Literature DB >> 10415722

Aggrecanase. A target for the design of inhibitors of cartilage degradation.

E C Arner1, M A Pratta, C P Decicco, C B Xue, R C Newton, J M Trzaskos, R L Magolda, M D Tortorella.   

Abstract

In arthritic diseases there is a gradual erosion of cartilage that leads to a loss of joint function. Aggrecan, which provides cartilage with its properties of compressibility and elasticity, is the first matrix component to undergo measurable loss in arthritis. This loss of aggrecan appears to be due to an increased rate of degradation, that can be attributed to proteolytic cleavage of the core protein within the interglobular domain (IGD). Two major sites of cleavage have been identified within the IGD. One, between the amino acids Asn341-Phe342, where the matrix metalloproteinases (MMPs) have been shown to clip; and the other, between Glu373-Ala374, which is attributed to a novel protease, "aggrecanase." We have generated aggrecanase in conditioned media from IL-1-stimulated bovine nasal cartilage and have used an enzymatic assay to evaluate this proteinase activity. In these studies we follow the generation of aggrecanase and MMPs in response to IL-1 in this system and examine the contribution of these enzymes in aggrecan degredation. Our data suggest that aggrecanase is a key enzyme in cartilage aggrecan degradation that represents a novel target for cartilage protection therapy in arthritis.

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Year:  1999        PMID: 10415722     DOI: 10.1111/j.1749-6632.1999.tb07676.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  14 in total

1.  Selective and non-selective metalloproteinase inhibitors reduce IL-1-induced cartilage degradation and loss of mechanical properties.

Authors:  Christopher G Wilson; Ashley W Palmer; Fengrong Zuo; Elsie Eugui; Stacy Wilson; Rebecca Mackenzie; John D Sandy; Marc E Levenston
Journal:  Matrix Biol       Date:  2006-11-11       Impact factor: 11.583

2.  [Histopathological degeneration score of fibrous cartilage. Low- and high-grade meniscal degeneration].

Authors:  V Krenn; B Kurz; M G Krukemeyer; P Knoess; M Jakobs; C Poremba; G Möllenhoff
Journal:  Z Rheumatol       Date:  2010-09       Impact factor: 1.372

3.  Esculetin inhibits cartilage resorption induced by interleukin 1alpha in combination with oncostatin M.

Authors:  S Elliott; A D Rowan; S Carrère; P Koshy; J B Catterall; T E Cawston
Journal:  Ann Rheum Dis       Date:  2001-02       Impact factor: 19.103

4.  Characterization of the human ADAMTS-5 (aggrecanase-2) gene promoter.

Authors:  Kannan Thirunavukkarasu; Yong Pei; Tao Wei
Journal:  Mol Biol Rep       Date:  2007-01-09       Impact factor: 2.316

5.  [Meniscal degeneration score and NITEGE expression : immunohistochemical detection of NITEGE in advanced meniscal degeneration].

Authors:  V Krenn; P Knöss; W Rüther; M Jakobs; M Otto; M G Krukemeyer; A Heine; G Möllenhoff; B Kurz
Journal:  Orthopade       Date:  2010-05       Impact factor: 1.087

6.  Perinatal exposure to vitamin A differentially regulates chondrocyte growth and the expression of aggrecan and matrix metalloprotein genes in the femur of neonatal rats.

Authors:  Yao Zhang; Amanda E Wray; A Catharine Ross
Journal:  J Nutr       Date:  2012-02-22       Impact factor: 4.798

7.  ADAMTS9 activation by interleukin 1 beta via NFATc1 in OUMS-27 chondrosarcoma cells and in human chondrocytes.

Authors:  Kursat Oguz Yaykasli; Toshitaka Oohashi; Satoshi Hirohata; Omer Faruk Hatipoglu; Kiichi Inagawa; Kadir Demircan; Yoshifumi Ninomiya
Journal:  Mol Cell Biochem       Date:  2008-12-04       Impact factor: 3.396

8.  Retinoic acid and the transcription factor MafB act together and differentially to regulate aggrecan and matrix metalloproteinase gene expression in neonatal chondrocytes.

Authors:  Yao Zhang; A Catharine Ross
Journal:  J Cell Biochem       Date:  2013-02       Impact factor: 4.429

9.  Tumor necrosis factor alpha-dependent aggrecan cleavage and release of glycosaminoglycans in the meniscus is mediated by nitrous oxide-independent aggrecanase activity in vitro.

Authors:  Henning Voigt; Angelika K Lemke; Rolf Mentlein; Michael Schünke; Bodo Kurz
Journal:  Arthritis Res Ther       Date:  2009-09-24       Impact factor: 5.156

10.  Cell-penetrating peptides released from thermosensitive nanoparticles suppress pro-inflammatory cytokine response by specifically targeting inflamed cartilage explants.

Authors:  Rush L Bartlett; Shaili Sharma; Alyssa Panitch
Journal:  Nanomedicine       Date:  2012-10-03       Impact factor: 5.307

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