002, 70: 343-346. 10.1093/nar/30.1.343. Rawling ND, O'Brien EA, Barrett AJ: MEROPS: the protease database. Nucleic Acids Res. 2002, 70: 343-346. 10.1093/nar/30.1.343.
30.
Zurück zum Zitat Blobel CP, Wolfsberg TG, Turck CW, Myles DG, Primakoff P, White JM: A potential fusion peptide and an integrin ligand domain in a protein active in sperm-egg fusion. Nature. 1992, 356: 248-252. 10.1038/356248a0.PubMed Blobel CP, Wolfsberg TG, Turck CW, Myles DG, Primakoff P, White JM: A potential fusion peptide and an integrin ligand domain in a protein active in sperm-egg fusion. Nature. 1992, 356: 248-252. 10.1038/356248a0.PubMed
31.
Zurück zum Zitat Yagami-Hiromasa T, Sato T, Kurisaki T, Kamijo K, Nabeshima Y, Fujisawa-Sehara A: A metalloprotease-disintegrin participating in myoblast fusion. Nature. 1995, 377: 652-656. 10.1038/377652a0.PubMed Yagami-Hiromasa T, Sato T, Kurisaki T, Kamijo K, Nabeshima Y, Fujisawa-Sehara A: A metalloprotease-disintegrin participating in myoblast fusion. Nature. 1995, 377: 652-656. 10.1038/377652a0.PubMed
32.
Zurück zum Zitat Asakura M, Kitakaze M, Takashima S, Liao Y, Ishikura F, Yoshinaka T, Ohmoto H, Node K, Yoshino K, Ishiguro H, Asanuma H, Sanada S, Matsumura Y, Takeda H, Beppu S, Tada M, Hori M, Higashiyama S: Cardiac hypertrophy is inhibited by antagonism of ADAM12 processing of HB-EGF: metalloproteinase inhibitors as a new therapy. Nat Med. 2002, 8: 35-40. 10.1038/nm0102-35.PubMed Asakura M, Kitakaze M, Takashima S, Liao Y, Ishikura F, Yoshinaka T, Ohmoto H, Node K, Yoshino K, Ishiguro H, Asanuma H, Sanada S, Matsumura Y, Takeda H, Beppu S, Tada M, Hori M, Higashiyama S: Cardiac hypertrophy is inhibited by antagonism of ADAM12 processing of HB-EGF: metalloproteinase inhibitors as a new therapy. Nat Med. 2002, 8: 35-40. 10.1038/nm0102-35.PubMed
33.
Zurück zum Zitat Pan D, Rubin GM: Kuzbanian controls proteolytic processing of Notch and mediates lateral inhibition during Drosophila and vertebrate neurogenesis. Cell. 1997, 90: 271-280. 10.1016/S0092-8674(00)80335-9.PubMed Pan D, Rubin GM: Kuzbanian controls proteolytic processing of Notch and mediates lateral inhibition during Drosophila and vertebrate neurogenesis. Cell. 1997, 90: 271-280. 10.1016/S0092-8674(00)80335-9.PubMed
34.
Zurück zum Zitat Qi H, Rand MD, Wu X, Sestan N, Wang W, Rakic P, Xu T, Artavanis-Tsakonas S: Processing of the notch ligand delta by the metalloprotease Kuzbanian. Science. 1999, 283: 91-94. 10.1126/science.283.5398.91.PubMed Qi H, Rand MD, Wu X, Sestan N, Wang W, Rakic P, Xu T, Artavanis-Tsakonas S: Processing of the notch ligand delta by the metalloprotease Kuzbanian. Science. 1999, 283: 91-94. 10.1126/science.283.5398.91.PubMed
35.
Zurück zum Zitat Black RA, Rauch CT, Kozlosky CJ, Peschon JJ, Slack JL, Wolfson MF, Castner BJ, Stocking KL, Reddy P, Srinivasan S, Nelson N, Boiani N, Schooley KA, Gerhart M, Davis R, Fitzner JN, Johnson RS, Paxton RJ, March CJ, Cerretti DP: A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells. Nature. 1997, 385: 729-733. 10.1038/385729a0.PubMed Black RA, Rauch CT, Kozlosky CJ, Peschon JJ, Slack JL, Wolfson MF, Castner BJ, Stocking KL, Reddy P, Srinivasan S, Nelson N, Boiani N, Schooley KA, Gerhart M, Davis R, Fitzner JN, Johnson RS, Paxton RJ, March CJ, Cerretti DP: A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells. Nature. 1997, 385: 729-733. 10.1038/385729a0.PubMed
36.
Zurück zum Zitat Moss ML, Jin SL, Milla ME, Bickett DM, Burkhart W, Carter HL, Chen WJ, Clay WC, Didsbury JR, Hassler D, Hoffman CR, Kost TA, Lambert MH, Leesnitzer MA, McCauley P, McGeehan G, Mitchell J, Moyer M, Pahel G, Rocque W, Overton LK, Schoenen F, Seaton T, Su JL, Warner J, Willard D, Becherer JD: Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha. Nature. 1997, 385: 733-736. 10.1038/385733a0.PubMed Moss ML, Jin SL, Milla ME, Bickett DM, Burkhart W, Carter HL, Chen WJ, Clay WC, Didsbury JR, Hassler D, Hoffman CR, Kost TA, Lambert MH, Leesnitzer MA, McCauley P, McGeehan G, Mitchell J, Moyer M, Pahel G, Rocque W, Overton LK, Schoenen F, Seaton T, Su JL, Warner J, Willard D, Becherer JD: Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha. Nature. 1997, 385: 733-736. 10.1038/385733a0.PubMed
37.
Zurück zum Zitat Nardi JB, Martos R, Walden KK, Lampe DJ, Robertson HM: Expression of lacunin, a large multidomain extracellular matrix protein, accompanies morphogenesis of epithelial monolayers in Manduca sexta. Insect Biochem Mol Biol. 1999, 29: 883-897. 10.1016/S0965-1748(99)00064-8.PubMed Nardi JB, Martos R, Walden KK, Lampe DJ, Robertson HM: Expression of lacunin, a large multidomain extracellular matrix protein, accompanies morphogenesis of epithelial monolayers in Manduca sexta. Insect Biochem Mol Biol. 1999, 29: 883-897. 10.1016/S0965-1748(99)00064-8.PubMed
38.
Zurück zum Zitat Bork P, Beckmann G: The CUB domain. A widespread module in developmentally regulated proteins. J Mol Biol. 1993, 231: 539-545. 10.1006/jmbi.1993.1305.PubMed Bork P, Beckmann G: The CUB domain. A widespread module in developmentally regulated proteins. J Mol Biol. 1993, 231: 539-545. 10.1006/jmbi.1993.1305.PubMed
39.
