Literature DB >> 6245866

Macrophage factor that induces neutral protease secretion by normal rabbit chondrocytes. Studies of some properties and effects on metabolism of chondrocytes.

K Deshmukh-Phadke, S Nanda, K Lee.   

Abstract

Normal rabbit-articular chondrocytes secrete very small amounts of degradative enzymes in culture. Rabbit peritoneal macrophages, when activated with lipopolysaccharides, release a factor in the medium which stimulates the chondrocytes to produce significantly high levels of collagenase and other neutral protease for 2-3 days. The soluble mediator from macrophages appears to be a polypeptide with a molecular weight of 13000-15000 and can be inactivated by short-term treatment with trypsin or pronase. The enzyme-synthesis by chondrocytes can be stimulated to the same extent by repeated addition of the macrophage-medium. The metabolism of chondrocytes is altered due to the presence of this mediator. The cellular proliferation is diminished, while the rates of degradation as well as biosynthesis of the matrix are increased. These studies suggest the possibility that in the conditions such as osteoarthritis, where the synovial cells may not play an active role in cartilage degradation, the proteases can be produced by the cartilage cells themselves after the stimulation by macrophage-derived mediators. These intrinsic enzymes may be responsible for the slow, but progressive degeneration of cartilage tissue.

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Year:  1980        PMID: 6245866     DOI: 10.1111/j.1432-1033.1980.tb04413.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  15 in total

1.  Intracellular catabolin-like activity in cultured synovial tissue.

Authors:  J T Dingle; E Qi
Journal:  In Vitro       Date:  1983-12

2.  Influence of macrophage products on the release of plasminogen activator, collagenase, beta-glucuronidase and prostaglandin E2 by articular chondrocytes.

Authors:  V Evêquoz; J Schnyder; U Trechsel; M Baggiolini; H Fleisch
Journal:  Biochem J       Date:  1984-04-15       Impact factor: 3.857

Review 3.  Cytokine modulation of chondrocyte metabolism--in vivo and in vitro effects of piroxicam.

Authors:  J H Herman; A M Appel; R C Khosla; K S Kelch; E V Hess
Journal:  Inflammation       Date:  1984-06       Impact factor: 4.092

4.  Secretion of chondrocyte stimulating factor by macrophages as a result of activation with collagen and proteoglycans.

Authors:  K Phadke; S Nanda
Journal:  Clin Exp Immunol       Date:  1983-03       Impact factor: 4.330

5.  Light and electron microscopy of corneal melting syndrome (Mooren's ulcer).

Authors:  R D Young; P G Watson
Journal:  Br J Ophthalmol       Date:  1982-06       Impact factor: 4.638

6.  Matrix depletion of young and old human articular cartilage by cultured autologous synovium fragments: a chondrocyte-independent effect.

Authors:  A A Dogterom; O Huber-Bruning; J E Vernooy; B Wilbrink; W den Otter; J Huber
Journal:  Rheumatol Int       Date:  1985       Impact factor: 2.631

7.  Recombinant human interleukin-1 alpha and recombinant human interleukin-1 beta stimulate cartilage matrix degradation and inhibit glycosaminoglycan synthesis.

Authors:  R J Smith; N A Rohloff; L M Sam; J M Justen; M R Deibel; J C Cornette
Journal:  Inflammation       Date:  1989-08       Impact factor: 4.092

8.  Human mononuclear cell factors mediate cartilage matrix degradation through chondrocyte activation.

Authors:  H E Jasin; J T Dingle
Journal:  J Clin Invest       Date:  1981-09       Impact factor: 14.808

9.  Lymphocytes induce resorption of cartilage by producing catabolin.

Authors:  J Saklatvala; S J Sarsfield
Journal:  Biochem J       Date:  1982-01-15       Impact factor: 3.857

10.  Characterization of proteins from human synovium and mononuclear leucocytes that induce resorption of cartilage proteoglycan in vitro.

Authors:  J Saklatvala; S J Sarsfield; L M Pilsworth
Journal:  Biochem J       Date:  1983-02-01       Impact factor: 3.857

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