The host's genetic background determines the extent of angiogenesis induced by schistosome egg antigens

Acta Tropica

Volumn 99, Issue 2-3, 2006, Pages 243-251

  Van de Vijver, Koen K ^a,b   Colpaert, Cecile G ^a   Jacobs, Werner ^a   Kuypers, Kristel ^a   Hokke, Cornelis H ^b   Deelder, André M ^b   Van Marck, Eric A ^a  

^a ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Angiogenesis; Fibrosis; Granuloma; Inbred mice; Schistosomiasis; Soluble egg antigens

Indexed keywords

ANTIGEN; CD34 ANTIGEN; KI 67 ANTIGEN;

ANTIGEN; GENETICS; HOST-PATHOGEN INTERACTION; RODENT; SCHISTOSOMIASIS;

ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EGG; GRANULOMATOUS INFLAMMATION; IMMUNOHISTOCHEMISTRY; INBRED STRAIN; LIVER; LIVER FIBROSIS; LIVER GRANULOMA; LIVER PRESERVATION; MALE; MORTALITY; MOUSE; MOUSE STRAIN; NONHUMAN; PARASITE IDENTIFICATION; POLARIZATION; PORTAL VEIN; SCHISTOSOMA HEMATOBIUM; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS; STATISTICAL ANALYSIS; STROMA;

ANIMALS; ANTIGENS, HELMINTH; GENETIC PREDISPOSITION TO DISEASE; GRANULOMA; IMMUNOHISTOCHEMISTRY; LIVER; LIVER CIRRHOSIS; MALE; MICE; MICE, INBRED BALB C; MICE, INBRED C3H; MICE, INBRED C57BL; NEOVASCULARIZATION, PATHOLOGIC; SCHISTOSOMA HAEMATOBIUM; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS HAEMATOBIA; SCHISTOSOMIASIS MANSONI; SPECIFIC PATHOGEN-FREE ORGANISMS;

MURINAE; SCHISTOSOMA; SCHISTOSOMA MANSONI;

EID: 33750499085     PISSN: 0001706X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.actatropica.2006.08.011     Document Type: Article

References (40)