Zurück zum Zitat Colige A, Beschin A, Samyn B, Goebels Y, van Beeumen J, Nusgens BV, Lapière CM: Characterization and partial amino acid sequencing of a 107-kDa procollagen I N-proteinase purified by affinity chromatography on immobilized type XIV collagen. J Biol Chem. 1995, 270: 16724-16730. 10.1074/jbc.270.28.16724.PubMed Colige A, Beschin A, Samyn B, Goebels Y, van Beeumen J, Nusgens BV, Lapière CM: Characterization and partial amino acid sequencing of a 107-kDa procollagen I N-proteinase purified by affinity chromatography on immobilized type XIV collagen. J Biol Chem. 1995, 270: 16724-16730. 10.1074/jbc.270.28.16724.PubMed
40.
Zurück zum Zitat Fernandes RJ, Hirohata S, Engle JM, Colige A, Cohn DH, Eyre DR, Apte SS: Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis. J Biol Chem. 2001, 276: 31502-31509. 10.1074/jbc.M103466200.PubMed Fernandes RJ, Hirohata S, Engle JM, Colige A, Cohn DH, Eyre DR, Apte SS: Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis. J Biol Chem. 2001, 276: 31502-31509. 10.1074/jbc.M103466200.PubMed
41.
Zurück zum Zitat Colige A, Vandenberghe I, Thiry M, Lambert CA, van Beeumen J, Li SW, Prockop DJ, Lapière CM, Nusgens BV: Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3. J Biol Chem. 2002, 277: 5756-5766. 10.1074/jbc.M105601200.PubMed Colige A, Vandenberghe I, Thiry M, Lambert CA, van Beeumen J, Li SW, Prockop DJ, Lapière CM, Nusgens BV: Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3. J Biol Chem. 2002, 277: 5756-5766. 10.1074/jbc.M105601200.PubMed
42.
Zurück zum Zitat Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD, Ginsburg D, Tsai HM: Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001, 413: 488-494. 10.1038/35097008.PubMed Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD, Ginsburg D, Tsai HM: Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001, 413: 488-494. 10.1038/35097008.PubMed
43.
Zurück zum Zitat Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, Krause M, Scharrer I, Aumann V, Mittler U, Solenthaler M, Lammle B: von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med. 1998, 339: 1578-1584. 10.1056/NEJM199811263392202.PubMed Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, Krause M, Scharrer I, Aumann V, Mittler U, Solenthaler M, Lammle B: von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med. 1998, 339: 1578-1584. 10.1056/NEJM199811263392202.PubMed
44.
Zurück zum Zitat Tsai HM, Lian EC: Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med. 1998, 339: 1585-1594. 10.1056/NEJM199811263392203.PubMedCentralPubMed Tsai HM, Lian EC: Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med. 1998, 339: 1585-1594. 10.1056/NEJM199811263392203.PubMedCentralPubMed
45.
Zurück zum Zitat Vazquez F, Hastings G, Ortega MA, Lane TF, Oikemus S, Lombardo M, Iruela-Arispe ML: METH-1, a human ortholog of ADAMTS-1, and METH-2 are members of a new family of proteins with angio-inhibitory activity. J Biol Chem. 1999, 274: 23349-23357. 10.1074/jbc.274.33.23349.PubMed Vazquez F, Hastings G, Ortega MA, Lane TF, Oikemus S, Lombardo M, Iruela-Arispe ML: METH-1, a human ortholog of ADAMTS-1, and METH-2 are members of a new family of proteins with angio-inhibitory activity. J Biol Chem. 1999, 274: 23349-23357. 10.1074/jbc.274.33.23349.PubMed
46.
Zurück zum Zitat Tortorella MD, Pratta M, Liu RQ, Austin J, Ross OH, Abbaszade I, Burn T, Arner E: Sites of aggrecan cleavage by recombinant human aggrecanase-1 (ADAMTS-4). J Biol Chem. 2000, 275: 18566-18573. 10.1074/jbc.M909383199.PubMed Tortorella MD, Pratta M, Liu RQ, Austin J, Ross OH, Abbaszade I, Burn T, Arner E: Sites of aggrecan cleavage by recombinant human aggrecanase-1 (ADAMTS-4). J Biol Chem. 2000, 275: 18566-18573. 10.1074/jbc.M909383199.PubMed
47.
Zurück zum Zitat Tortorella MD, Liu RQ, Burn T, Newton RC, Arner E: Characterization of human aggrecanase 2 (ADAM-TS5): substrate specificity studies and comparison with aggrecanase 1 (ADAM-TS4). Matrix Biol. 2002, 21: 499-511. 10.1016/S0945-053X(02)00069-0.PubMed Tortorella MD, Liu RQ, Burn T, Newton RC, Arner E: Characterization of human aggrecanase 2 (ADAM-TS5): substrate specificity studies and comparison with aggrecanase 1 (ADAM-TS4). Matrix Biol. 2002, 21: 499-511. 10.1016/S0945-053X(02)00069-0.PubMed
48.
Zurück zum Zitat Vankemmelbeke MN, Holen I, Wilson AG, Ilic MZ, Handley CJ, Kelner GS, Clark M, Liu C, Maki RA, Burnett D, Buttle DJ: Expression and activity of ADAMTS-5 in synovium. Eur J Biochem. 2001, 268: 1259-1268. 10.1046/j.1432-1327.2001.01990.x.PubMed Vankemmelbeke MN, Holen I, Wilson AG, Ilic MZ, Handley CJ, Kelner GS, Clark M, Liu C, Maki RA, Burnett D, Buttle DJ: Expression and activity of ADAMTS-5 in synovium. Eur J Biochem. 2001, 268: 1259-1268. 10.1046/j.1432-1327.2001.01990.x.PubMed
49.
Zurück zum Zitat Westling J, Fosang AJ, Last K, Thompson VP, Tomkinson KN, Hebert T, McDonagh T, Collins-Racie LA, LaVallie ER, Morris EA, Sandy JD: ADAMTS4 cleaves at the aggrecanase site (Glu373–Ala374) and secondarily at the matrix metalloproteinase site (Asn341–Phe342) in the aggrecan interglobular domain. J Biol Chem. 2002, 277: 16059-16066. 10.1074/jbc.M108607200.PubMed Westling J, Fosang AJ, Last K, Thompson VP, Tomkinson KN, Hebert T, McDonagh T, Collins-Racie LA, LaVallie ER, Morris EA, Sandy JD: ADAMTS4 cleaves at the aggrecanase site (Glu373–Ala374) and secondarily at the matrix metalloproteinase site (Asn341–Phe342) in the aggrecan interglobular domain. J Biol Chem. 2002, 277: 16059-16066. 10.1074/jbc.M108607200.PubMed
50.
