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Application of selected cationic dyes for the semiquantitative estimation of glycosaminoglycans in histological sections of articular cartilage by microspectrophotometry

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Summary

Selected commonly used cationic dyes, viz. Thionin, Safranin O, Toluidine Blue O, Dimethylmethylene Blue, Cuprolinic Blue, Cupromeronic Blue,N, N′-Diethylpseudoisocyanine, and a modified PAS-method, and staining method, with a variety of alternative procedures, e.g., variation of pH, use of the critical electrolyte concentration method, and blocking reactions (methylation-saponification, carboxymethylation), were tested to select optimal staining procedures for the semiquantitative histochemical estimation of glycosaminoglycans by microspectrophotometry in sections of articular cartilage. The methods were carried out on 3 μm-thick paraffin and 1 μm-thick glycolmethacrylate sections of bovine articular cartilage. The staining intensity of the sections was measured from spots 25 μm apart using a leitz MPV 3 microspectrophotometer, starting at the surface of the cartilage and ending up at the tidemark. The result was compared with the fixed-charge density graph determined from the adjacent articular cartilage.

Of the dyes tested, Thionin and Safranin O proved to be excellent cationic dyes for the histochemical quantification of cartilage matrix proteoglycans, since the staining intensity curves showed a linear correlation (r=0.900–0.995) with the fixed charge density curves from the adjacent cartilage. Also, the stain distribution was consistently uniform across the sections. In 1 μm-thick glycolmethacrylate sections, the Safranin O staining gradient showed almost perfect identity with the fixed-charge density curve. Cuprolinic Blue and Cupromeronic Blue combined with the critical electrolyte concentration technique were also useful for the microspectrophotometric assays of glycosaminoglycans, but the presence of metachromasia should be checked prior to the measurements. The reliability of blocking procedures for quantitative histochemical work was not convincing.

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References

  • Balázs, E. &Szirmai, J. (1958a) Dyebinding and mucopolysaccharide content in connective tissue.J. Histochem. Cytochem. 6, 416–24.

    PubMed  Google Scholar 

  • Balázs, E. &Szirmai, J. (1958b) Quantitative determination of cationic dyebinding in connective tissue.J. Histochem. Cytochem. 6, 278–89.

    PubMed  Google Scholar 

  • Bayliss, M., Venn, M., Maroudas, A. &Ali, S. (1983) Structure of proteoglycans from different layers of human articular cartilage.Biochem. J. 209, 387–400.

    CAS  PubMed  Google Scholar 

  • Bulstra, S., Drukker, J., Kuijer, R. W. B. &Van der Linden, A. (1993) Thionin staining of paraffin and plastic embedded sections of cartilage.Biotech. Histochem. 68, 20–8.

    CAS  PubMed  Google Scholar 

  • Camplejohn, K. &Allard, S. (1988) Limitations of Safranin O staining in proteoglycan-depleted cartilage demonstrated with monoclonal antibodies.Histochemistry. 89, 185–8.

    Article  CAS  PubMed  Google Scholar 

  • Chen, K. &Wight, T. (1984) Proteoglycans in arterial smooth muscle cell cultures. an ultrastructural histochemical analysis.J. Histochem. Cytochem. 32, 347–57.

    CAS  PubMed  Google Scholar 

  • Conn, H., Darrow, M. &Emmel, V. (1966)Staining Procedures of the Biological Stain Commission, Baltimore: Williams & Wilkins.

    Google Scholar 

  • Farndale, R., Sayers, C. &Barrett, A. (1982) A direct spectrophotometric microassay for sulphated glycosaminoglycans in cartilage cultures.Connect. Tissue. 9, 247–8.

    CAS  Google Scholar 

  • Grodzinsky, A. (1983) Electromechanical and physicochemical properties of connective tissue.CRC Crit. Rev. Biomed. Eng. 9, 133–99.

    CAS  Google Scholar 

  • Haigh, M. &Scott, J. (1986) A method of processing tissue sections for staining with Cupromeronic blue and other dyes, using CEC techniques for light and electron microscopy.Basic Appl. Histochem. 30, 479–86.

    CAS  PubMed  Google Scholar 

  • Horobin, R. (1982)Histochemistry. An Explanatory Outline of Histochemistry and Biophysical Staining. Stuttgart: Gustav Fischer.