1. Baptista A.P., and Andrade Z.A. Angiogenesis and schistosomal granuloma formation. Mem. Inst. Oswaldo Cruz 100 (2005) 183-185
2. Bergman I., and Loxley R. Two improved and simplified methods for the spectrophotometric determination of hydroxyproline. Anal. Chem. 35 (1963) 1961-1965
3. Carmeliet P., and Jain R.K. Angiogenesis in cancer and other diseases. Nature 407 (2000) 249-257
4. Cheever A.W., Duvall R.H., Hallack-TA J., Minker R.G., Malley J.D., and Malley K.G. Variation of hepatic fibrosis and granuloma size among mouse strains infected with Schistosoma mansoni. Am. J. Trop. Med. Hyg. 37 (1987) 85-97
5. Cummings R.D., and Nyame A.K. Schistosome glycoconjugates. Biochim. Biophys. Acta 1455 (1999) 363-374
6. Deelder A.M., Ruitenberg E.J., Van Marck E.A., and Claas F.H. H-2 linked response to Schistosoma mansoni in the mouse: immunological and immunopathological aspects. Contrib. Microbiol. Immunol. 7 (1983) 3-8
7. Dessein A.J., Hillaire D., Elwali N.E., Marquet S., Mohamed A.Q., Mirghani A., Henri S., Abdelhameed A.A., Saeed O.K., Magzoub M.M., and Abel L. Severe hepatic fibrosis in Schistosoma mansoni infection is controlled by a major locus that is closely linked to the interferon-gamma receptor gene. Am. J. Hum. Genet. 65 (1999) 709-721
8. El Awady M.K., Gad Y.Z., Wen Y., Eassawi M., Effat L., Amr K.S., Ismail S., and Christ G.J. Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells. World J. Urol. 19 (2001) 263-266
9. El Meneza S., Olds G.R., Kresina T.F., and Mahmoud A.A. Dynamics of hepatic connective tissue matrix constituents during murine Schistosoma mansoni infection. Hepatology 9 (1989) 50-56
10. Freedman D.O., and Ottesen E.A. Eggs of Schistosoma mansoni stimulate endothelial cell proliferation in vitro. J. Infect. Dis. 158 (1988) 556-562
11. Grimaud J.A. Cell-matrix interactions in schistosomal portal fibrosis: a dynamic event. Mem. Inst. Oswaldo Cruz 82 (1987) 55-65
12. Hokke C.H., and Deelder A.M. Schistosome glycoconjugates in host-parasite interplay. Glycoconj. J. 18 (2001) 573-587
13. Hokke C.H., and Yazdanbakhsh M. Schistosome glycans and innate immunology. Parasite Immunol. 27 (2005) 257-264
14. Jackson J.R., Seed M.P., Kircher C.H., Willoughby D.A., and Winkler J.D. The codependence of angiogenesis and chronic inflammation. FASEB J. 11 (1997) 457-465
15. Jacobs W., Bogers J., Deelder A., Wery M., and Van Marck E. Adult Schistosoma mansoni worms positively modulate soluble egg antigen-induced inflammatory hepatic granuloma formation in vivo. Stereological analysis and immunophenotyping of extracellular matrix proteins, adhesion molecules, and chemokines. Am. J. Pathol. 150 (1997) 2033-2045
16. Jacobs W., Kumar Singh S., Bogers J., Van de Vijver K., Deelder A., and Van Marck E. Transforming growth factor-beta, basement membrane components and heparan sulphate proteoglycans in experimental hepatic schistosomiasis mansoni. Cell Tissue Res. 292 (1998) 101-106
17. Jacobs W., Van de Vijver K., Deelder A., and Van Marck E. Morphometrical and immunopathological dissection of the hepatic Schistosoma haematobium granuloma in the murine host. Parasite 5 (1998) 299-306
18. Kanse S.M., Liang O., Schubert U., Haas H., Preissner K.T., Doenhoff M.J., and Dennis R.D. Characterisation and partial purification of Schistosoma mansoni egg-derived pro-angiogenic factor. Mol. Biochem. Parasitol. 144 (2005) 76-85
19. Lenzi H.L., Sobral A.C., and Lenzi J.A. Participation of endothelial cells in murine schistosomiasis. Br. J. Med. Biol. Res. 21 (1988) 999-1003
20. Libby P., and Schonbeck U. Drilling for oxygen: angiogenesis involves proteolysis of the extracellular matrix. Circ. Res. 89 (2001) 195-197
21. Loeffler D.A., Lundy S.K., Singh K.P., Gerard H.C., Hudson A.P., and Boros D.L. Soluble egg antigens from Schistosoma mansoni induce angiogenesis-related processes by up-regulating vascular endothelial growth factor in human endothelial cells. J. Infect. Dis. 185 (2002) 1650-1656
22. Mor F., Quintana F.J., and ohen I.R. Angiogenesis-inflammation cross-talk: vascular endothelial growth factor is secreted by activated T cells and induces Th1 polarization. J. Immunol. 172 (2004) 4618-4623
23. Pearce E.J., and MacDonald A.S. The immunobiology of schistosomiasis. Nat. Rev. Immunol. 2 (2002) 499-511
24. Pusztaszeri M., Seelentag W., and Bosman F.T. Immunohistochemical expression of endothelial markers CD31, CD34, von Willebrand Factor, and Fli-1 in normal human tissues. J. Histochem. Cytochem. 54 (2005) 385-395
25. Rodrigues V., Piper K., Couissinier P.P., Bacelar O., Dessein H., and Dessein A.J. Genetic control of schistosome infections by the SM1 locus of the 5q31-q33 region is linked to differentiation of type 2 helper T lymphocytes. Infect. Immun. 67 (1999) 4689-4692
26. Rutitzky L.I., Hernandez H.J., Yim Y.S., Ricklan D.E., Finger E., Mohan C., Peter I., Wakeland E.K., and Stadecker M.J. Enhanced egg-induced immunopathology correlates with high IFN-gamma in murine schistosomiasis: identification of two epistatic genetic intervals. J. Immunol. 174 (2005) 435-440
27. Silva L.M., Ribeiro-dos-Santos R., Soares M.B., and Andrade Z.A. Characterization of the vascular changes in schistosomal portal (pipestem) fibrosis of mice. Acta Trop. 98 (2006) 34-42
28. Silvestre J.S., Mallat Z., Tamarat R., Duriez M., Tedgui A., and Levy B.I. Regulation of matrix metalloproteinase activity in ischemic tissue by interleukin-10: role in ischemia-induced angiogenesis. Circ. Res. 89 (2001) 259-264
29. Smithers S.R., and Terry R.J. The immunology of schistosomiasis. Adv. Parasitol. 14 (1976) 399-422
30. Stadecker M.J. The development of granulomas in schistosomiasis: genetic backgrounds, regulatory pathways, and specific egg antigen responses that influence the magnitude of disease. Microbes. Infect. 1 (1999) 505-510
31. Stadecker M.J., Asahi H., Finger E., Hernandez H.J., Rutitzky L.I., and Sun J. The immunobiology of Th1 polarization in high-pathology schistosomiasis. Immunol. Rev. 201 (2004) 168-179
32. Stavitsky A.B. Regulation of granulomatous inflammation in experimental models of schistosomiasis. Infect. Immun. 72 (2004) 1-12
33. Szekanecz Z., and Koch A.E. Endothelial cells in inflammation and angiogenesis. Curr. Drug Targets Inflamm. Allergy 4 (2005) 319-323
34. Theuerkauf I., Zhou H., and Fischer H.P. Immunohistochemical patterns of human liver sinusoids under different conditions of pathologic perfusion. Virchows Arch. 438 (2001) 498-504
35. Van de Vijver K.K., Deelder A.M., Jacobs W., Van Marck E.A., and Hokke C.H. LacdiNAc- and LacNAc-containing glycans induce granulomas in an in vivo model for schistosome egg-induced hepatic granuloma formation. Glycobiology 16 (2006) 237-243
36. Van de Vijver K.K., Hokke C.H., van Remoortere A., Jacobs W., Deelder A.M., and Van Marck E.A. Glycans of Schistosoma mansoni and keyhole limpet haemocyanin induce hepatic granulomas in vivo. Int. J. Parasitol. 34 (2004) 951-961
37. Van Marck E.A., Stocker S., Grimaud J.A., Kestens L., Gigase P.L., and Deelder A.M. The implantation of sepharose beads in mouse livers as an aid in the study of hepatic schistosomal fibrosis. Experientia 36 (1980) 1116-1118
38. Vermeulen P.B., Gasparini G., Fox S.B., Colpaert C., Marson L.P., Gion M., Beliën J.A.M., de Waal R.M.W., Van Marck E., Magnani E., Weidner N., Harris A.L., and Dirix L.Y. Second international consensus on the methodology and criteria of evaluation of angiogenesis quantification in solid tumours. Eur. J. Cancer 38 (2002) 1564-1579
39. Weiss J.B., Aronstein W.S., and Strand M. Schistosoma mansoni: stimulation of artificial granuloma formation in vivo by carbohydrate determinants. Exp. Parasitol. 64 (1987) 228-236
40. Wyler D.J., Prakash S., and Libby P. Mesenchymal target cell specificity of egg granuloma-derived fibroblast growth factor in schistosomiasis. J. Infect. Dis. 155 (1987) 728-736