Specific properties of the extracellular chondroitin sulphate proteoglycans in the mandibular condylar growth centre in pigs

Archives of Oral Biology

Volumn 42, Issue 1, 1997, Pages 63-76

  Roth, S ^a   Muller K ^a   Fischer, D C ^b   Dannhauer, K H ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Aggrecan; Antibodies; Cartilage; Fibrous tissue; Growth; Proteoglycans; Temporomandibular joint; Versican

Indexed keywords

AGGRECAN; KERATAN SULFATE; PROTEOCHONDROITIN SULFATE; PROTEOGLYCAN; SCLEROPROTEIN; VERSICAN;

ANIMAL; ANIMAL TISSUE; ARTICLE; ARTICULAR CARTILAGE; CELL DIFFERENTIATION; CELL PROLIFERATION; CHEMISTRY; CHONDROGENESIS; COMPARATIVE STUDY; DEGLYCOSYLATION; DENSITY GRADIENT CENTRIFUGATION; EXTRACELLULAR MATRIX; FEMUR HEAD; GROWTH PLATE; GROWTH, DEVELOPMENT AND AGING; IMMUNOHISTOCHEMISTRY; ISOLATION AND PURIFICATION; MANDIBLE CONDYLE; MOLECULAR WEIGHT; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; SWINE; TEMPOROMANDIBULAR JOINT; TISSUE DISTRIBUTION;

ANIMALIA; SUS SCROFA; SUS SCROFA DOMESTICA;

EID: 0343196700     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-9969(97)83718-1     Document Type: Article

References (62)

