Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-26T21:55:54.795Z Has data issue: false hasContentIssue false

Effect of acute phase proteins, especially α2-macroglobulin, on granuloma formation around Schistosoma mansoni eggs in the rat

Published online by Cambridge University Press:  06 April 2009

J. Van Gool
Affiliation:
Laboratory of Experimental Medicine, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands
D. Van Tiel
Affiliation:
Laboratory of Experimental Medicine, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands
M. J. Doenhoff
Affiliation:
London School of Hygiene and Tropical Medicine, Winches Farm Field Station, 395 Hatfield Road, St Albans, Herts AL4 0XQ, UK
H. Van Vugt
Affiliation:
Laboratory of Experimental Medicine, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

Summary

A new model for the study of granuloma formation in the liver is described. Rats received an injection of 20 000 Schistosoma mansoni eggs in the portal vein and granuloma formation was evaluated at 3, 5 and 7 weeks post-injection. Liver collagen was estimated at the same time and serum procollagen III peptide, a marker of collagenesis, weekly. With this model, wherein the number of S. mansoni eggs and the time of injury are standardized, the effect of high levels of acute phase proteins especially α2-macroglobulin on granuloma formation was studied. It appeared that in rats with high levels of α2-macroglobulin the mean size of granulomas was significantly greater at 3 and 5 weeks compared with controls. In both groups an increase in liver collagen was observed during this period, reaching a peak at 5 weeks in the acute phase group. This model facilitates the study of the effects of S. mansoni eggs on granuloma formation.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1991