Zurück zum Zitat Sandy JD, Westling J, Kenagy RD, Iruela-Arispe ML, Verscharen C, Rodriguez-Mazaneque JC, Zimmermann DR, Lemire JM, Fischer JW, Wight TN, Clowes AW: Versican V1 proteolysis in human aorta in vivo occurs at the Glu441–Ala442 bond, a site that is cleaved by recombinant ADAMTS-1 and ADAMTS-4. J Biol Chem. 2001, 276: 13372-13378. 10.1074/jbc.M009737200.PubMed Sandy JD, Westling J, Kenagy RD, Iruela-Arispe ML, Verscharen C, Rodriguez-Mazaneque JC, Zimmermann DR, Lemire JM, Fischer JW, Wight TN, Clowes AW: Versican V1 proteolysis in human aorta in vivo occurs at the Glu441–Ala442 bond, a site that is cleaved by recombinant ADAMTS-1 and ADAMTS-4. J Biol Chem. 2001, 276: 13372-13378. 10.1074/jbc.M009737200.PubMed
51.
Zurück zum Zitat Kuno K, Terashima Y, Matsushima K: ADAMTS-1 is an active metalloproteinase associated with the extracellular matrix. J Biol Chem. 1999, 274: 18821-18826. 10.1074/jbc.274.26.18821.PubMed Kuno K, Terashima Y, Matsushima K: ADAMTS-1 is an active metalloproteinase associated with the extracellular matrix. J Biol Chem. 1999, 274: 18821-18826. 10.1074/jbc.274.26.18821.PubMed
52.
Zurück zum Zitat Matthews RT, Gary SC, Zerillo C, Pratta M, Solomon K, Arner EC, Hockfield S: Brain-enriched hyaluronan binding (BEHAB)/brevican cleavage in a glioma cell line is mediated by a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) family member. J Biol Chem. 2000, 275: 22695-22703. 10.1074/jbc.M909764199.PubMed Matthews RT, Gary SC, Zerillo C, Pratta M, Solomon K, Arner EC, Hockfield S: Brain-enriched hyaluronan binding (BEHAB)/brevican cleavage in a glioma cell line is mediated by a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) family member. J Biol Chem. 2000, 275: 22695-22703. 10.1074/jbc.M909764199.PubMed
53.
Zurück zum Zitat Barret AJ: α2-Macroglobulin. Methods Enzymol. 1981, 80: 737-754. Barret AJ: α2-Macroglobulin. Methods Enzymol. 1981, 80: 737-754.
54.
Zurück zum Zitat Tortorella M, Pratta M, Liu RQ, Abbaszade I, Ross H, Burn T, Arner E: The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage. J Biol Chem. 2000, 275: 25791-25797. 10.1074/jbc.M001065200.PubMed Tortorella M, Pratta M, Liu RQ, Abbaszade I, Ross H, Burn T, Arner E: The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage. J Biol Chem. 2000, 275: 25791-25797. 10.1074/jbc.M001065200.PubMed
55.
Zurück zum Zitat Pratta MA, Tortorella MD, Arner EC: Age-related changes in aggrecan glycosylation affect cleavage by aggrecanase. J Biol Chem. 2000, 275: 39096-39102. 10.1074/jbc.M006201200.PubMed Pratta MA, Tortorella MD, Arner EC: Age-related changes in aggrecan glycosylation affect cleavage by aggrecanase. J Biol Chem. 2000, 275: 39096-39102. 10.1074/jbc.M006201200.PubMed
56.
Zurück zum Zitat Hörber C, Buttner FH, Kern C, Schmiedeknecht G, Bartnik E: Truncation of the amino-terminus of the recombinant aggrecan rAgg1mut leads to reduced cleavage at the aggrecanase site. Efficient aggrecanase catabolism may depend on multiple substrate interactions. Matrix Biol. 2000, 19: 533-543. 10.1016/S0945-053X(00)00113-X.PubMed Hörber C, Buttner FH, Kern C, Schmiedeknecht G, Bartnik E: Truncation of the amino-terminus of the recombinant aggrecan rAgg1mut leads to reduced cleavage at the aggrecanase site. Efficient aggrecanase catabolism may depend on multiple substrate interactions. Matrix Biol. 2000, 19: 533-543. 10.1016/S0945-053X(00)00113-X.PubMed
57.
Zurück zum Zitat Mercuri FA, Maciewicz RA, Tart J, Last K, Fosang AJ: Mutations in the interglobular domain of aggrecan alter matrix metalloproteinase and aggrecanase cleavage patterns. Evidence that matrix metalloproteinase cleavage interferes with aggrecanase activity. J Biol Chem. 2000, 275: 33038-33045. 10.1074/jbc.275.42.33038.PubMed Mercuri FA, Maciewicz RA, Tart J, Last K, Fosang AJ: Mutations in the interglobular domain of aggrecan alter matrix metalloproteinase and aggrecanase cleavage patterns. Evidence that matrix metalloproteinase cleavage interferes with aggrecanase activity. J Biol Chem. 2000, 275: 33038-33045. 10.1074/jbc.275.42.33038.PubMed
58.
Zurück zum Zitat Rodríguez-Manzaneque JC, Milchanowski AB, Dufour EK, Leduc R, Iruela-Arispe ML: Characterization of METH-1/ADAMTS1 processing reveals two distinct active forms. J Biol Chem. 2000, 275: 33471-33479. 10.1074/jbc.M002599200.PubMed Rodríguez-Manzaneque JC, Milchanowski AB, Dufour EK, Leduc R, Iruela-Arispe ML: Characterization of METH-1/ADAMTS1 processing reveals two distinct active forms. J Biol Chem. 2000, 275: 33471-33479. 10.1074/jbc.M002599200.PubMed
59.
Zurück zum Zitat Gao G, Westling J, Thompson VP, Howell TD, Gottschall PE, Sandy JD: Activation of the proteolytic activity of ADAMTS4 (aggrecanase-1) by C-terminal truncation. J Biol Chem. 2002, 277: 11034-11041. 10.1074/jbc.M107443200.PubMed Gao G, Westling J, Thompson VP, Howell TD, Gottschall PE, Sandy JD: Activation of the proteolytic activity of ADAMTS4 (aggrecanase-1) by C-terminal truncation. J Biol Chem. 2002, 277: 11034-11041. 10.1074/jbc.M107443200.PubMed
60.
Zurück zum Zitat Arner EC, Pratta MA, Trzaskos JM, Decicco CP, Tortorella MD: Generation and characterization of aggrecanase. A soluble, cartilage-derived aggrecan-degrading activity. J Biol Chem. 1999, 274: 6594-6601. 10.1074/jbc.274.10.6594.PubMed Arner EC, Pratta MA, Trzaskos JM, Decicco CP, Tortorella MD: Generation and characterization of aggrecanase. A soluble, cartilage-derived aggrecan-degrading activity. J Biol Chem. 1999, 274: 6594-6601. 10.1074/jbc.274.10.6594.PubMed
61.
Zurück zum Zitat Kashiwagi M, Tortorella M, Nagase H, Brew K: TIMP-3 is a potent inhibitor of aggrecanase 1 (ADAM-TS4) and aggrecanase 2 (ADAM-TS5). J Biol Chem. 2001, 276: 12501-12504. 10.1074/jbc.C000848200.PubMed Kashiwagi M, Tortorella M, Nagase H, Brew K: TIMP-3 is a potent inhibitor of aggrecanase 1 (ADAM-TS4) and aggrecanase 2 (ADAM-TS5). J Biol Chem. 2001, 276: 12501-12504. 10.1074/jbc.C000848200.PubMed
62.
