Skip to main content
Log in

Niemann-Pick disease: Lipid storage in bone marrow macrophages

  • Papers
  • Published:
The Histochemical Journal Aims and scope Submit manuscript

Summary

A histochemical study of lipids in bone marrow smears was performed in a series of 15 cases of Niemann-Pick disease (NPD). It revealed significant differences in the amount of lipids stored in macrophages of sphingomyelinase (SMase) deficiency (types A,B) and type C. Early deposition of uniform, anisotropic droplets of sphingomyelin (Maltese-cross birefringence) in lysosomes was a feature of a 9-member group of SMase deficiency (types A,B). The type C group (six cases) was characterized by a remarkable difference in the degree of phospholipid, mainly sphingomyelin, deposition. The total amount of phospholipids was small on average, and very often inversely proportional to pronounced structural storage changes. This indirect relationship was most prominent in the early phase of the disease and grew less prominent as the disease progressed further. The stored lipid was primarily isotropic. In longer lasting cases of both categories (SMase deficiency and type C) a considerable part of the storage cell population displayed ceroid deposition giving the appearance of a ‘sea-blue histiocyte’ independent of the type of NPD, but with definite predominance in SMase deficiency. The diagnostic value of the findings is discussed, and some pathogenetic conclusions suggested, particularly as regards type C.

Lipid histochemistry of bone marrow smears is highly recommended as it represents a simple but highly efficient approach, capable of yielding valuable diagnostic information.

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.

Similar content being viewed by others

References

  • Adams, C. W. M. (1965)Neurohistochemistry, pp. 6–66. Amsterdam: Elsevier.

    Google Scholar 

  • Besley, G. T. N. (1977) Sphingomyelinase defect in Niemann-Pick disease, type C, fibroblasts.FEBS Lett. 80, 71–4.

    Google Scholar 

  • Brady, R. O. &King, F. M. (1973) Niemann-Pick's Disease. InLysosomes and Storage Diseases (edited byHers, H. G. andVan Hoof, F.) pp. 439–52. New York: Academic Press.

    Google Scholar 

  • Callahan, J. W., Khalil, M. &Gerrie, J. (1974) Isoenzymes of sphingomyelinase and the genetic defect in Niemann-Pick disease.Biochem. Biophys. Res. Commun. 58, 384–90.

    Google Scholar 

  • Christomanou, H. (1980) Niemann-Pick disease, type C: evidence for the deficiency of an activating factor stimulating sphingomyelin and glucocerebroside degradation.Hoppe-Seyler's Z. Physiol. Chem. 361, 1489–502.

    Google Scholar 

  • Crocker, A. C. &Farber, S. (1958). Niemann-Pick's disease: a review of eighteen patients.Medicine, Baltimore 37, 1–96.

    Google Scholar 

  • Elleder, M. (1977) Lipidhistochemistry—a critical survey.Acta histochemical, Jena Suppl. 9, 239–65.

    Google Scholar 

  • Elleder, M. (1981) Chemical characterization of age pigments. InAge Pigments (edited bySohal, R. S.), pp. 204–41. Elsevier, North-Holland: Biomedical Press.

  • Elleder, M. (1982) Histochemistry of lipids. Methodological study and evaluation of its significance in diagnosis of lipid storage diseases. PhD thesis (in Czechoslovakian).

  • Elleder, M. &Lojda, Z. (1971) Studies in lipid histochemistry. VI. Problems of extraction with acetone in lipid histochemistry.Histochemie 28, 68–87.

    Google Scholar 

  • Elleder, M. &Lojda, Z. (1973a) Studies in lipid histochemistry. XI. New, rapid, simple and selective method for the demonstration of phospolipids.Histochemie 36, 149–66.

    Google Scholar 

  • Elleder, M. &Lojda, Z. (1973b) Studies in lipid histochemistry. XII. Histochemical detection of sphingomyelin.Histochemie 37, 371–3.

    Google Scholar 

  • Elleder, M. &Jirásek, A. (1981) Neuropathology of various types of Niemann-Pick disease.Acta neurpathol., Berl. Suppl. VII, 134–5.

    Google Scholar 

  • Elleder, M., Šmíd, F., Harzer, K. &Čihula, J. (1980) Niemann-Pick disease. Analysis of liver tissue in sphingomyelinase-deficient patients.Virchows Arch. Path. Anat. and Histol. 385, 215–31.

    Google Scholar 

  • Farquahar, J. W. &Claireaux, A. E. (1952) Familiar hemophagocytic reticulosis.Arch. Dis. Child. 27, 519–25.

    Google Scholar 

  • Ferrans, V. J., Roberts, W. C., Levy, R. I. &Fredrickson, D. S. (1973) Chylomikrons and the formation of foam cells in type I hyperlipoproteinemia.Am. J. Path. 70, 253–72.

    Google Scholar 

  • Fredrickson, D. S. & Sloan, H. R. (1972) Sphingomyelin lipidosis: Niemann-Pick disease. InThe Metabolic Basis of Inherited Disease (edited byStanbury, J. B. Wyngaarden, J. B. andFredrickson, D. S.), pp. 783–807.

  • Frost, P., Tanaka, Y. &Spaeth, G. L. (1966) Fabry's disease—glycolipid lipidosis. Histochemical and electronmicroscopic studies of two cases.Am. J. Med. 40, 618–27.

    Google Scholar 

  • Grover, W. D. &Naiman, J. L. (1971) Progressive paralysis of vertical gaze in lipid storage disease.Neurology, Mineapolis 21, 896–9.

    Google Scholar 

  • Harzer, K., Anzil, A. P. &Schuster, I. (1977) Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction dependent: evidence for a component defect in Niemann-Pack disease type C is spurious.J. Neurochem. 29, 1155–7.

