Literature DB >> 208518

The simultaneous release by bone explants in culture and the parallel activation of procollagenase and of a latent neutral proteinase that degrades cartilage proteoglycans and denatured collagen.

G Vaes, Y Eeckhout, G Lenaers-Claeys, C François-Gillet, J E Druetz.   

Abstract

1. A latent neutral proteinase was found in culture media of mouse bone explants. Its accumulation during the cultures is closely parallel to that of procollagenase; both require the presence of heparin in the media. 2. Latent neutral proteinase was activated by several treatments of the media known to activate procollagenase, such as limited proteolysis by trypsin, chymotrypsin, plasmin or kallikrein, dialysis against 3 M-NaSCN at 4 degrees C and prolonged preincubation at 25 degrees C. Its activation often followed that of the procollagenase present in the same media. 3. Activation of neutral proteinase (as does that of procollagenase) by trypsin or plasmin involved two successive steps: the activation of a latent endogenous activator present in the media followed by the activation of neutral proteinase itself by that activator. 4. The proteinase degrades cartilage proteoglycans, denatured collagen (Azocoll) and casein at neutral pH; it is inhibited by EDTA, cysteine or serum. Collagenase is not inhibited by casein or Azocoll and is less resistant to heat or to trypsin than is the proteinase. Partial separation of the two enzymes was achieved by gel filtration of the media but not by fractional (NH4)2SO4 precipitation, by ion exchange or by affinity chromatography on Sepharose-collagen. These fractionations did not activate latent enzymes. 5. Trypsin activation decreases the molecular weight of both latent enzymes (60 000-70 000) by 20 000-30 000, as determined by gel filtration of media after removal of heparin. 6. The latency of both enzymes could be due either to a zymogen or to an enzyme-inhibitor complex. A thermostable inhibitor of both enzymes was found in some media. However, combinations of either enzyme with that inhibitor were not reactivated by trypsin, indicating that this inhibitor is unlikely to be the cause of the latency.

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Year:  1978        PMID: 208518      PMCID: PMC1185692          DOI: 10.1042/bj1720261

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  31 in total

1.  Evidence that latent collagenases are enzyme-inhibitor complexes.

Authors:  A Sellers; E Cartwright; G Murphy; J J Reynolds
Journal:  Biochem J       Date:  1977-05-01       Impact factor: 3.857

2.  Synthesis and secretion by rabbit bone-marrow macrophages in culture of a neutral proteinase that degrades cartilage proteoglycans [proceedings].

Authors:  P Hauser; G Vaes
Journal:  Biochem Soc Trans       Date:  1977       Impact factor: 5.407

3.  Metalloproteases of human articular cartilage that digest cartilage proteoglycan at neutral and acid pH.

Authors:  A I Sapolsky; H Keiser; D S Howell; J F Woessner
Journal:  J Clin Invest       Date:  1976-10       Impact factor: 14.808

4.  Comparative biochemistry of chondroitin sulphate-proteins of cartilage and notochord.

Authors:  M B Mathews
Journal:  Biochem J       Date:  1971-11       Impact factor: 3.857

5.  Degradation of cartilage proteoglycans by a neutral proteinase secreted by rabbit bone-marrow macrophages in culture.

Authors:  P Hauser; G Vaes
Journal:  Biochem J       Date:  1978-05-15       Impact factor: 3.857

6.  The secretion of enzymes into the pericellular environment.

Authors:  J T Dingle
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1975-07-17       Impact factor: 6.237

7.  Procollagenase from bovine gingiva.

Authors:  H Birkedal-Hansen; C M Cobb; R E Taylor; H M Fullmer
Journal:  Biochim Biophys Acta       Date:  1976-03-11

8.  Action of degradative enzymes on the light fraction of bovine septa protein polysaccharide.

Authors:  M Luscombe; C F Phelps
Journal:  Biochem J       Date:  1967-04       Impact factor: 3.857

9.  A collagenolytic system produced by primary cultures of rheumatoid nodule tissue.

Authors:  E D Harris
Journal:  J Clin Invest       Date:  1972-11       Impact factor: 14.808

10.  On the mechanisms of bone resorption. The action of parathyroid hormone on the excretion and synthesis of lysosomal enzymes and on the extracellular release of acid by bone cells.

Authors:  G Vaes
Journal:  J Cell Biol       Date:  1968-12       Impact factor: 10.539

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  15 in total

1.  Lipocytes from normal rat liver release a neutral metalloproteinase that degrades basement membrane (type IV) collagen.

Authors:  M J Arthur; S L Friedman; F J Roll; D M Bissell
Journal:  J Clin Invest       Date:  1989-10       Impact factor: 14.808

2.  The precursor of a metalloendopeptidase from human rheumatoid synovial fibroblasts. Purification and mechanisms of activation by endopeptidases and 4-aminophenylmercuric acetate.

Authors:  Y Okada; E D Harris; H Nagase
Journal:  Biochem J       Date:  1988-09-15       Impact factor: 3.857

3.  Type-I collagen production by human odontoblast-like cells in explants cultured on cyanoacrylate films. Electron-immunolocalization of fibronectin at cell/film interface.

Authors:  H Magloire; A Callé; D J Hartmann; A Joffre; B Serre; J A Grimaud; F Schué
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

4.  Degradation of basement membranes by human matrix metalloproteinase 3 (stromelysin).

Authors:  P A Bejarano; M E Noelken; K Suzuki; B G Hudson; H Nagase
Journal:  Biochem J       Date:  1988-12-01       Impact factor: 3.857

5.  Zinc metalloenzyme properties of active and latent collagenase from rabbit bone.

Authors:  J C Swann; J J Reynolds; W A Galloway
Journal:  Biochem J       Date:  1981-04-01       Impact factor: 3.857

Review 6.  Cell-to-cell interactions in the secretion of enzymes of connective tissue breakdown, collagenase and proteoglycan-degrading neutral proteases. A review.

Authors:  G Vaes
Journal:  Agents Actions       Date:  1980-12

7.  Purification and characterization of a rabbit bone metalloproteinase that degrades proteoglycan and other connective-tissue components.

Authors:  W A Galloway; G Murphy; J D Sandy; J Gavrilovic; T E Cawston; J J Reynolds
Journal:  Biochem J       Date:  1983-03-01       Impact factor: 3.857

8.  Biosynthesis and secretion of procollagenase by rabbit synovial fibroblasts. Inhibition of procollagenase secretion by monensin and evidence for glycosylation of procollagenase.

Authors:  H Nagase; C E Brinckerhoff; C A Vater; E D Harris
Journal:  Biochem J       Date:  1983-08-15       Impact factor: 3.857

9.  The extraction of a neutral metalloproteinase from the involuting rat uterus, and its action on cartilage proteoglycan.

Authors:  A Sellers; J F Woessner
Journal:  Biochem J       Date:  1980-09-01       Impact factor: 3.857

10.  A direct simultaneous plate assay of proteoglycan and collagen degradation by cells in culture and its application to synovial cells.

Authors:  C Peeters-Joris; X Emonds-Alt; G Vaes
Journal:  Biochem J       Date:  1981-04-15       Impact factor: 3.857

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