Skip to main content
Log in

Sequential Distribution of Keratan Sulphate and Chondroitin Sulphate Epitopes During Ameloblast Differentiation

  • Published:
The Histochemical Journal Aims and scope Submit manuscript

Abstract

Proteoglycans are complex macromolecules containing one or more glycosaminoglycan chains and exhibiting a variety of biological functions in connective tissues. The aim of the present study was to immunolocalize the distribution of keratan sulphate and chondroitin sulphate epitopes during initial enamel formation in order to study temporo-spatial expression patterns of these macromolecules. Third molars of four-months-old pigs were used for immunolocalization of keratan sulphate and chondroitin sulphate epitopes in the developing enamel layer. Tooth organs were prepared for paraffin sections in order to perform indirect immunohistochemistry. The results demonstrated a mutually exclusive positioning between these two epitopes. Keratan sulphate epitopes were observed in pre-secretory pre-ameloblasts and adjacent stratum intermedium while chondroitin sulphate epitopes were demonstrated in secretory ameloblasts and adjacent stratum intermedium. Our findings suggest that proteoglycans containing glycosaminoglycan chains may play a regulatory role during enamel mineralization.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References cited

  • Caterson B, Christner JE, Baker JR, Couchman JR (1985) Production and characterization of monoclonal antibodies directed against connective tissue proteoglycans. Fed Proc 44: 386-393.

    Google Scholar 

  • Chardin H, Septier D, Goldberg M (1990) Visualization of glycosaminoglycans in rat incisor predentin and dentin with cetylpyridinium chloride-glutaraldehyde as fixative. J Histochem Cytochem 38: 885-894.

    Google Scholar 

  • Cheng H, Caterson B, Neame PJ, Lester GE, Yamauchi M (1996) Differential distribution of lumican and fibromodulin in tooth cementum. Connect Tiss Res 34: 87-96.

    Google Scholar 

  • Diekwisch T, David S, Bringas P, Santos V, Slavkin HC (1993) Antisense inhibition of AMEL translation demonstrates supramolecular controls for enamel HAP crystal growth during embryonic mouse molar development. Development 117: 471-482.

    Google Scholar 

  • Diekwisch TGH, Ware J, Fincham AG, Zeichner-David M (1997) Immunohistochemical similarities and differences between amelogenin and tuftelin gene products during tooth development. J Histochem Cytochem 45: 859-866.

    Google Scholar 

  • Doi Y, Eanes ED, Shimokawa H, Termine JD (1984) Inhibition of seeded growth of enamel apatite crystals by amelogenin and enamelin protein in vitro. J Dent Res 58B: 98-105.

    Google Scholar 

  • Fincham AG, Lau EC, Simmer J, Zeichner-David M (1992) Amelogenin biochemistry — form and function. In: Slavkin HC, Price P, eds. Chemistry and Biology of Mineralized Tissues. Amsterdam: Excerpta Media, pp. 187-201.

    Google Scholar 

  • Frank RM, Osman M, Meyer JM, Ruch JV (1979) 3H-glucosamine electron microscope autoradiography after isolated labeling of the enamel organ or the dental papilla followed by reassociated toothgerm culture. J Biol Buccale 7: 225-241.

    Google Scholar 

  • Galbraith DB, Cutler LS, Kollar EJ (1992) The correlation of temporal regulation of glycosaminoglycan synthesis with morphogenetic events in mouse tooth development. Arch Oral Biol 37: 623-628.

    Google Scholar 

  • Goldberg M, Septier D (1986) Ultrastructural location of complex carbohydrates in developing rat incisor enamel. Anat Rec 216: 181-190.

    Google Scholar 

  • Goldberg M, Septier D (1992) Differential staining of glycosaminoglycans in the predentine and dentine of rat incisor using cuprolinic blue at various magnseium chloride concentrations. Histochem J 24: 648-654.

    Google Scholar 

  • Goldberg M, Lecolle S (1995) Poly-L-lysine-gold complexes used at different pH are probes for differential detection of glycosaminoglycans and phosphoproteins in the predentine and dentine of rat incisor. Histochem J 27: 401-410.

