Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1986 Jan 15;233(2):357–367. doi: 10.1042/bj2330357

Quantitative analysis of type X-collagen biosynthesis by embryonic-chick sternal cartilage.

S A Jimenez, R Yankowski, A M Reginato
PMCID: PMC1153036  PMID: 3954741

Abstract

We have performed a quantitative analysis of the various collagens biosynthesized by organ cultures of whole embryonic-chick sternum and its separate anatomical regions corresponding to the zones of permanent hyaline and presumptive-calcification cartilages. Our studies demonstrated that embryonic-chick sternum devotes a large portion of its biosynthetic commitment towards production of Type X collagen, which represented approx. 18% of the total newly synthesized collagen. Comparison of the collagens biosynthesized by the permanent hyaline cartilage and by the cartilage from the presumptive-calcification zone demonstrated that Type X-collagen production was strictly confined to the presumptive-calcification region. Sequential extraction of the newly synthesized Type X collagen demonstrated the existence of two separate populations. One population (approx. 20%) was composed of easily extractable molecules that were solubilized with 1.0 m-NaCl/50 mM-Tris/HCI buffer, pH 7.4. The second population was composed of molecules that were not extractable even after repeated pepsin digestion, but became completely solubilized after treatment with 20 mM-dithiothreitol/0.15 M-NaCl buffer at neutral pH. These results suggest that most of the Type X collagen normally exists in the tissue as part of a pepsin-resistant molecular aggregate that may be stabilized by disulphide bonds. Quantitative analysis of the proportion of Type X collagen relative to the other collagens synthesized in the cultures indicated that this collagen was a major biosynthetic product of the presumptive-calcification cartilage, since it represented about 35% of the total collagen synthesized by this tissue. In contrast, the permanent hyaline cartilage did not display any detectable synthesis of Type X collagen. When compared on a per-cell basis, the chondrocytes from the presumptive-calcification zone synthesized approx. 33% more Type X collagen than the amount of Type II collagen synthesized by the chondrocytes from the permanent-hyaline-cartilage zone. Subsequently, it was demonstrated that Type X collagen is a structural component of chick sternum matrix, since quantitative amounts could be extracted from the region of presumptive calcification of 17-day-old chick-embryo sterna and from the calcified portion of adult-chick sterna. The strict topographic distribution in the expression of Type X collagen biosynthesis to the zone of presumptive calcification suggests that this collagen may play an important role in initiation or progression of tissue calcification.