    Google Scholar 

  • Harzer, K. &Benz, H. U. (1976) Sphingomyelinoses (Niemann-Picksche Erkrankung). InHandbuch der inneren Medizin, Band VII/4 Fettstoffwechsel (edited bySchettler, G., Greten H., Schlierf, G., Seidel, D.), pp. 525–46. Berlin, Heidelberg: Springer Verlag.

    Google Scholar 

  • Harzer, K., Ruprecht, K. W., Seuffer-Schulze, D., &Jans, U. (1978) Morbus Niemann-Pick B—enzymatisch gesichert-mit unerwarteter retinaler Beteiligung.Albrecht von Graefes Arch. Klin. Ophthalmol. 206, 79–88.

    Google Scholar 

  • Jonas, O. (1966) Ceroid storage in a child with a Niemann-Pick type syndrome.Med. J. Australia 2, 551–4.

    Google Scholar 

  • Kattlove, H. E., Williams, J. C., Gaynor, E., Spivack, M., Bradley, R. M. &Brady, R. O. (1969) Gaucher cells in chronic myelocytic leukemia: an acquired abnormality.Blood 33, 379–90.

    Google Scholar 

  • Knight, J. A. &Myers, G. G. (1973) Type IV hyperlipidemia in the GM1 gangliosidosis.Am. J. clin. Path. 59, 124.

    Google Scholar 

  • Lake, B. D. (1981) Metabolic disoorders: general considerations. InPediatric Pathology (edited byBerry, C. L.), pp. 617–39. Berlin, Heidelberg, New York: Springer Verlag.

    Google Scholar 

  • Landing, B. H., Straus, L., Crocker, A. C., Braunstein, H., Henley, W. L., Will, J. R. &Sauders, M. (1961) Thrombocytopenic purpura with histiocytosis of the spleen.New England J. Med. 265, 572–7.

    Google Scholar 

  • Lennert, K., Nierdorf, H. R. &Blümcke, S. (1972) Lymphadenitis with massive hemophagocytic sinus histiocytosis.Virchows Arch. Abt. B Zellpath. 10, 14–29.

    Google Scholar 

  • Lojda, Z., Gossrau, R. &Schiebler, T. H. (1979)Enzyme histochemistry. A laboratory manual. Berlin, Heidelberg, New York: Springer Verlag.

    Google Scholar 

  • MacMahon, H. E., Bedizel, M. &Ellis, C. A. (1963) Familial hemofagocytic lymphohistiocytosis.Pediatrics 32, 868–79.

    Google Scholar 

  • Neville, B. G. R., Lake, B. D., Stephens, R. &Sanders, M. D. (1973) A neurovisceral storage disease with vertical supranuclear ophthalmoplegia and its relationship to Niemann-Pick disease—a report of nine cases.Brain 96, 97–120.

    Google Scholar 

  • Norman, R. M., Forrester, R. M. &Tingey, A. H. (1967) The juvenile form of Niemann-Pick disease.Arch. Dis. Childh. 42, 91–6.

    Google Scholar 

  • Parker, A. C., Bain, A. D., Brydon, W. G., Harkness, R. A., Smith, I. I. &Boyd, D. H. A. (1978) Sea-blue histiocytosis associated with hyperlipidaemia.J. clin Path. 29, 634–8.

    Google Scholar 

  • Patrick, A. D. &Lake, B. D. (1973) Wolman's disease. InLysosomes and Storage Diseases (edited byHers, H. G. andVan Hoof, F.), pp. 453–73. London, New York: Academic Press.

    Google Scholar 

  • Pellissier, J. F., Hassoun, J., Gambarelli, P. A., Bryon, P. A., Casanova, P. &Toga, M. (1976) Maladie de Niemann-Pick type “C” de Crocker. Etude ultrastructurele dún cas.Acta neuropathol, Berl. 34, 65–76.

    Google Scholar 

  • Philippart, M., Martin, L., Martin, J. J. &Menkes, J. H. (1969) Niemann-Pick disease. Morphological and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C).Arch. Neurol. 20, 227–38.

    Google Scholar 

  • Reidbord, H. R., Horvat, B. L. &Fisher, E. R. (1972) Splenic lipidosis. Histochemical and ultrastructural differentiation with special reference to the syndrome of the sea-blue.Arch. Path. 93, 518–24.

    Google Scholar 

  • Roberts, W. C., Levy, R. I. &Fredrickson, D. S. (1970) Hyperlipoproteinemia. A review of the five types with first report on necropsy findings in type 3.Arch. Pathol. 90, 46–56.

    Google Scholar 

  • Rosai, J. &Dorfman, R. F. (1972) Sinus histiocytosis with massive lymphadenopathy — a pseudolymphomatous benign disorder. Analysis of 34 cases.Cancer 30, 1174–978.

    Google Scholar 

  • Tanaka, Y., Frost, P. &Spaeth, G. L. (1965) Figures myeliniques dans les cellules spumeuses de la maladie de Fabry.Nouv. Rev. Franc. d'hemat. 5, 425–39.

    Google Scholar 

  • Vanier, M.-TH., Revol, A. &Fichet, M. (1980) Sphingomyelinase activities of various human tissues in control subjects and in Niemann-Pick disease—development and evaluation of a microprocedure.Clinica chimica Acta 106, 257–67.

    Google Scholar 

  • Winsor, E. J. T. &Welch, J. P. (1978) Genetic and demographic aspects of Nova Scotia Niemann-Pick disease (type D).Am. J. Hum. Genet 30, 530–8.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Elleder, M., Hrodek, J. & Čihula, J. Niemann-Pick disease: Lipid storage in bone marrow macrophages. Histochem J 15, 1065–1077 (1983). https://doi.org/10.1007/BF01003970

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01003970

Keywords

Navigation