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Alcian Blue staining of glycosaminoglycans in embryonic material: Effect of different fixatives

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Summary

Glycosaminoglycans are important components of the extracellular matrix of developing embryos where they are found in the form of proteoglycans. Alcian Blue staining of tissue sections is the technique most commonly used for demonstrating their distribution. Glycosaminoglycans have a high solubility in water, and are easily lost from the tissue during processing, even if non-aqueous fixatives have been used. Formalin and Carnoy's fluid are the most frequently used fixatives, and the addition of cetyl pyridinium chloride has been recommended to reduce glycan solubility.

Using sections of day-10 rat embryos containing developing head and heart (both known to be rich in glycosaminoglycans) the effects of ten fixatives have been investigated with and without cetyl pyridinium chloride on the preservation of Alcian Blue-stainable material (at pH 2.5) and tissue structure. The most useful fixatives were Karnovsky's and Sainte-Marie's. Both gave a strong and reproducible staining pattern of the extracellular polyanionic material. Sainte-Marie's gave better preservation of tissue structure, allowing the demonstration of cell-matrix inter-relationships; Karnovsky's gave a better contrast between extracellular and intracellular staining, which is particularly useful at lower magnifications.

Cetyl pyridinium chloride is a detergent. Transmission electron microscope observations showed that it causes cell membrane disruption and vesicle formation, which at the light microscopic level, would cause cell membrane-associated glycosaminoglycans to appear as stained strands wholly within the extracellular domain. Therefore the use of cetyl pyridinium chloride is inadvisable where a distinction between surface-related and extracellular glycosaminoglycans is desirable. It has the further disadvantage of enhancing cytoplasmic and nuclear polyanionic material, thus decreasing the differential staining intensity of intracellular and extracellular domains.

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References

  • BARD, J. B. L. & ABBOTT, A. S. (1979) Matrices containing glycosaminoglycans in the developing anterior chambers of chick andXenopus embryonic eyes.Devl. Biol. 68, 472–86.

    Google Scholar 

  • BERNFIELD, M. R. & BANERJEE, S. D. (1972) Acid mucopolysaccharide (glycosaminoglycan) at the epithelial—mesenchymal interface of mouse embryo salivary glands.J. Cell Biol. 52, 664–73.

    Google Scholar 

  • BERNFIELD, M. R., BANERJEE, S. D., KODA, J. E. & RAPRAEGER, A. C. (1984) Remodeling of the basement membrane as a mechanism of morphogenetic tissue interaction. InThe role of Extracellular Matrix in Development (edited by TRELSTAD, R. L.) pp. 545–72. New York: Alan R. Liss Inc.

    Google Scholar 

  • CAMPBELL, M. A., BROWN, K. S., HASSELL, J. R., HORIGAN, E. A. & KEELER, R. F. (1985) Inhibition of limb chondrogenesis by aVeratum alkaloid: Temporal specificityin vivo andin vitro.Devl. Biol. 111, 464–70.

    Google Scholar 

  • COUCHMAN, J. R., CATERSON, B., CHRISTNER, J. E. & BAKER, J. R. (1984) Mapping by monoclonal antibody detection of glycosaminoglycan in connective tissues.Nature 307, 650–2.

    Google Scholar 

  • DERBY, M. A. (1978) Analysis of glycosaminoglycan within the extracellular environments encountered by migrating neural crest cells.Devl. Biol. 66, 321–36.

    Google Scholar 

  • DERBY, M. A. & PINTAR, J. E. (1978) The histochemical specificity ofStreptomyces hyaluronidase and chondroitinase ABC.Histochem. J. 10, 529–47.

    Google Scholar 

  • ENGFELDT, B. & HJERTQUIST, S.-O. (1976) The effect of various fixatives on the preservation of acid glycosaminoglycans in tissues.Acta pathol. microbiol. Scand. 71, 219–32.

    Google Scholar 

  • GALLAGHER, B. C. (1986) Basal laminar thinning in branching morphogenesis of the chick lung as demonstrated by lectin probes.J. Embryol. exp. Morphol. 94, 173–88.

    Google Scholar 

  • GIRARD, N., DELPECH, A. & DELPECH, B. (1986) Characterization of hyaluronic acid on tissue sections with hyaluronectin.J. Histochem. Cytochem. 34, 539–42.

    Google Scholar 

  • GOLDSTEIN, C. D., JANKIEWICZ, J. J. & DESMOND, M. E. (1986) Identification of glycosaminoglycans in the chondrocranium of the chick embryo before and at the onset of chondrogenesis.J. Embryol. exp. Morphol. 93, 29–49.

    Google Scholar 

  • GURR, G. T. (1963)Biological Staining Methods, 7th edn. London: G. T. Gurr.

    Google Scholar 

  • HAYAT, M. A. (1970)Principles and Techniques of Electron Microscopy. Biological Applications, Vol. 1. New York: Van Nostrand Reinhold.

    Google Scholar 

  • KELLY, J. W., BLOOM, G. D. & SCOTT, J. E. (1963) Quarternary ammonium compounds in connective tissue histochemistry: I Selective unblocking.J. Histochem. Cytochem. 11, 791–7.

    Google Scholar 

  • KUPCHELLA, C. E., MATSOUKA, L. Y., BRYAN, B., WORTSMAN, J. & DIETRICH, J. G. (1984) Histochemical evaluation of glycosaminoglycan deposition in the skin.J. Histochem. Cytochem. 32, 1121–4.