    Google Scholar 

  • Hunziker, E., Ludi, A. &Herrmann, W. (1992) Preservation of cartilage matrix proteoglycans using cationic dyes chemically related to ruthenium hexamine trichloride.J. Histochem. Cytochem. 40, 909–17.

    CAS  PubMed  Google Scholar 

  • Jortikka, M., Lammi, M., Parkkinen, J. &Tammi, M. (1993) A high sensitivity dot-blot assay for proteoglycans by cuprolinic blue precipitation.Connect. Tissue.29, 1–10.

    Google Scholar 

  • Juarranz, A., Ferrer, J., Tato, A., Canete, M. &Stockert, J. (1987) Metachromatic staining and electron dense reaction of glycosaminoglycans by means of Cuprolinic Blue.Histochem. J. 19, 1–6.

    Article  CAS  PubMed  Google Scholar 

  • Kantor, T. &Schubert, M. (1957) A method for the desulfation of chondroitin sulfate.J. Am. Chem. Soc. 79, 152–3.

    Article  CAS  Google Scholar 

  • Kelly, J., Bloom, G. &Scott, J. (1963) Quaternary ammonium compounds in connective tissue histochemistry: I. Selective unblocking.J. Histochem. Cytochem. 11, 791–8.

    CAS  Google Scholar 

  • Kempson, G., Spivey, C., Swanson, S. &Freeman, M. (1971) Patterns of cartilage stiffness on normal and degenerative human femoral heads.J. Biomech. 4, 597–609.

    CAS  PubMed  Google Scholar 

  • Király, K., Lammi, M., Arokoski, J., Lapveteläinen, T., Tammi, M., Helminen, H. &Kiviranta, I. (1996) The presence of Safranin O during the specimen processing decreases the loss of glycosaminoglycans from the bovine articular cartilage.Histochem. J. 28, 99–107.

    Article  PubMed  Google Scholar 

  • Kiviranta, I., Tammi, M., Lappalainen, R., Kuusela, T. &Helminen, H. (1980). The rate of calcium extraction during EDTA decalcification from thin bone slices as assessed with atomic absorption spectrophotometry.Histochemistry.68, 119–27.

    Article  CAS  PubMed  Google Scholar 

  • Kiviranta, I., Jurvelin, J., Tammi, M., Säämänen, A.-M. &Helminen, H. (1985a) Microspectrophotometric quantitation of glycosaminoglycans in articular cartilage sections stained with Safranin O.Histochemistry 82, 249–55.

    Article  CAS  PubMed  Google Scholar 

  • Kiviranta, I., Tammi, M., Jurvelin, J. &Säämänen, A.-M. (1985b) Demonstration of chondroitin sulphate and glyco-proteins in articular cartilage matrix using Periodic Acid-Schiff (PAS) method.Histochemistry. 83, 303–6.

    Article  CAS  PubMed  Google Scholar 

  • Lammi, M. &Tammi, M. (1988) Densitometric assay of nanogram quantities of proteoglycans precipitated on nitrocellulose membrane with Safranin O.Anal Biochem. 168, 352–7.

    Article  CAS  PubMed  Google Scholar 

  • Lillie, R. (1965)Histopathologic Technic and Practical Histochemistry, 3rd edn. New York: McGraw-Hill.

    Google Scholar 

  • Lohmander, S. (1988) Proteoglycans of joint cartilage. Structure, function, turnover and role as markers of joint disease.Bailliere Clin. Rheum. 2, 37–62.

    CAS  Google Scholar 

  • Lucy, J., Dingle, J. &Fell, H. (1961) Studies on the mode of action of excess vitamin A.2. A possible role of intracellular proteases in the degradation of cartilage matrix.Biochem. J. 79, 500–8.

    CAS  PubMed  Google Scholar 

  • Maroudas, A. (1970) Distribution and diffusion of solutes in articular cartilage.Biophys. J. 10, 365–79.

    CAS  PubMed  Google Scholar 

  • Maroudas, A. &Thomas, H. (1970) A simple physicochemical micromethod for determining fixed anionic groups in connective tissue.Biochim. Biophys. Acta. 215, 214–16.

    CAS  PubMed  Google Scholar 

  • Módis, L. (1974) Topo-optical investigation of mucopolysaccharides (acid glycosaminoglycans). InHandbuch der Histochemie (edited byGraumann, W. &Neumann, K.). Stuttgart: Gustav Fischer.

    Google Scholar 

  • Módis, L. (1991).Organization of the Extracellular matrix: A Polarisation Microscopic Approach. Boca Raton: CRC Press.