Zurück zum Zitat Hashimoto G, Aoki T, Nakamura H, Tanzawa K, Okada Y: Inhibition of ADAMTS4 (aggrecanase-1) by tissue inhibitors of metalloproteinases (TIMP-1, 2, 3 and 4). FEBS Lett. 2001, 494: 192-195. 10.1016/S0014-5793(01)02323-7.PubMed Hashimoto G, Aoki T, Nakamura H, Tanzawa K, Okada Y: Inhibition of ADAMTS4 (aggrecanase-1) by tissue inhibitors of metalloproteinases (TIMP-1, 2, 3 and 4). FEBS Lett. 2001, 494: 192-195. 10.1016/S0014-5793(01)02323-7.PubMed
63.
Zurück zum Zitat Amour A, Slocombe PM, Webster A, Butler M, Knight CG, Smith BJ, Stephens PE, Shelley C, Hutton M, Knäuper V, Docherty AJ, Murphy G: TNF-alpha converting enzyme (TACE) is inhibited by TIMP-3. FEBS Lett. 1998, 435: 39-44. 10.1016/S0014-5793(98)01031-X.PubMed Amour A, Slocombe PM, Webster A, Butler M, Knight CG, Smith BJ, Stephens PE, Shelley C, Hutton M, Knäuper V, Docherty AJ, Murphy G: TNF-alpha converting enzyme (TACE) is inhibited by TIMP-3. FEBS Lett. 1998, 435: 39-44. 10.1016/S0014-5793(98)01031-X.PubMed
64.
Zurück zum Zitat Amour A, Knight CG, Webster A, Slocombe PM, Stephens PE, Knäuper V, Docherty AJ, Murphy G: The in vitro activity of ADAM-10 is inhibited by TIMP-1 and TIMP-3. FEBS Lett. 2000, 473: 275-279. 10.1016/S0014-5793(00)01528-3.PubMed Amour A, Knight CG, Webster A, Slocombe PM, Stephens PE, Knäuper V, Docherty AJ, Murphy G: The in vitro activity of ADAM-10 is inhibited by TIMP-1 and TIMP-3. FEBS Lett. 2000, 473: 275-279. 10.1016/S0014-5793(00)01528-3.PubMed
65.
Zurück zum Zitat Loechel F, Fox JW, Murphy G, Albrechtsen R, Wewer UM: ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3. Biochem Biophys Res Commun. 2000, 278: 511-515. 10.1006/bbrc.2000.3835.PubMed Loechel F, Fox JW, Murphy G, Albrechtsen R, Wewer UM: ADAM 12-S cleaves IGFBP-3 and IGFBP-5 and is inhibited by TIMP-3. Biochem Biophys Res Commun. 2000, 278: 511-515. 10.1006/bbrc.2000.3835.PubMed
66.
Zurück zum Zitat Yu WH, Yu S, Meng Q, Brew K, Woessner JF: TIMP-3 binds to sulfated glycosaminoglycans of the extracellular matrix. J Biol Chem. 2000, 275: 31226-31232. 10.1074/jbc.M000907200.PubMed Yu WH, Yu S, Meng Q, Brew K, Woessner JF: TIMP-3 binds to sulfated glycosaminoglycans of the extracellular matrix. J Biol Chem. 2000, 275: 31226-31232. 10.1074/jbc.M000907200.PubMed
67.
Zurück zum Zitat Apte SS, Hayashi K, Seldin MF, Mattei MG, Hayashi M, Olsen BR: Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10. Dev Dyn. 1994, 200: 177-197.PubMed Apte SS, Hayashi K, Seldin MF, Mattei MG, Hayashi M, Olsen BR: Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10. Dev Dyn. 1994, 200: 177-197.PubMed
68.
Zurück zum Zitat Su S, Grover J, Roughley PJ, DiBattista JA, Martel-Pelletier J, Pelletier JP, Zafarullah M: Expression of the tissue inhibitor of metalloproteinases (TIMP) gene family in normal and osteoarthritic joints. Rheumatol Int. 1999, 18: 183-191. 10.1007/s002960050083.PubMed Su S, Grover J, Roughley PJ, DiBattista JA, Martel-Pelletier J, Pelletier JP, Zafarullah M: Expression of the tissue inhibitor of metalloproteinases (TIMP) gene family in normal and osteoarthritic joints. Rheumatol Int. 1999, 18: 183-191. 10.1007/s002960050083.PubMed
69.
Zurück zum Zitat Su S, DiBattista JA, Sun Y, Li WQ, Zafarullah M: Up-regulation of tissue inhibitor of metalloproteinases-3 gene expression by TGF-beta in articular chondrocytes is mediated by serine/threonine and tyrosine kinases. J Cell Biochem. 1998, 70: 517-527. 10.1002/(SICI)1097-4644(19980915)70:4<517::AID-JCB8>3.3.CO;2-R.PubMed Su S, DiBattista JA, Sun Y, Li WQ, Zafarullah M: Up-regulation of tissue inhibitor of metalloproteinases-3 gene expression by TGF-beta in articular chondrocytes is mediated by serine/threonine and tyrosine kinases. J Cell Biochem. 1998, 70: 517-527. 10.1002/(SICI)1097-4644(19980915)70:4<517::AID-JCB8>3.3.CO;2-R.PubMed
70.
Zurück zum Zitat Li WQ, Zafarullah M: Oncostatin M up-regulates tissue inhibitor of metalloproteinases-3 gene expression in articular chondrocytes via de novo transcription, protein synthesis, and tyrosine kinase- and mitogen-activated protein kinase-dependent mechanisms. J Immunol. 1998, 161: 5000-5007.PubMed Li WQ, Zafarullah M: Oncostatin M up-regulates tissue inhibitor of metalloproteinases-3 gene expression in articular chondrocytes via de novo transcription, protein synthesis, and tyrosine kinase- and mitogen-activated protein kinase-dependent mechanisms. J Immunol. 1998, 161: 5000-5007.PubMed
71.
Zurück zum Zitat Takizawa M, Ohuchi E, Yamanaka H, Nakamura H, Ikeda E, Ghosh P, Okada Y: Production of tissue inhibitor of metalloproteinases 3 is selectively enhanced by calcium pentosan polysulfate in human rheumatoid synovial fibroblasts. Arthritis Rheum. 2000, 43: 812-820. 10.1002/1529-0131(200004)43:4<812::AID-ANR11>3.0.CO;2-Y.PubMed Takizawa M, Ohuchi E, Yamanaka H, Nakamura H, Ikeda E, Ghosh P, Okada Y: Production of tissue inhibitor of metalloproteinases 3 is selectively enhanced by calcium pentosan polysulfate in human rheumatoid synovial fibroblasts. Arthritis Rheum. 2000, 43: 812-820. 10.1002/1529-0131(200004)43:4<812::AID-ANR11>3.0.CO;2-Y.PubMed
72.