1. Barry F. P., Gaw J. U., Young C. N. and Neame P. J. (1992) Hyaluronan-binding region of aggrecan from pig laryngeal cartilage. Biochem J. 286, 761-769.
2. Ben-Ami D., von der Mark K., Franzen A., Bernard B., Lunazzi G. C. and Silbermann M. (1993) Transformation of fetal secondary cartilage into embryonic bone in organ cultures of human mandibular condyles. Conn. Tiss. Res. 271, 317-322.
3. Blackwood H. J. J. (1966) Growth of mandibular condyle of the rat studied with tritiated thymidine. Archs oral Biol. 11, 493-500.
4. Bradford M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analyt. Biochem. 12, 248-254.
5. Bratt P., Anderson M. M., Mansson-Rahemtulla B., Stevens J. W., Zhou C. and Rahemtulla F. (1992) Isolation and characterization of bovine gingival proteoglycans versican and decorin. Int. J. Biochem. 24, 1573-1583.
6. Caplan A. I. (1984) Cartilage. Sci. Am. 251, 84-94.
7. Chandrasekaran L. and Tanzer M. (1992) Molecular cloning of chicken aggrecan. Biochem. J. 288, 903-910.
8. Copray J. C. V. M. and Jansen H. W. B. (1985) Cyclic nucleotides and growth regulation of the mandibular condylar cartilage of the rat in vitro. Archs oral Biol. 30, 749-752.
9. Dannhauer K.-H. (1992) Die Wachstumsreaktion des mandibulären Gelenkknorpels auf biomechanische Reize und ihre Bedeutung für die Funktionskieferorthopädie. Fortschr. Kieferorthop. 53, 53-60.
10. Doege K., Sasaki M., Horigan E., Hassell J. R. and Yamada Y. (1987) Complete primary structure of the rat cartilage proteoglycan core protein deduced for cDNA clones. J. biol. Chem. 262, 17757-17767.
11. Doege K., Sasaki M., Kimura T. and Yamada Y. (1991) Complete coding sequence and deduced primary structure of the human cartilage large aggregating proteoglycan, aggrecan. J. biol. Chem. 266, 894-902.
12. Durkin J. F., Heeley J. D. and Irving J. T. (1985) Der Knorpel des Kondylus. In Physiologie und Pathologie des Kiefergelenks (Eds Zarb G. A. and Carlsson G. E.), pp. 49-113. Quintessenz, Berlin.
13. Dziewiatkowski D. D., LaValley J. and Beaudoin A. G. (1989) Age-related changes in the composition of proteoglycans in sheep cartilages. Conn. Tiss. Res. 19, 103-120.
14. Farndale R. W., Buttle D. S. and Barrett A. S. (1986) Improved quantitation and discrimination of sulphated glucosaminoglycans by use of dimethylene blue. Biochim. Biophys. Acta 883, 173-177.
15. Fischer D.-C., Kolbe-Busch S., Stöcker G., Hoffman A. and Haubeck H.-D. (1994) Development of enzyme immunoassays specific for keratan sulphate-and core-protein-epitopes of the large aggregating proteoglycan from human articular cartilaee. Er. J. clin. Chem. clin. Biochem. 32, 285-291.
16. Giant T. T., Mikecz K., Roughley P. J., Buzas E. and Poole A. R. (1986) Age related changes in protein related epitopes of human articular cartilage proteoglycans. Biochem. J. 236, 71-75.
17. Goetinck P. F. (1982) Proteoglycans in developing embryonic cartilage. In The Glycoconjugates (Ed. Horowitz M. J.), pp. 197-229. Academic Press, New York..
18. Grover J. and Roughley P. J. (1993) Versican gene expression in human articular cartilage and comparison of mRNA splicing variation with aggrecan. Biochem. J. 291, 361-367.
19. Hardingham T. E. and Fosang A. J. (1992) Proteoglycans: many forms, many functions. Faseb. J. 6, 861-870.
20. Hardingham T. E., Fosang A. J. and Dudhia J. (1992) Aggrecan. the chondroitin sulfate keratan sulfate proteoglycan from cartilage. In Articular Cartilage and Osteoarthritis (Eds Kuettner K. E., Schleyerbach R. S., Peyron J. G. and Hascall V. C.), pp. 5-19. Raven, New York..
21. Hardingham T. E., Fosang A. J. and Dudhia J. (1994) The structure, function and turnover of aggrecan, the large aggregating proteoglycan from cartilage. Eur. J. clin. Chem. clin. Biochem. 32, 249-257.
22. Hay E. D. (1991) Cell Biology of Extracellular Matrix (Ed Hay E. D.). Plenum, New York..
23. Heinegård D. (1972) Extraction, fractionation and characterization of proteoglycans from bovine tracheal cartilage. Biochim. Biophys. Acta 285, 181-192.
24. Heinegård D. (1977) Polydispersity of proteoglycans. Structural variations with size and buoyant density of the molecules. J. biol. Chem. 252, 1980-1989.
25. Heinegård D., Björne-Persson A., Cöster L., Franzen A., Gardell S., Malmström A., Paulsson M., Sandfalk R. and Vogel K. (1985) The core proteins of large and small proteoglycans from various connective tissues form distinct subgroups. Biochem. J. 230, 181-194.
26. Heinegård D., Lorenzo P., Reinholt F. P. and Sommarin Y. (1993) Aging and the extracellular matrix. In Musculoskeletal Soft-tissue Aging: Impact on Mobility (Eds Buckwalter S. A., Goldberg V. M. and Wood S. L.-Y.), pp. 349-361. American Academy of Orthopaedic Surgeons, New York.
27. Heinegård D., Paulsson M., Inerot S. and Carlström C. (1981) A novel low-molecular weight chondroitin sulphate proteoglycan isolated from cartilage. Biochem. J. 197, 355-366.
28. Ilie M. Z., Handley C. J., Robinson H. C. and Mok M. T. (1992) Mechanism of catabolism of aggrecan by articular cartilage. Archs Biochem. Biophys. 294, 115-122.
29. Ito K., Shinomura T., Zako M., Ujita M. and Kimata K. (1995) Multiple forms of mouse PG-M, a large chondroitin sulfate proteoglycan generated by alternative splicing. J. biol. Chem. 270, 958-965.
30. 2+ in mandibular condylar growth and adaptation. Am. J. Orthod. Dentofac. Orthop. 99, 418-426.
31. Kantomaa T., Pirttiniemi P., Tuominen M. and Poelka A. (1994a) Glycosaminoglycan synthesis in the mandibular condyle during growth adaptation. Acta Anat. 151, 88-96.
32. Kantomaa T., Toummen M. and Pirttiniemi P. (1994b) Effect of mechanical forces on chondrocyte maturation and differentiation in the mandibular condyle of the rat. J. dent. Rex. 73, 1150-1156.