    Google Scholar 

  • Muir, H. (1982) Proteoglycans as organizers of the intercellular matrix.Biochem. Soc. Trans. 11, 613–22.

    Google Scholar 

  • Poole, A. (1970) The relationship between Toluidine Blue staining and hexuronic acid content of cartilage matrix.Histochem. J. 2, 425–30.

    CAS  PubMed  Google Scholar 

  • Romhányi, G. (1963) Über die submikroskopische strukturelle Grundlage der metachromatischen Reaktion.Acta Histochem. 15, 201–33.

    PubMed  Google Scholar 

  • Rosenberg, L (1971) Chemical basis of the histological use of Safranin O in the study of articular cartilage.J. Bone Joint Surg. Am. 53A, 69–82.

    Google Scholar 

  • Scott, J. (1972) Histochemistry of Alcian Blue. III. The molecular biological basis of staining by Alcian Blue 8GX and analogous phthalocyanins.Histochemie 32, 191–212.

    Article  CAS  PubMed  Google Scholar 

  • Scott, J. (1975) Physiological function and chemical composition of pericellular proteoglycan (an evolutionary view).Philos. Trans. R. Soc. B 271, 235–42.

    Google Scholar 

  • Scott, J. &Dörling, J. (1965) Differential staining of acid glycosaminoglycans (mucopolysaccharides) by alcian blue staining in salt solutions.Histochemie 5, 221–33.

    Article  CAS  PubMed  Google Scholar 

  • Scott, J. &Dörling, J. (1969) Periodate oxidation of acid polysaccharides III. A PAS method for chondroitin sulphates and other glycosamino-glucuronans.Histochemie 19, 295–301.

    Article  CAS  PubMed  Google Scholar 

  • Shepard, N. &Mitchell, N. (1976) Simultaneous localization of proteoglycan by light and electron microscopy using toluidine blue O: a study of epiphyseal cartilage.J. Histochem. Cytochem. 24, 621–9.

    CAS  PubMed  Google Scholar 

  • Stockwell, R. &Scott, J. (1967) Distribution of acid glycosaminoglycans in human articular cartilage.Nature 215, 1376–8.

    CAS  PubMed  Google Scholar 

  • Szirmal J. (1963) Quantitative approaches in the histochemistry of mucopolysaccharides.J. Histochem. Cytochem. 11, 24–34.

    Google Scholar 

  • Szirmai, J. (1969) Structure of cartilage. InAging of Connective and Skeletal Tissue (edited byEngel, A. &Larsson, T.). pp. 163–84. Stockholm: Nordiska Bokhandeln Forlag.

    Google Scholar 

  • Taylor, K. &Jeffree, G. (1969) A new basic metachromatic dye, 1∶9-Dimethyl Methylene Blue.Histochem. J. 1, 199–204.

    Article  CAS  PubMed  Google Scholar 

  • Templeton, D. (1988) The basis and applications of the dimethylmethylene blue binding assay for sulphated glycosaminoglycans.Connect. Tissue. 17, 23–32.

    CAS  Google Scholar 

  • Terner, J. (1964) Histochemical alkylation: a study of methyliodide and its effects on tissues.J. Histochem. Cytochem. 12, 504–11.

    CAS  PubMed  Google Scholar 

  • Thyberg, J., Lohmander, S. &Friberg, U. (1973) Electron microscopic demonstration of proteoglycans in guinea pig epiphyseal cartilage.J. Ultrastruct. Res. 45, 407–27.

    Article  CAS  PubMed  Google Scholar 

  • Van Kuppevelt, T., Domen, J., Cremers, F. &Kuyper, C. (1984) Staining of proteoglycans in mouse lung alveoli. I. Ultrastructural localization on anionic sites.Histochem. J. 16, 657–69.

    PubMed  Google Scholar 

  • Venn, M. &Maroudas, A. (1977) Chemical composition and swelling of normal and osteoarthrotic femoral head cartilage.Ann. Rheum. Dis. 36, 121–9.

    CAS  PubMed  Google Scholar 

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Király, K., Lapveteläinen, T., Arokoski, J. et al. Application of selected cationic dyes for the semiquantitative estimation of glycosaminoglycans in histological sections of articular cartilage by microspectrophotometry. Histochem J 28, 577–590 (1996). https://doi.org/10.1007/BF02331378

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  • DOI: https://doi.org/10.1007/BF02331378

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