    Google Scholar 

  • Goldberg M, Septier D, Escaig-Haye F (1987) Glycoconjugates in deninogenesis and dentine. Prog Histochem Cytochem 17: 1-112.

    Google Scholar 

  • Goldberg M, Chardin H, Septier D, Lecolle S (1993) Proteoglycans—phospholipids interactions: roles in dentine mineralization. C R Seances Soc Biol Fil 187: 210-222.

    Google Scholar 

  • Heinegard D, Oldberg A (1993) Glycosylated matrix proteins. In: Royce PM, Steinmen B, eds. Connective Tissue and Its Heritable Disorders. New York: Wiley-Liss Inc., pp. 189-209.

    Google Scholar 

  • Hurmerinta K (1982) Autoradiographic visualization of glycoproteins and glycosaminoglycans in the epithelio-mesenchymal interface of developing mouse tooth germ. Scand J Dent Res 90: 278-285.

    Google Scholar 

  • Iozzo RV, Murdoch AD (1996) Proteoglycans of the extracellular environment: clues from the gene and protein side offer novel perspectives in molecular diversity and function. FASEB J 10: 598-614.

    Google Scholar 

  • Kakizawa Y, Kasuya K, Kojima N, Nagai S, Takagi H, Fukui K (1976) An histochemical study on acid mucopolysaccharides in the enameloid formation stages of fish (Oplegnathus fasciatus). J Nihon Univ Sch Dent 18: 105-113.

    Google Scholar 

  • Kogaya Y, Furuhashi K (1985) Ultrastructural distribution of acidic glycosaminoglycans associated with matrix vesicle-mediated calcification in mouse progenitor predentine. Calc Tiss Int 37: 36-41.

    Google Scholar 

  • Kogaya Y, Furuhashi K (1987) Ultrastructural distribution of sulfated glycosaminoglycans in epithelial—mesenchymal interface of developing rat tooth germs. J Histochem Cytochem 35: 585-593.

    Google Scholar 

  • Krebsbach PH, Lee SK, Matsuki Y, Kozak CA, Yamada RM, Yamada Y (1996) Full-length sequence, localization, and chromosomal mapping of ameloblastin — a novel tooth-specific gene. J Biol Chem 271: 4431-4435.

    Google Scholar 

  • Lau EC, Ruch JV (1983) Glycosaminoglycans in embryonic mouse teeth and the dissociated dental constituents. Differentiation 23: 234-242.

    Google Scholar 

  • Lau E, Arechaga J, Ruch JV (1983a) Glycosaminoglycans in embryonic mouse tooth germs. A histochemical analysis. J Biol Buccale 11: 23-34.

    Google Scholar 

  • Lau E, Boukari A, Arechaga J, Osman M, Ruch JV (1983b) [35S] autoradiographic study of sulfatedGAGaccumulation and turnover in embryonic mouse tooth germs. J Craniofac Genet Dev Biol 3: 117-131.

    Google Scholar 

  • Lander AD (1993) Proteoglycans. In: Thomas Kreis, Ronald Vale, eds. Guidebook to the Extracellular Matrix and Adhesion Proteins. Oxford: Oxford University Press. pp. 12-16.

    Google Scholar 

  • Laurie GW, Leblond CP, Martin GR (1982) Localization of type IV collagen, laminin, heparan sulfate proteoglycan, and fibronectin to the basal lamina of basement membranes. J Cell Biol 95: 340-344.

    Google Scholar 

  • Lormee P, Lecolle S, Septier D, Le Denmat D, Goldberg M (1989) Autometallography for histochemical visualization of rat incisor polyanions with cuprolinic blue. J Histochem Cytochem 37: 203-208.

    Google Scholar 

  • Lyngstadaas SP, Risnes S, Sproat BS, Thrane PS, Prydz HP (1996) A synthetic, chemically-modified ribozyme eliminates amelogenin, the major translation product in developing mouse enamel in vivo. EMBO J 14: 5224-5229.

