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PMID: 4265022 Published · ppublish English Journal Article

Replacement of proteoglycans in embryonic chick cartilage in organ culture after treatment with testicular hyaluronidase.

The Biochemical journal ·Vol. 129 ·No. 1 ·1972-08-00 ·Pages 101-12

Hardingham TE, Fitton-Jackson S, Muir H

Abstract

Explants of cartilage from tibiae of 11-12 days chick embryos were grown in organ culture. To one group hyaluronidase was added to the medium during the first 2 days of culture; the treated tissue was then cultured in medium without enzyme for a further 4 days. Control explants grown in hyaluronidase-free medium for 6 days grew rapidly in size and the total hexosamine content more than doubled during this time. After exposure to hyaluronidase, much of the hexosamine was lost from treated cartilage and appeared in the culture medium, but it was mostly replaced in the tissue during the subsequent recovery period. Analysis of cartilage and medium showed that net synthesis of hexosamine increased greatly in treated cartilage. The proteoglycans were extracted by two procedures from control and treated cartilage after 2, 4 and 6 days in culture. The hydrodynamic sizes of the purified proteoglycans were compared by gel chromatography and the composition of the gel-chromatographic fractions was determined. The proteoglycans from controls did not change during culture, but after exposure to hyaluronidase the proteoglycans from treated cartilage were of much smaller size and lower chondroitin sulphate content. During recovery, even though new proteoglycans were formed, they were nevertheless of smaller size and lower chondroitin sulphate content than control proteoglycans. They gradually became more like control proteoglycans during recovery from treatment, but even after 4 days they were not yet the same. After 2 days of treatment with the enzyme, the chondroitin sulphate in the cartilage was of shorter chain length than in controls but during recovery after 4 and 6 days in culture, the chain lengths in control and treated cartilage were similar. It is concluded that the proteoglycans formed in embryo cartilage in response to their depletion by enzyme treatment contained fewer chondroitin sulphate chains attached to the protein moiety of proteoglycans. This may have resulted from a failure under stress to glycosylate the protein moiety to the usual extent; alternatively the synthesis of normal proteoglycans of low chondroitin sulphate content may have increased, thus changing the proteoglycan population.

MeSH Terms
Animals Cartilage/metabolism Chick Embryo Chondroitin/biosynthesis Chromatography DNA/analysis Glycosaminoglycans/analysis,biosynthesis Hexosamines/biosynthesis Hyaluronoglucosaminidase/pharmacology Male Organ Culture Techniques Testis/enzymology Uronic Acids/analysis
Chemicals
Glycosaminoglycans Hexosamines Uronic Acids Chondroitin DNA Hyaluronoglucosaminidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hardingham T E
Fitton-Jackson S
Muir H
References (27)
27 references, click to expand
  1. Method for the determination of hexosamines in tissues.
    J Biol Chem. 1953 Oct;204(2):553-63 PMID: 13117829
  2. Biosynthesis of proteoglycans in cartilage slices. Fractionation by gel chromatography and equilibrium density-gradient centrifugation.
    Biochem J. 1972 Feb;126(4):791-803 PMID: 4262896
  3. Reversible collapse of rabbit ears after intravenous papain, and prevention of recovery by cortisone.
    J Exp Med. 1956 Aug 1;104(2):245-52 PMID: 13345969
  4. The separation of new forms of the proteinpolysaccharides of bovine nasal cartilage.
    J Biol Chem. 1966 Sep 25;241(18):4261-6 PMID: 5924647
  5. Characterization of protein-polysaccharides of articular cartilage from mature and immature pigs.
    Biochem J. 1969 Oct;114(4):871-6 PMID: 4241960
  6. A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.
    Biochem J. 1956 Feb;62(2):315-23 PMID: 13293190
  7. A method for the determination of molecular weight dispersion in chondroitin sulphate on a microgram level.
    Biochim Biophys Acta. 1969 Feb 18;177(1):152-4 PMID: 5781188
  8. Heterogeneity of protein-polysaccharides of porcine articular cartilage. The chondroitin sulphate proteins associaterd with collagen.
    Biochem J. 1971 Aug;123(5):747-55 PMID: 4330908
  9. The release of chondroitin sulfate from rabbit cartilage following the intravenous injection of crude papain.
    Arch Biochem Biophys. 1958 Jul;76(1):122-30 PMID: 13560020
  10. The chemistry of connective tissues. 6. The constitution of the chondroitin sulphate-protein complex in cartilage.
    Biochem J. 1961 Apr;79:15-26 PMID: 13733048
  11. Environmental control of macromolecular synthesis in cartilage and bone: morphogenetic response to hyaluronidase.
    Proc R Soc Lond B Biol Sci. 1970 Sep 29;175(1041):405-53 PMID: 4393939
  12. Crystalline papain. I. Preparation, specificity, and activation.
    J Biol Chem. 1954 Apr;207(2):515-31 PMID: 13163037
  13. A modified uronic acid carbazole reaction.
    Anal Biochem. 1962 Oct;4:330-4 PMID: 13971270
  14. Hyaluronidases.
    Adv Enzymol Relat Subj Biochem. 1952;13:199-236 PMID: 14943668
  15. A comparison of proteinpolysaccharides of bovine nasal cartilage isolated and fractionated by different methods.
    J Biol Chem. 1970 Aug 25;245(16):4112-22 PMID: 4250552
  16. The proteinpolysaccharides of bovine nucleus pulposus.
    J Biol Chem. 1967 Oct 25;242(20):4691-701 PMID: 6061415
  17. Transglycosylation during the mixed digestion of hyaluronic acid and chondroitin sulfate by testicular hyaluronidase.
    J Biol Chem. 1956 Apr;219(2):653-63 PMID: 13319286
  18. Papain-induced changes in rabbit cartilage; alterations in the chemical structure of the cartilage matrix.
    J Exp Med. 1958 Oct 1;108(4):507-13 PMID: 13575681
  19. Proteinpolysaccharide complex from bovine nasal cartilage. A comparison of low and high shear extraction procedures.
    J Biol Chem. 1969 Jan 10;244(1):77-87 PMID: 4237578
  20. Sodium chondroitin sulfate-protein complexes of cartilage. I. Molecular weight and shape.
    Arch Biochem Biophys. 1958 Mar;74(1):158-74 PMID: 13522234
  21. Cellular control of macromolecular synthesis: rates of synthesis of extracellular macromolecules during and after depletion by papain.
    Proc R Soc Lond B Biol Sci. 1968 Mar 26;169(1017):399-425 PMID: 4384431
  22. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  23. Cartilage changes in papain-treated rabbits.
    Am J Pathol. 1957 Nov-Dec;33(6):1237-45 PMID: 13478667
  24. Studies on protein-polysaccharides from pig laryngeal cartilage. Heterogeneity, fractionation and characterization.
    Biochem J. 1969 Aug;113(5):885-94 PMID: 4241689
  25. POSSIBLE SYNTHESIS OF POLYRIBONUCLEOTIDES OF KNOWN BASE-TRIPLET SEQUENCES.
    Nature. 1965 Apr 3;206:93 PMID: 14334364
  26. THE ESTIMATION OF DEOXYRIBONUCLEIC ACID IN THE PRESENCE OF SIALIC ACID: APPLICATION TO ANALYSIS OF HUMAN GASTRIC WASHINGS.
    Biochem J. 1965 Jun;95:612-20 PMID: 14342494
  27. Proteoglycans of cartilage: an assessment of their structure.
    Biochim Biophys Acta. 1971 Feb 16;229(2):529-34 PMID: 5102885
Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1972-08-00
Pages
101-12
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1174046
Subset
IM
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