Zurück zum Zitat Munteanu SE, Ilic MZ, Handley CJ: Calcium pentosan polysulfate inhibits the catabolism of aggrecan in articular cartilage explant cultures. Arthritis Rheum. 2000, 43: 2211-2218. 10.1002/1529-0131(200010)43:10<2211::AID-ANR8>3.0.CO;2-D.PubMed Munteanu SE, Ilic MZ, Handley CJ: Calcium pentosan polysulfate inhibits the catabolism of aggrecan in articular cartilage explant cultures. Arthritis Rheum. 2000, 43: 2211-2218. 10.1002/1529-0131(200010)43:10<2211::AID-ANR8>3.0.CO;2-D.PubMed
73.
Zurück zum Zitat Munteanu SE, Ilic MZ, Handley CJ: Highly sulfated glycosaminoglycans inhibit aggrecanase degradation of aggrecan by bovine articular cartilage explant cultures. Matrix Biol. 2002, 21: 429-440. 10.1016/S0945-053X(02)00034-3.PubMed Munteanu SE, Ilic MZ, Handley CJ: Highly sulfated glycosaminoglycans inhibit aggrecanase degradation of aggrecan by bovine articular cartilage explant cultures. Matrix Biol. 2002, 21: 429-440. 10.1016/S0945-053X(02)00034-3.PubMed
74.
Zurück zum Zitat Arner EC, Pratta MA, Decicco CP, Xue CB, Newton RC, Trzaskos JM, Magolda RL, Tortorella MD: Aggrecanase. A target for the design of inhibitors of cartilage degradation. Ann NY Acad Sci. 1999, 878: 92-107.PubMed Arner EC, Pratta MA, Decicco CP, Xue CB, Newton RC, Trzaskos JM, Magolda RL, Tortorella MD: Aggrecanase. A target for the design of inhibitors of cartilage degradation. Ann NY Acad Sci. 1999, 878: 92-107.PubMed
75.
Zurück zum Zitat Yao W, Wasserman ZR, Chao M, Reddy G, Shi E, Liu RQ, Covington MB, Arner EC, Pratta MA, Tortorella M, Magolda RL, Newton R, Qian M, Ribadeneira MD, Christ D, Wexler RR, Decicco CP: Design and synthesis of a series of (2R)-N(4)-hydroxy-2-(3-hydroxybenzyl)-N(1)-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide derivatives as potent, selective, and orally bioavailable aggrecanase inhibitors. J Med Chem. 2001, 44: 3347-3350. 10.1021/jm015533c.PubMed Yao W, Wasserman ZR, Chao M, Reddy G, Shi E, Liu RQ, Covington MB, Arner EC, Pratta MA, Tortorella M, Magolda RL, Newton R, Qian M, Ribadeneira MD, Christ D, Wexler RR, Decicco CP: Design and synthesis of a series of (2R)-N(4)-hydroxy-2-(3-hydroxybenzyl)-N(1)-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide derivatives as potent, selective, and orally bioavailable aggrecanase inhibitors. J Med Chem. 2001, 44: 3347-3350. 10.1021/jm015533c.PubMed
76.
Zurück zum Zitat Yao W, Chao M, Wasserman ZR, Liu RQ, Covington MB, Newton R, Christ D, Wexler RR, Decicco CP: Potent P1' biphenylmethyl substituted aggrecanase inhibitors. Bioorg Med Chem Lett. 2002, 12: 101-104. 10.1016/S0960-894X(01)00704-1.PubMed Yao W, Chao M, Wasserman ZR, Liu RQ, Covington MB, Newton R, Christ D, Wexler RR, Decicco CP: Potent P1' biphenylmethyl substituted aggrecanase inhibitors. Bioorg Med Chem Lett. 2002, 12: 101-104. 10.1016/S0960-894X(01)00704-1.PubMed
77.
Zurück zum Zitat Cai L, Yin JP, Starovasnik MA, Hogue DA, Hillan KJ, Mort JS, Filvaroff EH: Pathways by which interleukin 17 induces articular cartilage breakdown in vitro and in vivo. Cytokine. 2001, 16: 10-21. 10.1006/cyto.2001.0939.PubMed Cai L, Yin JP, Starovasnik MA, Hogue DA, Hillan KJ, Mort JS, Filvaroff EH: Pathways by which interleukin 17 induces articular cartilage breakdown in vitro and in vivo. Cytokine. 2001, 16: 10-21. 10.1006/cyto.2001.0939.PubMed
78.
Zurück zum Zitat Sabatini M, Thomas M, Deschamps C, Lesur C, Rolland G, de Nanteuil G, Bonnet J: Effects of ceramide on aggrecanase activity in rabbit articular cartilage. Biochem Biophys Res Commun. 2001, 283: 1105-1110. 10.1006/bbrc.2001.4920.PubMed Sabatini M, Thomas M, Deschamps C, Lesur C, Rolland G, de Nanteuil G, Bonnet J: Effects of ceramide on aggrecanase activity in rabbit articular cartilage. Biochem Biophys Res Commun. 2001, 283: 1105-1110. 10.1006/bbrc.2001.4920.PubMed
79.
Zurück zum Zitat Stanton H, Ung L, Fosang AJ: The 45 kDa collagen-binding fragment of fibronectin induces matrix metalloproteinase-13 synthesis by chondrocytes and aggrecan degradation by aggrecanases. Biochem J. 2002, 364: 181-190.PubMedCentralPubMed Stanton H, Ung L, Fosang AJ: The 45 kDa collagen-binding fragment of fibronectin induces matrix metalloproteinase-13 synthesis by chondrocytes and aggrecan degradation by aggrecanases. Biochem J. 2002, 364: 181-190.PubMedCentralPubMed
80.
Zurück zum Zitat Bau B, Gebhard PM, Haag J, Knorr T, Bartnik E, Aigner T: Relative messenger RNA expression profiling of collagenases and aggrecanases in human articular chondrocytes in vivo and in vitro. Arthritis Rheum. 2002, 46: 2648-2657. 10.1002/art.10531.PubMed Bau B, Gebhard PM, Haag J, Knorr T, Bartnik E, Aigner T: Relative messenger RNA expression profiling of collagenases and aggrecanases in human articular chondrocytes in vivo and in vitro. Arthritis Rheum. 2002, 46: 2648-2657. 10.1002/art.10531.PubMed
81.
Zurück zum Zitat Curtis CL, Hughes CE, Flannery CR, Little CB, Harwood JL, Caterson B: n-3 fatty acids specifically modulate catabolic factors involved in articular cartilage degradation. J Biol Chem. 2000, 275: 721-724. 10.1074/jbc.275.2.721.PubMed Curtis CL, Hughes CE, Flannery CR, Little CB, Harwood JL, Caterson B: n-3 fatty acids specifically modulate catabolic factors involved in articular cartilage degradation. J Biol Chem. 2000, 275: 721-724. 10.1074/jbc.275.2.721.PubMed
82.