    Google Scholar 

  • Mark MP, Baker JR, Kimata K, Ruch J-V (1990a) Regulated changes in chondroitin sulfation during embryogenesis: an immunohistochemical approach. Int J Dev Biol 34: 191-204.

    Google Scholar 

  • Mark MP, Baker JR, Morrison K, Ruch JV (1990b) Chondroitin sulfates in developing mouse tooth germs. An immunohistochemical study with monoclonal antibodies against chondroitin-4 and chondroitin-6 sulfates. Differentiation 43: 37-50.

    Google Scholar 

  • Mark MP, Zupan-Bloch A, Ruch JV (1992) Patterned distributions of chondroitin sulfate isoforms, retinoic acid receptor gamma and cellular retinoic acid binding proteins in the embryonic mouse incisor. Proc Finn Dent Soc 88: 439-449.

    Google Scholar 

  • Ruch JV (1985) Epithelial-mesenchymal interactions. In: Butler WT, ed. The Chemistry and Biology of Mineralized Tissues. Birmingham: EBSCO Media, pp. 54-61.

    Google Scholar 

  • Ruch JV, Lesot H, Karcher-Djuricic V, Meyer JM, Mark M (1983) Epithelial—mesenchymal interactions in tooth germs: mechanisms of differentiation. J Biol Buccale 11: 173-193.

    Google Scholar 

  • Sasagawa I (1995) Fine structure of tooth germs during the formation of enameloid matrix in Talapia nilotica, a teleost fish. Arch Oral Biol 40: 801-814.

    Google Scholar 

  • Sasagawa I (1997) Fine structure of the cap enameloid and of the dental epithelial cells during enameloid mineralization and early maturation stages in the tilapia, a teleost. J Anat 190: 589-600.

    Google Scholar 

  • Sasaki T (1990) Cell Biology of Tooth Enamel Formation. Basel, Switzerland: Karger, pp. 39-42.

    Google Scholar 

  • Slavkin HC, Brownell AG, Bringas P, MacDougall M, Bessem C (1983) Basal lamina persistance during epithelial—mesenchymal interactions in murine tooth development in vitro. J Craniofac Gen Dev Biol 3: 387-407.

    Google Scholar 

  • Thesleff I, Pratt RM (1980) Tunicamycin inhibits mouse tooth morphogenesis and odontoblast differentiation in vitro. J Embryol Exp Morphol 58: 195-208.

    Google Scholar 

  • Thesleff I, Stenman S, Vaheri A, Timpl R (1979) Changes in the matrix proteins, fibronectin and collagen, during differentiation of mouse tooth germ. Dev Biol 70: 116-126.

    Google Scholar 

  • Thesleff I, Partanen A-M, Vainio S (1991) Epithelial—mesenchymal interactions in tooth morphogenesis: The roles of extracellular matrix, growth factors, and cell surface receptors. J Craniofac Gen Dev Biol.

  • Warshawsky H, Moore G (1967) Atechnique for the fixation and decalcification of rat incisors for electron microscopy. J Histochem Cytochem 15: 542-549.

    Google Scholar 

  • Wight T, Heinegard DK, Hascall VC (1991) Proteoglycans. Structure and function. In: Hay ED, ed. Cell Biology of the Extracellular Matrix. New York: Plenum Press, pp. 45-78.

    Google Scholar 

  • Zeichner-David M, Vo H, Tan H, Diekwisch T, Berman B, Thiemann F, Alcocer MD, Hsu P, Wang T, Reyna J, Caton J, Slavkin HC, MacDougall M (1997) Timing of the expression of enamel gene products during mouse tooth development. Int J Dev Biol 41: 27-38.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Thieberg, R., Yamauchi, M., Satchell, P. et al. Sequential Distribution of Keratan Sulphate and Chondroitin Sulphate Epitopes During Ameloblast Differentiation. Histochem J 31, 573–578 (1999). https://doi.org/10.1023/A:1003871322914

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1003871322914

Keywords

Navigation