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. 1968 Oct 1;39(1):43–48. doi: 10.1083/jcb.39.1.43

EVIDENCE FOR CHANGES IN PROTEIN POLYSACCHARIDE ASSOCIATED WITH THE ONSET OF CALCIFICATION IN CARTILAGE

Victor J Matukas 1, George A Krikos 1
PMCID: PMC2107512  PMID: 5692685

Abstract

Past work has suggested that protein polysaccharide may play a role in the calcification of cartilage. Recent electron microscopic studies on noncalcified cartilage have indicated that protein polysaccharide in cartilage matrix is represented by granules associated with collagen fibers. The present work has been designed for comparison of the matrix of noncalcified cartilage to that of calcified cartilage, with particular reference to these granules. Small blocks of tibia from 16-day embryos were fixed in cacodylate-buffered glutaraldehyde and postfixed in either phosphate- or Veronal-buffered osmium tetroxide. Special care was taken to maintain the pH above 7.0 at all times. For electron microscopy the tissues were dehydrated, embedded in Epon 812, sectioned, and stained with uranyl acetate or lead citrate. A marked decrease in the size of granules in the matrix of calcified cartilage compared to noncalcified cartilage was noted. Associated with the decrease in the size of granules was a condensation of matrix components and the presence of an amorphous electron-opaque material that was not seen in noncalcified areas. These results are interpreted to represent either a drop in concentration or a change in state of protein polysaccharide with the onset of calcification in cartilage.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ANDERSON D. R. THE ULTRASTRUCTURE OF ELASTIC AND HYALINE CARTILAGE OF THE RAT. Am J Anat. 1964 May;114:403–434. doi: 10.1002/aja.1001140305. [DOI] [PubMed] [Google Scholar]
  2. Anderson H. C. Electron microscopic studies of induced cartilage development and calcification. J Cell Biol. 1967 Oct;35(1):81–101. doi: 10.1083/jcb.35.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. CAMERON D. A., ROBINSON R. A. Electron microscopy of cartilage and bone matrix at the distal epiphyseal line of the femur in the newborn infant. J Biophys Biochem Cytol. 1956 Jul 25;2(4 Suppl):253–260. doi: 10.1083/jcb.2.4.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CAMERON D. A. The fine structure of bone and calcified cartilage. A critical review of the contribution of electron microscopy to the understading of osteogenesis. Clin Orthop Relat Res. 1963;26:199–228. [PubMed] [Google Scholar]
  5. CAULFIELD J. B. Effects of varying the vehicle for OsO4 in tissue fixation. J Biophys Biochem Cytol. 1957 Sep 25;3(5):827–830. doi: 10.1083/jcb.3.5.827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Greenspan J. S., Blackwood H. J. Histochemical studies of chondrocyte function in the cartilage of the mandibular codyle of the rat. J Anat. 1966 Jul;100(Pt 3):615–626. [PMC free article] [PubMed] [Google Scholar]
  7. Hirschman A., Dziewiatkowski D. D. Protein-polysaccharide loss during endochondral ossification: immunochemical evidence. Science. 1966 Oct 21;154(3747):393–395. doi: 10.1126/science.154.3747.393. [DOI] [PubMed] [Google Scholar]
  8. LUCY J. A., DINGLE J. T., FELL H. B. Studies on the mode of action of excess of vitamin A. 2. A possible role of intracellular proteases in the degradation of cartilage matrix. Biochem J. 1961 Jun;79:500–508. doi: 10.1042/bj0790500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lindenbaum A., Kuettner K. E. Mucopolysaccharides and mucoproteins of calf scapula. Calcif Tissue Res. 1967;1(2):153–165. doi: 10.1007/BF02008085. [DOI] [PubMed] [Google Scholar]
  11. Matukas V. J., Panner B. J., Orbison J. L. Studies on ultrastructural identification and distribution of protein-polysaccharide in cartilage matrix. J Cell Biol. 1967 Feb;32(2):365–377. doi: 10.1083/jcb.32.2.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. PALADE G. E. A study of fixation for electron microscopy. J Exp Med. 1952 Mar;95(3):285–298. doi: 10.1084/jem.95.3.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. ROBINSON R. A., CAMERON D. A. The organic matrix of bone and epiphyseal cartilage. Clin Orthop. 1957;9:16–29. [PubMed] [Google Scholar]
  15. SCOTT B. L., PEASE D. C. Electron microscopy of the epiphyseal apparatus. Anat Rec. 1956 Dec;126(4):465–495. doi: 10.1002/ar.1091260405. [DOI] [PubMed] [Google Scholar]
  16. TAKUMA S. Electron microscopy of the developing cartilagenous epiphysis. Arch Oral Biol. 1960 Jul;2:111–119. doi: 10.1016/0003-9969(60)90059-5. [DOI] [PubMed] [Google Scholar]
  17. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]

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