Zurück zum Zitat Tortorella MD, Malfait AM, Deccico C, Arner E: The role of ADAM-TS4 (aggrecanase-1) and ADAM-TS5 (aggrecanase-2) in a model of cartilage degradation. Osteoarthritis Cartilage. 2001, 9: 539-552. 10.1053/joca.2001.0427.PubMed Tortorella MD, Malfait AM, Deccico C, Arner E: The role of ADAM-TS4 (aggrecanase-1) and ADAM-TS5 (aggrecanase-2) in a model of cartilage degradation. Osteoarthritis Cartilage. 2001, 9: 539-552. 10.1053/joca.2001.0427.PubMed
83.
Zurück zum Zitat Little CB, Hughes CE, Curtis CL, Jones SA, Caterson B, Flannery CR: Cyclosporin A inhibition of aggrecanase-mediated proteoglycan catabolism in articular cartilage. Arthritis Rheum. 2002, 46: 124-129. 10.1002/1529-0131(200201)46:1<124::AID-ART10121>3.0.CO;2-X.PubMed Little CB, Hughes CE, Curtis CL, Jones SA, Caterson B, Flannery CR: Cyclosporin A inhibition of aggrecanase-mediated proteoglycan catabolism in articular cartilage. Arthritis Rheum. 2002, 46: 124-129. 10.1002/1529-0131(200201)46:1<124::AID-ART10121>3.0.CO;2-X.PubMed
84.
Zurück zum Zitat Koshy PJ, Lundy CJ, Rowan AD, Porter S, Edwards DR, Hogan A, Clark IM, Cawston TE: The modulation of matrix metalloproteinase and ADAM gene expression in human chondrocytes by interleukin-1 and oncostatin M: a time-course study using real-time quantitative reverse transcription-polymerase chain reaction. Arthritis Rheum. 2002, 46: 961-967. 10.1002/art.10212.PubMed Koshy PJ, Lundy CJ, Rowan AD, Porter S, Edwards DR, Hogan A, Clark IM, Cawston TE: The modulation of matrix metalloproteinase and ADAM gene expression in human chondrocytes by interleukin-1 and oncostatin M: a time-course study using real-time quantitative reverse transcription-polymerase chain reaction. Arthritis Rheum. 2002, 46: 961-967. 10.1002/art.10212.PubMed
85.
Zurück zum Zitat Yamanishi Y, Boyle DL, Clark M, Maki RA, Tortorella MD, Arner EC, Firestein GS: Expression and regulation of aggrecanase in arthritis: the role of TGF-beta. J Immunol. 2002, 168: 1405-1412.PubMed Yamanishi Y, Boyle DL, Clark M, Maki RA, Tortorella MD, Arner EC, Firestein GS: Expression and regulation of aggrecanase in arthritis: the role of TGF-beta. J Immunol. 2002, 168: 1405-1412.PubMed
86.
Zurück zum Zitat Curtis CL, Rees SG, Little CB, Flannery CR, Hughes CE, Wilson C, Dent CM, Otterness IG, Harwood JL, Caterson B: Pathologic indicators of degradation and inflammation in human osteoarthritic cartilage are abrogated by exposure to n-3 fatty acids. Arthritis Rheum. 2002, 46: 1544-1553. 10.1002/art.10305.PubMed Curtis CL, Rees SG, Little CB, Flannery CR, Hughes CE, Wilson C, Dent CM, Otterness IG, Harwood JL, Caterson B: Pathologic indicators of degradation and inflammation in human osteoarthritic cartilage are abrogated by exposure to n-3 fatty acids. Arthritis Rheum. 2002, 46: 1544-1553. 10.1002/art.10305.PubMed
87.
Zurück zum Zitat Lark MW, Bayne EK, Flanagan J, Harper CF, Hoerrner LA, Hutchinson NI, Singer II, Donatelli SA, Weidner JR, Williams HR, Mumford RA, Lohmander LS: Aggrecan degradation in human cartilage. Evidence for both matrix metalloproteinase and aggrecanase activity in normal, osteoarthritic, and rheumatoid joints. J Clin Invest. 1997, 100: 93-106.PubMedCentralPubMed Lark MW, Bayne EK, Flanagan J, Harper CF, Hoerrner LA, Hutchinson NI, Singer II, Donatelli SA, Weidner JR, Williams HR, Mumford RA, Lohmander LS: Aggrecan degradation in human cartilage. Evidence for both matrix metalloproteinase and aggrecanase activity in normal, osteoarthritic, and rheumatoid joints. J Clin Invest. 1997, 100: 93-106.PubMedCentralPubMed
88.
Zurück zum Zitat Fosang AJ, Last K, Maciewicz RA: Aggrecan is degraded by matrix metalloproteinases in human arthritis. Evidence that matrix metalloproteinase and aggrecanase activities can be independent. J Clin Invest. 1996, 98: 2292-2299.PubMedCentralPubMed Fosang AJ, Last K, Maciewicz RA: Aggrecan is degraded by matrix metalloproteinases in human arthritis. Evidence that matrix metalloproteinase and aggrecanase activities can be independent. J Clin Invest. 1996, 98: 2292-2299.PubMedCentralPubMed
89.
Zurück zum Zitat Little CB, Flannery CR, Hughes CE, Mort JS, Roughley PJ, Dent C, Caterson B: Aggrecanase versus matrix metalloproteinases in the catabolism of the interglobular domain of aggrecan in vitro. Biochem J. 1999, 344: 61-68. 10.1042/0264-6021:3440061.PubMedCentralPubMed Little CB, Flannery CR, Hughes CE, Mort JS, Roughley PJ, Dent C, Caterson B: Aggrecanase versus matrix metalloproteinases in the catabolism of the interglobular domain of aggrecan in vitro. Biochem J. 1999, 344: 61-68. 10.1042/0264-6021:3440061.PubMedCentralPubMed
90.
Zurück zum Zitat Little CB, Hughes CE, Curtis CL, Janusz MJ, Bohne R, Wang-Weigand S, Taiwo YO, Mitchell PG, Otterness IG, Flannery CR, Caterson B: Matrix metalloproteinases are involved in C-terminal and interglobular domain processing of cartilage aggrecan in late stage cartilage degradation. Matrix Biol. 2002, 21: 271-88. 10.1016/S0945-053X(02)00004-5.PubMed Little CB, Hughes CE, Curtis CL, Janusz MJ, Bohne R, Wang-Weigand S, Taiwo YO, Mitchell PG, Otterness IG, Flannery CR, Caterson B: Matrix metalloproteinases are involved in C-terminal and interglobular domain processing of cartilage aggrecan in late stage cartilage degradation. Matrix Biol. 2002, 21: 271-88. 10.1016/S0945-053X(02)00004-5.PubMed
91.