Full text

PDF
357

Images in this article

Selected References

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

  1. Ayad S., Abedin M. Z., Grundy S. M., Weiss J. B. Isolation and characterisation of an unusual collagen from hyaline cartilage and intervertebral disc. FEBS Lett. 1981 Jan 26;123(2):195–199. doi: 10.1016/0014-5793(81)80286-4. [DOI] [PubMed] [Google Scholar]
  2. Benya P. D., Shaffer J. D. Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels. Cell. 1982 Aug;30(1):215–224. doi: 10.1016/0092-8674(82)90027-7. [DOI] [PubMed] [Google Scholar]
  3. Benya P. D. Two-dimensional CNBr peptide patterns of collagen types I, II and III. Coll Relat Res. 1981;1(1):17–26. doi: 10.1016/s0174-173x(80)80004-5. [DOI] [PubMed] [Google Scholar]
  4. Bruckner P., Mayne R., Tuderman L. p-HMW-collagen, a minor collagen obtained from chick embryo cartilage without proteolytic treatment of the tissue. Eur J Biochem. 1983 Nov 2;136(2):333–339. doi: 10.1111/j.1432-1033.1983.tb07746.x. [DOI] [PubMed] [Google Scholar]
  5. Burgeson R. E., Hebda P. A., Morris N. P., Hollister D. W. Human cartilage collagens. Comparison of cartilage collagens with human type V collagen. J Biol Chem. 1982 Jul 10;257(13):7852–7856. [PubMed] [Google Scholar]
  6. Burgeson R. E., Hollister D. W. Collagen heterogeneity in human cartilage: identification of several new collagen chains. Biochem Biophys Res Commun. 1979 Apr 27;87(4):1124–1131. doi: 10.1016/s0006-291x(79)80024-8. [DOI] [PubMed] [Google Scholar]
  7. Capasso O., Tajana G., Cancedda R. Location of 64K collagen producer chondrocytes in developing chicken embryo tibiae. Mol Cell Biol. 1984 Jun;4(6):1163–1168. doi: 10.1128/mcb.4.6.1163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Duance V. C., Wotton S. F., Voyle C. A., Bailey A. J. Isolation and characterization of the precursor of type M collagen. Biochem J. 1984 Aug 1;221(3):885–889. doi: 10.1042/bj2210885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gibson G. J., Beaumont B. W., Flint M. H. Synthesis of a low molecular weight collagen by chondrocytes from the presumptive calcification region of the embryonic chick sterna: the influence of culture with collagen gels. J Cell Biol. 1984 Jul;99(1 Pt 1):208–216. doi: 10.1083/jcb.99.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gibson G. J., Kielty C. M., Garner C., Schor S. L., Grant M. E. Identification and partial characterization of three low-molecular-weight collagenous polypeptides synthesized by chondrocytes cultured within collagen gels in the absence and in the presence of fibronectin. Biochem J. 1983 May 1;211(2):417–426. doi: 10.1042/bj2110417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gibson G. J., Schor S. L., Grant M. E. Effects of matrix macromolecules on chondrocyte gene expression: synthesis of a low molecular weight collagen species by cells cultured within collagen gels. J Cell Biol. 1982 Jun;93(3):767–774. doi: 10.1083/jcb.93.3.767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jimenez S. A., Bashey R. I. Solubilization of bovine heart-value collagen. Biochem J. 1978 Jul 1;173(1):337–340. doi: 10.1042/bj1730337. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Juva K., Prockop D. J. Modified procedure for the assay of H-3-or C-14-labeled hydroxyproline. Anal Biochem. 1966 Apr;15(1):77–83. doi: 10.1016/0003-2697(66)90249-1. [DOI] [PubMed] [Google Scholar]
  14. Kielty C. M., Hulmes D. J., Schor S. L., Grant M. E. Embryonic chick cartilage collagens. Differences in the low-Mr species present in sternal cartilage and tibiotarsal articular cartilage. FEBS Lett. 1984 Apr 24;169(2):179–184. doi: 10.1016/0014-5793(84)80314-2. [DOI] [PubMed] [Google Scholar]
  15. Kielty C. M., Kwan A. P., Holmes D. F., Schor S. L., Grant M. E. Type X collagen, a product of hypertrophic chondrocytes. Biochem J. 1985 Apr 15;227(2):545–554. doi: 10.1042/bj2270545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ninomiya Y., Olsen B. R. Synthesis and characterization of cDNA encoding a cartilage-specific short collagen. Proc Natl Acad Sci U S A. 1984 May;81(10):3014–3018. doi: 10.1073/pnas.81.10.3014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Reese C. A., Wiedemann H., Kühn K., Mayne R. Characterization of a highly soluble collagenous molecule isolated from chicken hyaline cartilage. Biochemistry. 1982 Mar 2;21(5):826–830. doi: 10.1021/bi00534a002. [DOI] [PubMed] [Google Scholar]
  18. Remington M. C., Bashey R. I., Brighton C. T., Jimenez S. A. Biosynthesis of a disulphide-bonded short-chain collagen by calf growth-plate cartilage. Biochem J. 1984 Nov 15;224(1):227–233. doi: 10.1042/bj2240227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Remington M. C., Bashey R. I., Brighton C. T., Jimenez S. A. Biosynthesis of a low molecular weight collagen by rabbit growth plate cartilage organ cultures. Coll Relat Res. 1983 May;3(3):271–277. doi: 10.1016/s0174-173x(83)80009-0. [DOI] [PubMed] [Google Scholar]
  20. Ricard-Blum S., Hartmann D. J., Herbage D., Payen-Meyran C., Ville G. Biochemical properties and immunolocalization of minor collagens in foetal calf cartilage. FEBS Lett. 1982 Sep 20;146(2):343–347. doi: 10.1016/0014-5793(82)80949-6. [DOI] [PubMed] [Google Scholar]
  21. Schmid T. M., Conrad H. E. A unique low molecular weight collagen secreted by cultured chick embryo chondrocytes. J Biol Chem. 1982 Oct 25;257(20):12444–12450. [PubMed] [Google Scholar]
  22. Schmid T. M., Conrad H. E. Metabolism of low molecular weight collagen by chondrocytes obtained from histologically distinct zones of the chick embryo tibiotarsus. J Biol Chem. 1982 Oct 25;257(20):12451–12457. [PubMed] [Google Scholar]
  23. Schmid T. M., Linsenmayer T. F. A short chain (pro)collagen from aged endochondral chondrocytes. Biochemical characterization. J Biol Chem. 1983 Aug 10;258(15):9504–9509. [PubMed] [Google Scholar]
  24. Schmid T. M., Linsenmayer T. F. Developmental acquisition of type X collagen in the embryonic chick tibiotarsus. Dev Biol. 1985 Feb;107(2):373–381. doi: 10.1016/0012-1606(85)90319-7. [DOI] [PubMed] [Google Scholar]
  25. Shimokomaki M., Duance V. C., Bailey A. J. Identification of a new disulphide bonded collagen from cartilage. FEBS Lett. 1980 Nov 17;121(1):51–54. doi: 10.1016/0014-5793(80)81265-8. [DOI] [PubMed] [Google Scholar]
  26. Strawich E., Nimni M. E. Properties of a collagen molecule containing three identical components extracted from bovine articular cartilage. Biochemistry. 1971 Oct 12;10(21):3905–3911. doi: 10.1021/bi00797a017. [DOI] [PubMed] [Google Scholar]
  27. Sussman M. D., Ogle R. C., Balian G. Biosynthesis and processing of collagens in different cartilaginous tissues. J Orthop Res. 1984;2(2):134–142. doi: 10.1002/jor.1100020204. [DOI] [PubMed] [Google Scholar]
  28. Yasui N., Benya P. D., Nimni M. E. Identification of a large interrupted helical domain of disulfide-bonded cartilage collagen. J Biol Chem. 1984 Nov 25;259(22):14175–14179. [PubMed] [Google Scholar]
  29. Yoshimura M., Jimenez S. A., Kaji A. Effects of viral transformation on synthesis and secretion of collagen and fibronectin-like molecules by embryonic chick chondrocytes in culture. J Biol Chem. 1981 Sep 10;256(17):9111–9117. [PubMed] [Google Scholar]
  30. van der Rest M., Mayne R., Ninomiya Y., Seidah N. G., Chretien M., Olsen B. R. The structure of type IX collagen. J Biol Chem. 1985 Jan 10;260(1):220–225. [PubMed] [Google Scholar]
  31. von der Mark K., van Menxel M., Wiedemann H. Isolation and characterization of a precursor form of M collagen from embryonic chicken cartilage. Eur J Biochem. 1984 Feb 1;138(3):629–633. doi: 10.1111/j.1432-1033.1984.tb07961.x. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES