Literature DB >> 1260491

The capacity of pig articular cartilage in organ culture to regenerate after breakdown induced by complement-sufficient antiserum to pig erythrocytes.

H B Fell, M E Barratt, H Welland, R Green.   

Abstract

Explants of pig articular cartilage including invading marrow and subchondral bone (together='invasion zone') were cultivated for 10 or 14 days in complement-sufficient rabbit antiserum to pig erythrocytes (AS+C'), and then transferred to heat-inactivated normal rabbit serum (NRS) for a period of recovery. In AS+C' the cartilage matrix lost first proteoglycan and then collagen, but the cells remained viable. The degradation of collagen was accompanied by a fibroblastic transformation of the chodrocytes, first seen in the region immediately above the invasion zone. Immunohistochemical studies showed that after cultivation in AS+C', IgG antibodies entered areas in which the matrix was depleted of proteoglycan and reacted strongly with the majority of chondrocytes; those that had under-gone fibroblastic transformation exhibited little or no reaction. The degree of recovery in NRS depended on the extent to which the matrix had broken down in AS+C'. If degradation of collagen was confined to the region immediately above the invasion zone, and elsewhere only proteoglycan had been lost, new metachromatic material was regenerated in the non-calcified cartilage, and the fibroblast-like chondrocytes resumed their normal appearance and regained their reactivity with the IgG antibodies of AS; new cartilage and chondroid tissue appeared in the cavities of the invasion zone. If degradation of collagen and fibroblastic transformation of chondrocytes had spread throughout the cartilage, breakdown continued in NRS and cartilage disappeared completely above the invasion zone; new cartilage waw sometimes formed in the cavities of the invasione zone.

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Year:  1976        PMID: 1260491     DOI: 10.1007/BF02546393

Source DB:  PubMed          Journal:  Calcif Tissue Res        ISSN: 0008-0594


  16 in total

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Authors:  J W LANDELLS
Journal:  J Bone Joint Surg Br       Date:  1957-08

2.  THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS IN VITRO, I. DEDIFFERENTIATION OF CARTILAGE CELLS.

Authors:  H Holtzer; J Abbott; J Lash; S Holtzer
Journal:  Proc Natl Acad Sci U S A       Date:  1960-12       Impact factor: 11.205

3.  The role of soft connective tissue in the breakdown of pig articular cartilage cultivated in the presence of complement-sufficient antiserum to pig erythrocytes. I. Histological changes.

Authors:  H B Fell; M E Barratt
Journal:  Int Arch Allergy Appl Immunol       Date:  1973

4.  Repair of the joint surface from subarticular tissue in the rabbit knee.

Authors:  G Meachim; C Roberts
Journal:  J Anat       Date:  1971-07       Impact factor: 2.610

5.  Role of the chondrocytes in the breakdown of pig articular cartilage induced by complement-sufficient antiserum to pig erythrocytes.

Authors:  M E Barratt
Journal:  Int Arch Allergy Appl Immunol       Date:  1975

6.  The breakdown of embryonic (chick) cartilage and bone cultivated in the presence of complement-sufficient antiserum. I. Morphological changes, their reversibility and inhibition.

Authors:  H B Fell; R R Coombs; J T Dingle
Journal:  Int Arch Allergy Appl Immunol       Date:  1966

7.  The loss of phenotypic traits by differentiated cells. IV. Changes in polysaccharides produced by dividing chondrocytes.

Authors:  M Nameroff; H Holtzer
Journal:  Dev Biol       Date:  1967-09       Impact factor: 3.582

8.  The loss of phenotypic traits by differentiated cells. 3. The reversible behavior of chondrocytes in primary cultures.

Authors:  J Abbott; H Holtzer
Journal:  J Cell Biol       Date:  1966-03       Impact factor: 10.539

9.  The role of soft connective tissue in the response of pig articular cartilage in organ culture to excess of retinol.

Authors:  M E Barratt
Journal:  J Cell Sci       Date:  1973-07       Impact factor: 5.285

10.  The loss of phenotypic traits by differentiated cells. VI. Behavior of the progeny of a single chondrocyte.

Authors:  S Chacko; J Abbott; S Holtzer; H Holtzer
Journal:  J Exp Med       Date:  1969-08-01       Impact factor: 14.307

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  9 in total

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Authors:  G R Dodge; A R Poole
Journal:  J Clin Invest       Date:  1989-02       Impact factor: 14.808

2.  Heberden oration 1978. Recent studies on the control of joint damage: the contribution of the Strangeways Research Laboratory.

Authors:  J T Dingle
Journal:  Ann Rheum Dis       Date:  1979-06       Impact factor: 19.103

3.  Effects of anti-inflammatory drugs on cartilage recovery from catabolin-induced degradation.

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4.  Inhibition of bovine nasal cartilage degradation by selective matrix metalloproteinase inhibitors.

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Journal:  Biochem J       Date:  1997-04-15       Impact factor: 3.857

5.  Inverse correlation between tyrosine phosphorylation and collagenase production in chondrocytes.

Authors:  T F Cruz; G Mills; K P Pritzker; R A Kandel
Journal:  Biochem J       Date:  1990-08-01       Impact factor: 3.857

Review 6.  The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders.

Authors:  S Elliott; T Cawston
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7.  Cathepsin B in osteoarthritis: cytochemical and histochemical analysis of human femoral head cartilage.

Authors:  A Baici; A Lang; D Hörler; R Kissling; C Merlin
Journal:  Ann Rheum Dis       Date:  1995-04       Impact factor: 19.103

Review 8.  Targeting Dysregulation of Metalloproteinase Activity in Osteoarthritis.

Authors:  Kazuhiro Yamamoto; David Wilkinson; George Bou-Gharios
Journal:  Calcif Tissue Int       Date:  2020-08-09       Impact factor: 4.333

Review 9.  Proteases involved in cartilage matrix degradation in osteoarthritis.

Authors:  Linda Troeberg; Hideaki Nagase
Journal:  Biochim Biophys Acta       Date:  2011-07-08
  9 in total

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