33. Kielty C., Hopkinson I. and Grant M. E. (1993) Collagen: the collagen family: Structure, assembly, and organization in the extracellular matrix. In Connective Tissue and its Heritable Disorders (Eds Royce M. P. and Steinmann B.), pp. 103 147. Wiley-Liss, London..
34. Kimata K., Oike Y., Tani K., Shinomura T., Yamagata M., Uritani M. and Suzuki SW. (1986) A large chondroitin sulfate proteoglycan (PG-M) synthesized before chondrogenesis in the limb bud of chick embryo. J. biol. Chem. 261, 13517-13525.
35. Kjellen L. and Lindahl U. (1991) Proteoglycans: structure and interactions. Annu. Rev. Biochem. 60, 443-475.
36. Kuettner K. E. (1992) Biochemistry of articular cartilage in health and disease. Clin. Biochem. 25, 155-163.
37. Laemmli U. K. (1970) Cleavage of structural proteins during assembly of the head of bacteriophage T4. Nature 227, 680-685.
38. Landesberg R. L., Proctor R. L., Rosier R. N. and Puzas J. E. (1995) The mandibular condylar growth center: separation and characterization of the cellular elements. Calcif. Tissue Int. 56, 71-77.
39. Langille R. M. (1994) Chondrogenic differentiation in cultures of embryonic rat mesenchyme. Micr. Res. Techn. 28, 455-469.
40. Lewandowska K., Choi H. L., Rosenberg L. C., Zardi L. and Culp L. A. (1987) Fibronectin-mediated adhesion of fibroblasts: inhibition by dermatan-sulfate proteoglycan and evidence for a cryptic glycosaminoglycan-binding domain. J. Cell. Biol. 105, 443-454.
41. Maor G., Laron Z. and Silbermann M. (1993) The early postnatal development in the murine mandibular condyle is regulated by endogenous insulin-like growth factor-I. J. Endocrinol. 137, 21-26.
42. Moss M. L. (1960) Functional analysis of human mandibular growth. J. Proth. Dent. 10, 1149-1153.
43. Nishida Y., Shinomura T., Iwata H., Miura T. and Kimata K. (1994) Abnormal occurrence of a large chondroitin sulfate proteoglycan PG-M versican in osteoarthritic cartilage. Osteoarthr. Cartil. 2, 43-49.
44. Petrovic A. and Stutzmann J. (1986) The concept of the mandibular tissue-level growth potential and the responsiveness to a functional appliance. Orthodontics: State of the Art, Essence of the Science (Ed. Graber-Lee W.). pp. 59-74. Mosby, St Louis.
45. Petrovic A. G. (1984) Experimental and cybernetic approaches to the mechanism of action of functional appliances on mandibular growth. In Malocclusioit and the Periodontium (Eds McNamara J. A. and Ribbens K. A.), pp. 213-268. Craniofacial Growth Series. Monograph 15, Center for Human Growth and Development, University of Michigan, Ann Arbor.
46. Roughley P. J. and Lee E. R. (1994) Cartilage proteoglycans: structure and potential functions. Micr. Res. Techn. 28, 385-397.
47. Roughley P. J. and White R. J. (1980) Age related changes in the structure of the proteoglycan subunits from human articular cartilage. J. biol. Chem. 255, 217-224.
48. Ruoshlati E. (1989) Proteoglycans in cell regulation. J. biol. Chem. 264, 13369-13372.
49. Shinomura T., Nishida Y. and Kimata K. (1992) A large chondroitin sulfate proteoglycan (PG-M) and cartilage differentiation. In Articular Cartilage and Osteoarthritis (Eds Kuettner K. E., Schleyerbach R. S., Peyron J. G. and Hascall, V. C.), pp. 35-43. Raven, New York.
50. Shinomura T. Y., Nishida Y., Ito K. and Kimata K. (1993) CDNA cloning of PG-M, a large chondroitin sulfate proteoglycan expressed during chondrogenesis in chick limb buds. J. biol. Chem. 268, 14461-14469.
51. Stutzmann J. and Petrovic A. (1979) Intrinsic regulation of condylar cartilage growth rate. Er. J. Orthod. 1, 41-54.
52. Urban J., Maroudas A., Bayliss M. T. and Dillon J. (1979) Swelling pressure of proteoglycans at the concentrations found in cartilaginous tissues. Biorheology 16, 447-464.
53. Urban J. P. G., Hall A. C. and Gehl K. A. (1993) Regulation of matrix synthesis rates by the ionic and osmotic environment of articular chondrocytes. J. Cell Physiol. 154, 262-270.
54. Vilim V. and Fosang A. J. (1994) Proteoglycans isolated from dissociative extracts of differently aged human articular cartilage: characterization of naturally occurring hyaluronan-binding fragments of aggrecan. Biocheni. J. 304, 887-894.
55. Walcz E., Desk F., Erhardt P., Coulter S. N., Fülöp C., Horvath P., Doege K. J. and Glant T. T. (1994) Complete coding sequence, deduced primary structure, chromosomal localization, and structural analysis of murine aggrecan. Genome 22, 364-371.
56. Webber C., Giant T. T., Roughley P. J. and Poole A. R. (1987) The identification and characterization of two populations of aggregating proteoglycans of high buoyant density isolated from post-natal human articular cartilage of different ages. Biochem. J. 248, 735-740.
57. Yamagata M. and Kimata K., (1994) Repression of a malignant cell-substrate adhesion phenotype by inhibiting the production of the anti-adhesive proteoglycan, PG-M/versican. J. Cell Sci. 107, 2581-2590.
58. Yamagata M., Saga S., Kato M., Bernfield M. and Kimata K. (1993a) Selective distributions of proteoglycans and their ligands in pericellular matrix of cultured fibroblasts. J. Cell Sci. 106, 55-65.
59. Yamagata M., Shinomura T. and Kimata K. (1993b) Tissue variation of two large chondroitin sulfate proteoglycans (PG-M versican and PG-H aggrecan) in chick embryos. Anat. Embryol. 187, 433-444.
60. Yamagata M., Suzuki S., Akiyama S., Yamada K. M. and Kimata K. (1989) Regulation of cell-substrate adhesion by proteoglycans immobilized on extracellular substrata. J. biol. Chem. 264, 8012-8018.
61. Zimmermann D. R., Dours-Zimmermann M. T., Schubert M. and Bruckner-Tudermann L. (1994) Versican is expressed in the proliferating zone in the epidermis and in association with elastic network of the dermis. J. Cell Biol. 124, 817-825.
62. Zimmermann D. R. and Ruoshlati E. (1989) Multiple domains of the large fibroblasts proteoglycan, versican. EMBO J. 8, 2975-2981.