Zurück zum Zitat Fosang AJ, Last K, Stanton H, Weeks DB, Campbell IK, Hardingham TE, Hembry RM: Generation and novel distribution of matrix metalloproteinase-derived aggrecan fragments in porcine cartilage explants. J Biol Chem. 2000, 275: 33027-33037. 10.1074/jbc.M910207199.PubMed Fosang AJ, Last K, Stanton H, Weeks DB, Campbell IK, Hardingham TE, Hembry RM: Generation and novel distribution of matrix metalloproteinase-derived aggrecan fragments in porcine cartilage explants. J Biol Chem. 2000, 275: 33027-33037. 10.1074/jbc.M910207199.PubMed
92.
Zurück zum Zitat Stanton H, Fosang AJ: Matrix metalloproteinases are active following guanidine hydrochloride extraction of cartilage: generation of DIPEN neoepitope during dialysis. Matrix Biol. 2002, 21: 425-428. 10.1016/S0945-053X(02)00035-5.PubMed Stanton H, Fosang AJ: Matrix metalloproteinases are active following guanidine hydrochloride extraction of cartilage: generation of DIPEN neoepitope during dialysis. Matrix Biol. 2002, 21: 425-428. 10.1016/S0945-053X(02)00035-5.PubMed
93.
Zurück zum Zitat Sztrolovics R, White RJ, Roughley PJ, Mort JS: The mechanism of aggrecan release from cartilage differs with tissue origin and the agent used to stimulate catabolism. Biochem J. 2002, 362: 465-472. 10.1042/0264-6021:3620465.PubMedCentralPubMed Sztrolovics R, White RJ, Roughley PJ, Mort JS: The mechanism of aggrecan release from cartilage differs with tissue origin and the agent used to stimulate catabolism. Biochem J. 2002, 362: 465-472. 10.1042/0264-6021:3620465.PubMedCentralPubMed
94.
Zurück zum Zitat Lee ER, Lamplugh L, Davoli MA, Beauchemin A, Chan K, Mort JS, Leblond CP: Enzymes active in the areas undergoing cartilage resorption during the development of the secondary ossification center in the tibiae of rats ages 0–21 days: I. Two groups of proteinases cleave the core protein of aggrecan. Dev Dyn. 2001, 222: 52-70. 10.1002/dvdy.1168.PubMed Lee ER, Lamplugh L, Davoli MA, Beauchemin A, Chan K, Mort JS, Leblond CP: Enzymes active in the areas undergoing cartilage resorption during the development of the secondary ossification center in the tibiae of rats ages 0–21 days: I. Two groups of proteinases cleave the core protein of aggrecan. Dev Dyn. 2001, 222: 52-70. 10.1002/dvdy.1168.PubMed
95.
Zurück zum Zitat Maroudas A, Bayliss MT, Uchitel-Kaushansky N, Schneiderman R, Gilav E: Aggrecan turnover in human articular cartilage: use of aspartic acid racemization as a marker of molecular age. Arch Biochem Biophys. 1998, 350: 61-71. 10.1006/abbi.1997.0492.PubMed Maroudas A, Bayliss MT, Uchitel-Kaushansky N, Schneiderman R, Gilav E: Aggrecan turnover in human articular cartilage: use of aspartic acid racemization as a marker of molecular age. Arch Biochem Biophys. 1998, 350: 61-71. 10.1006/abbi.1997.0492.PubMed
96.
Zurück zum Zitat Sandy JD, Verscharen C: Analysis of aggrecan in human knee cartilage and synovial fluid indicates that aggrecanase (ADAMTS) activity is responsible for the catabolic turnover and loss of whole aggrecan whereas other protease activity is required for C-terminal processing in vivo. Biochem J. 2001, 358: 615-626. 10.1042/0264-6021:3580615.PubMedCentralPubMed Sandy JD, Verscharen C: Analysis of aggrecan in human knee cartilage and synovial fluid indicates that aggrecanase (ADAMTS) activity is responsible for the catabolic turnover and loss of whole aggrecan whereas other protease activity is required for C-terminal processing in vivo. Biochem J. 2001, 358: 615-626. 10.1042/0264-6021:3580615.PubMedCentralPubMed
97.
Zurück zum Zitat van Meurs JB, van Lent PL, Holthuysen AE, Singer II, Bayne EK, van den Berg WB: Kinetics of aggrecanase- and metalloproteinase-induced neoepitopes in various stages of cartilage destruction in murine arthritis. Arthritis Rheum. 1999, 42: 1128-1139. 10.1002/1529-0131(199906)42:6<1128::AID-ANR9>3.0.CO;2-2.PubMed van Meurs JB, van Lent PL, Holthuysen AE, Singer II, Bayne EK, van den Berg WB: Kinetics of aggrecanase- and metalloproteinase-induced neoepitopes in various stages of cartilage destruction in murine arthritis. Arthritis Rheum. 1999, 42: 1128-1139. 10.1002/1529-0131(199906)42:6<1128::AID-ANR9>3.0.CO;2-2.PubMed
98.
Zurück zum Zitat van Meurs J, van Lent P, Stoop R, Holthuysen A, Singer I, Bayne E, Mudgett J, Poole R, Billinghurst C, van der Kraan P, Buma P, van den Berg W: Cleavage of aggrecan at the Asn341-Phe342 site coincides with the initiation of collagen damage in murine antigen-induced arthritis: a pivotal role for stromelysin 1 in matrix metalloproteinase activity. Arthritis Rheum. 1999, 42: 2074-2084. 10.1002/1529-0131(199910)42:10<2074::AID-ANR7>3.0.CO;2-5.PubMed van Meurs J, van Lent P, Stoop R, Holthuysen A, Singer I, Bayne E, Mudgett J, Poole R, Billinghurst C, van der Kraan P, Buma P, van den Berg W: Cleavage of aggrecan at the Asn341-Phe342 site coincides with the initiation of collagen damage in murine antigen-induced arthritis: a pivotal role for stromelysin 1 in matrix metalloproteinase activity. Arthritis Rheum. 1999, 42: 2074-2084. 10.1002/1529-0131(199910)42:10<2074::AID-ANR7>3.0.CO;2-5.PubMed
99.
Zurück zum Zitat Mudgett JS, Hutchinson NI, Chartrain NA, Forsyth AJ, McDonnell J, Singer II, Bayne EK, Flanagan J, Kawka D, Shen CF, Stevens K, Chen H, Trumbauer M, Visco DM: Susceptibility of stromelysin 1-deficient mice to collagen-induced arthritis and cartilage destruction. Arthritis Rheum. 1998, 41: 110-121. 10.1002/1529-0131(199801)41:1<110::AID-ART14>3.3.CO;2-7.PubMed Mudgett JS, Hutchinson NI, Chartrain NA, Forsyth AJ, McDonnell J, Singer II, Bayne EK, Flanagan J, Kawka D, Shen CF, Stevens K, Chen H, Trumbauer M, Visco DM: Susceptibility of stromelysin 1-deficient mice to collagen-induced arthritis and cartilage destruction. Arthritis Rheum. 1998, 41: 110-121. 10.1002/1529-0131(199801)41:1<110::AID-ART14>3.3.CO;2-7.PubMed
100.