    Google Scholar 

  • LUFT, J. H. (1971) Ruthenium red and violet. 1 Chemistry, purification, methods of use for electron microscopy and mechanism of action.Anat. Rec. 171, 347–68.

    Google Scholar 

  • MARKWALD, R. R., FITZHARRIS, T. P., BANK, H. & BERNANKE, D. H. (1978) Structural analyses on the matrical organization of glycosaminoglycans in developing endocardial cushion.Devl. Biol. 62, 292–316.

    Google Scholar 

  • MASAMUNE, H. & OSAKI, S.-J. (1943) Biochemical studies on carbohydrates. LXIX. Preparation of pure chondroitin sulfuric acid.Tokyo J. Exp. Med. 45, 121–7.

    Google Scholar 

  • MORRISS, G. M. & SOLURSH, M. (1978a) Regional differences in mesenchymal cell morphology and glycosaminoglycans in early neural-fold stage rat embryos.J. Embryol. exp. Morphol. 46, 37–52.

    Google Scholar 

  • MORRISS, G. M. & SOLURSH, M. (1978b) The role of primary mesenchyme in normal and abnormal morphogenesis of mammalian neural folds.Zoon 6, 33–8.

    Google Scholar 

  • MORRISS-KAY, G. M. & CRUTCH, B. (1982) Culture of rat embryos with β-D-xyloside: evidence of a role for proteoglycans in neurulation.J. Anat. 134, 491–506.

    Google Scholar 

  • MORRISS-KAY, G. M., TUCKETT, F. & SOLURSH, M. (1986) The effects ofStreptomyces hyaluronidase on tissue organization and cell cycle time in rat embryos.J. Embryol. exp. Morphol. 98, 50–70.

    Google Scholar 

  • O'CONNELL, J. J. & LOW, F. N. (1970) A histochemical and fine structural study of early extracellular connective tissue in the chick embryo.Anat. Rec. 167, 425–38.

    Google Scholar 

  • PEARSE, A. G. E. (1968)Histochemistry: Theoretical and Applied, 3rd edn. London: Churchill Livingstone.

    Google Scholar 

  • POUSTY, I., BARI-KHAN, M. A. & BUTLER, W. F. (1975) Leaching of glycosaminoglycans from tissue by the fixatives formalin—saline and formalin—centrimide.Histochemistry 7, 361–5.

    Google Scholar 

  • PRATT, R. M., LARSEN, M. A. & JOHNSTON, M. C. (1975) Migration of neural crest cells in a cell-free hyaluronaterich matrix.Devl. Biol. 74, 298–305.

    Google Scholar 

  • RAPRAEGER, A., JALKANEN, M. & BERNFIELD, M. (1986) Cell surface proteoglycan associates with the cytoskeleton at the basolateral cell surface of mouse mammary epithelial cells.J. Cell. Biol. 103, 2683–96.

    Google Scholar 

  • SABATINI, D. D., BENSCH, K. & BARRNETT, R. J. (1963) The preservation of cellular ultrastructure and enzymatic activity by aldehyde formation.J. Cell Biol. 17, 19–58.

    Google Scholar 

  • SCOTT, J. E. (1960) Aliphatic ammonium salts in the assay of acidic mucopolysaccharides from tissues.Meth. biochem. Anal. 8, 145–97.

    Google Scholar 

  • SCOTT, J. E. & DORLING, J. (1965) Differential staining of acid glycosaminoglycans (mucopolysaccharides) by Alcian Blue in salt solutions.Histochemie 5, 221–33.

    Google Scholar 

  • SILBERSTEIN, G. B. & DANIAL, C. W. (1982) Glycosaminoglycans in the basal lamina and extracellular matrix of the mouse mammary duct.Devl. Biol. 90, 215–22.

    Google Scholar 

  • STEEDMAN, H. F. (1950) Alcian blue 8GS: A new stain for mucin.Q. J. Microbiol. Sci. 91, 477–9.

    Google Scholar 

  • STERNBERG, J. & KIMBER, S. J. (1986) Distribution of fibronectin, laminin and entactin in the environment of migrating neural crest cells in early mouse embryos.J. Embryol. exp. Morphol. 91, 267–82.

    Google Scholar 

  • SZIRAMI, J. A. (1963) Quantitative approaches in the histochemistry of mucopolysaccharides.J. Histochem. Cytochem. 11, 24–43.

    Google Scholar 

  • TOOLE, B. P. (1981) Glycosaminoglycans in morphogenesis. InCell Biology of the Extracellular Matrix (edited by HAY, E. D.), chapter 9, pp. 259–94. New York: Plenum Press.

    Google Scholar 

  • TUCKETT, F. & MORRISS-KAY, G. M. (1988) The role of heparan sulphate proteoglycan during the period of cranial neurulation: evidence from heparitinase treatment of rat embryos. In preparation.

  • WOODS, A., HOOK, M., KJELLEN, L., SMITH, C. G. & REES, D. A. (1984) Relationship of heparan sulfate proteoglycans to the cytoskeleton and extracellular matrix of cultured fibroblasts.J. Cell. Biol. 99, 1743–53.

    Google Scholar 

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Tuckett, F., Morriss-Kay, G. Alcian Blue staining of glycosaminoglycans in embryonic material: Effect of different fixatives. Histochem J 20, 174–182 (1988). https://doi.org/10.1007/BF01746681

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