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ciba-Geigy, (1980). Wissenschaftliche Tabellen. 8e Auflage. Basel, Switzerland.Google Scholar
Davis, B. H. & Madri, J. A. (1987). Type I and type III procollagen peptides during hepatic fibrogenesis. American Journal of Pathology 126, 137–47.Google ScholarPubMed
Doenhoff, M.J., Pearson, S., Dunne, D.W., Bickle, Q., Lucas, S., Bain, J., Musallam, R. & Hassounah, O. (1981). Immunological control of hepatotoxicity and parasite egg excretion in Schistosoma mansoni infections: stage specificity of the reactivity of immune serum in T-cell deprived mice. Transactions of the Royal Society of Tropical Medicine and Hygiene 75, 4153.CrossRefGoogle ScholarPubMed
Elliott, D. E., Righthand, V. F. & Boros, D. L. (1987). Characterization of regulatory (interferon α/β) and accessory (LAF/Il 1) monokine activities from liver granuloma macrophages of Schistosoma mansoni- infected mice. Journal of Immunology 138, 2653–62.CrossRefGoogle ScholarPubMed
Gool, J. VAN, Boers, W. & Nie, I. DE (1978). Inhibitory effects of rat α2 macrofetoprotein (αM FP), an acute phase globulin, on galactosamine hepatitis. Experimental and Molecular Pathology 29, 228–40.CrossRefGoogle Scholar
Gool, J. VAN, Boers, W., Sala, M. & Ladiges, N. C. J. J. (1984). Glucocorticoids and catecholamines as mediators of acute-phase proteins, especially rat α-macro foetoprotein. Biochemical Journal 220, 125–32.CrossRefGoogle Scholar
Gool, J. VAN, Nie, I. DE, Smit, J. & Zuyderhoudt, F. M. J. (1986 b). Mechanisms by which acute phase proteins enhance development of liver fibrosis: effects on collagenase and prolyl-4-hydroxylase activity in rat liver. Experimental and Molecular Pathology 45, 160–70.CrossRefGoogle ScholarPubMed
Gool, J. VAN, Nie, I. DE, Vugt, H. VAN & Brugman, A. M. (1988). Relation between acute phase proteins and enhanced bleomycin-induced pulmonary fibrosis in the rat. Experimental and Molecular Pathology 49, 410–20.CrossRefGoogle ScholarPubMed
Gool, J. VAN, Vugt, H. VAN, Helle, M. & Aarden, L. A. (1990). The relation between stress, adrenalin, interleukin 6 and acute phase proteins in the rat. Clinical Immunology and Immunopathology (in the Press).Google ScholarPubMed
Gool, J. VAN, Vugt, H. VAN & Nie, I. DE (1986 a). Acute phase reactants enhance CCI4 induced liver cirrhosis in the rat. Experimental and Molecular Pathology 44, 157–68.CrossRefGoogle Scholar
Kivirikko, K. I., Laitinen, O. & Prockop, D. J. (1967). Modification of a specific assay for hydroxyproline in the urine. Analytical Biochemistry 19, 249–55.CrossRefGoogle Scholar
Lichtenberg, F. VON (1962). Host response to eggs of S. mansoni. I. Granuloma formation in the unsensitized laboratory mouse. American Journal of Pathology 41, 711–23.Google Scholar
Li HsÜ, S. Y., HsÜ, H. F., Davis, J. R. & Lust, G. L. (1972). Comparative studies on the lesions caused by eggs of Schistosoma japonicum and Schistosoma mansoni in livers of albino mice and rhesus monkeys. Annals of Tropical Medicine and Parasitology 66, 8997.CrossRefGoogle Scholar
Lopez De LÉon, A. & Rojkind, M. (1985). A simple micromethod for collagen and total protein determination in formalin-fixed paraffin-embedded sections. Journal of Histochemistry and Cytochemistry 33, 737–43.CrossRefGoogle ScholarPubMed
Luna, L. G. (1968). Manual of Histological Staining Methods of the Armed Forces Institute of Pathology. 3rd Edn, pp. 75–7. New York: McGraw-Hill Inc.Google Scholar
McKerrow, J. H. & Doenhoff, M.J. (1988). Schistosome proteases. Parasitology Today 4, 334–40.CrossRefGoogle ScholarPubMed
Meneza, G. E., Olds, G. R., Kresina, T. F. & Mahmoud, A. A. A. (1989). Dynamics of hepatic connective tissue matrix constituents during murine Schistosoma mansoni infection. Hepatology 9, 50–6.CrossRefGoogle ScholarPubMed
Pepys, M. P., Baltz, M. L., Musallam, R. & Doenhoff, M. J. (1980). Serum protein concentrations during Schistosoma mansoni infection in intact and T-cell deprived mice. Immunology 39, 249–54.Google ScholarPubMed
Schiller, E. & Haese, W. H. (1973). Histologic processes of healing in hepatic injury due to eggs of Schistosoma mansoni in mice following curative chemotherapy. American Journal of Tropical Medicine and Hygiene 222, 211–14.CrossRefGoogle Scholar
Schuppan, D., Dumond, J. M., Kim, K. Y., Hennings, G. & Hahn, E. G. (1986). Serum concentration of the aminoterminal procollagen type III peptide in the rat reflects early formation of connective tissue in experimental liver cirrhosis. Journal of Hepatology 3, 2737.CrossRefGoogle ScholarPubMed
Smith, B. D., McKenney, K. H. & Lustenberg, T. J. (1977). Characterization of collagen precursors found in rat/skin and rat/bone. Biochemistry 16, 2980–5.CrossRefGoogle ScholarPubMed
Smithers, S. R. & Doenhoff, M. J. (1982). Schistosomiasis. In Immunology of Parasitic Infections, 2nd Edn (ed. Cohen, S. & Warren, K. S.), pp. 527607. Oxford, London, Edinburgh and Melbourne: Blackwell Scientific Publications.Google Scholar
Takahashi, S., Dunn, M. A. & Seifter, S. (1980). Liver collagenase in murine schistosomiasis. Gastroenterology 78, 1425–31.CrossRefGoogle ScholarPubMed
Truden, J. L. & Boros, D. L. (1988). Detection of α2 macroglobulin, α1 protease inhibitor and neutral protease–antiprotease complexes within liver granulomas of schistosoma infected mice. American Journal of Pathology 130, 281–8.Google Scholar
Wiestner, M., Krieg, T., Horlein, D., Glanville, R. W., Fietzek, P. & Muller, P. K. (1979). Inhibiting effect of procollagen peptides on collagen biosynthesis in fibroblast cultures. Journal of Biological Chemistry 254, 7016–23.Google Scholar