Zurück zum Zitat Mort JS, Magny MC, Lee ER: Cathepsin B: an alternative protease for the generation of an aggrecan 'metalloproteinase' cleavage neoepitope. Biochem J. 1998, 335: 491-494.PubMedCentralPubMed Mort JS, Magny MC, Lee ER: Cathepsin B: an alternative protease for the generation of an aggrecan 'metalloproteinase' cleavage neoepitope. Biochem J. 1998, 335: 491-494.PubMedCentralPubMed
101.
Zurück zum Zitat Mason RM, Chambers MG, Flannelly J, Gaffen JD, Dudhia J, Bayliss MT: The STR/ort mouse and its use as a model of osteoarthritis. Osteoarthritis Cartilage. 2001, 9: 85-91. 10.1053/joca.2000.0363.PubMed Mason RM, Chambers MG, Flannelly J, Gaffen JD, Dudhia J, Bayliss MT: The STR/ort mouse and its use as a model of osteoarthritis. Osteoarthritis Cartilage. 2001, 9: 85-91. 10.1053/joca.2000.0363.PubMed
102.
Zurück zum Zitat Chambers MG, Cox L, Chong L, Suri N, Cover P, Bayliss MT, Mason RM: Matrix metalloproteinases and aggrecanases cleave aggrecan in different zones of normal cartilage but colocalize in the development of osteoarthritic lesions in STR/ort mice. Arthritis Rheum. 2001, 44: 1455-1465. 10.1002/1529-0131(200106)44:6<1455::AID-ART241>3.0.CO;2-J.PubMed Chambers MG, Cox L, Chong L, Suri N, Cover P, Bayliss MT, Mason RM: Matrix metalloproteinases and aggrecanases cleave aggrecan in different zones of normal cartilage but colocalize in the development of osteoarthritic lesions in STR/ort mice. Arthritis Rheum. 2001, 44: 1455-1465. 10.1002/1529-0131(200106)44:6<1455::AID-ART241>3.0.CO;2-J.PubMed
103.
Zurück zum Zitat Sasaki M, Seo-Kiryu S, Kato R, Kita S, Kiyama H: A disintegrin and metalloprotease with thrombospondin type1 motifs (ADAMTS-1) and IL-1 receptor type 1 mRNAs are simultaneously induced in nerve injured motor neurons. Brain Res Mol Brain Res. 2001, 89: 158-163. 10.1016/S0169-328X(01)00046-8.PubMed Sasaki M, Seo-Kiryu S, Kato R, Kita S, Kiyama H: A disintegrin and metalloprotease with thrombospondin type1 motifs (ADAMTS-1) and IL-1 receptor type 1 mRNAs are simultaneously induced in nerve injured motor neurons. Brain Res Mol Brain Res. 2001, 89: 158-163. 10.1016/S0169-328X(01)00046-8.PubMed
104.
Zurück zum Zitat Singer II, Scott S, Kawka DW, Bayne EK, Weidner JR, Williams HR, Mumford RA, Lark MW, McDonnell J, Christen AJ, Moore VL, Mudgett JS, Visco DM: Aggrecanase and metalloproteinase-specific aggrecan neo-epitopes are induced in the articular cartilage of mice with collagen II-induced arthritis. Osteoarthritis Cartilage. 1997, 5: 407-418.PubMed Singer II, Scott S, Kawka DW, Bayne EK, Weidner JR, Williams HR, Mumford RA, Lark MW, McDonnell J, Christen AJ, Moore VL, Mudgett JS, Visco DM: Aggrecanase and metalloproteinase-specific aggrecan neo-epitopes are induced in the articular cartilage of mice with collagen II-induced arthritis. Osteoarthritis Cartilage. 1997, 5: 407-418.PubMed
105.
Zurück zum Zitat Lemons ML, Sandy JD, Anderson DK, Howland DR: Intact aggrecan and fragments generated by both aggrecanse and metalloproteinase-like activities are present in the developing and adult rat spinal cord and their relative abundance is altered by injury. J Neurosci. 2001, 21: 4772-4781.PubMed Lemons ML, Sandy JD, Anderson DK, Howland DR: Intact aggrecan and fragments generated by both aggrecanse and metalloproteinase-like activities are present in the developing and adult rat spinal cord and their relative abundance is altered by injury. J Neurosci. 2001, 21: 4772-4781.PubMed
106.
Zurück zum Zitat Satoh K, Suzuki N, Yokota H: ADAMTS-4 (a disintegrin and metalloproteinase with thrombospondin motifs) is transcriptionally induced in beta-amyloid treated rat astrocytes. Neurosci Lett. 2000, 289: 177-180. 10.1016/S0304-3940(00)01285-4.PubMed Satoh K, Suzuki N, Yokota H: ADAMTS-4 (a disintegrin and metalloproteinase with thrombospondin motifs) is transcriptionally induced in beta-amyloid treated rat astrocytes. Neurosci Lett. 2000, 289: 177-180. 10.1016/S0304-3940(00)01285-4.PubMed
107.
Zurück zum Zitat Konttinen YT, Mandelin J, Li TF, Salo J, Lassus J, Liljestrom M, Hukkanen M, Takagi M, Virtanen I, Santavirta S: Acidic cysteine endoproteinase cathepsin K in the degeneration of the superficial articular hyaline cartilage in osteoarthritis. Arthritis Rheum. 2002, 46: 953-960. 10.1002/art.10185.PubMed Konttinen YT, Mandelin J, Li TF, Salo J, Lassus J, Liljestrom M, Hukkanen M, Takagi M, Virtanen I, Santavirta S: Acidic cysteine endoproteinase cathepsin K in the degeneration of the superficial articular hyaline cartilage in osteoarthritis. Arthritis Rheum. 2002, 46: 953-960. 10.1002/art.10185.PubMed
108.
Zurück zum Zitat Lang A, Horler D, Baici A: The relative importance of cysteine peptidases in osteoarthritis. J Rheumatol. 2000, 27: 1970-1979.PubMed Lang A, Horler D, Baici A: The relative importance of cysteine peptidases in osteoarthritis. J Rheumatol. 2000, 27: 1970-1979.PubMed
Metadaten
Titel
Aggrecanases and cartilage matrix degradation
verfasst von
Hideaki Nagase
Masahide Kashiwagi
Publikationsdatum
01.03.2003
Verlag
BioMed Central
Erschienen in
Arthritis Research & Therapy / Ausgabe 2/2003
Elektronische ISSN: 1478-6362
DOI
https://doi.org/10.1186/ar630

Weitere Artikel der Ausgabe 2/2003

Arthritis Research & Therapy 2/2003 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.