Gangliosides of the stroma layer participate in the interferon-gamma receptor-dependent controls of myelopoiesis

Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids

Volumn 1761, Issue 9, 2006, Pages 1030-1040

  Andrade, Claudia M B ^a   Ziulkoski, Ana L ^a,c   dos Santos, Aline X S ^a   Boldrini, Leonardo C ^b   Trindade, Vera M T ^a   Borojevic, Radovan ^b   Guma, Fátima C R ^a  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^b FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^c Feevale University   (Brazil)

Author keywords

Ganglioside; GM CSF; Haemopoiesis; Myelopoiesis

Indexed keywords

GAMMA INTERFERON RECEPTOR; GANGLIOSIDE; GANGLIOSIDE GM3; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; MONOCLONAL ANTIBODY; SCATTER FACTOR; SPHINGOLIPID;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BIOAVAILABILITY; CELL CULTURE; CELL INTERACTION; CELL LINE; CELL PROLIFERATION; CELL STIMULATION; CELL SURVIVAL; KNOCKOUT MOUSE; LIVER CELL CULTURE; MICROENVIRONMENT; MOUSE; MYELOPOIESIS; NONHUMAN; PRIORITY JOURNAL; QUALITATIVE ANALYSIS; QUANTITATIVE STUDY; STROMA; STROMA CELL; SUPERNATANT; WILD TYPE;

ANIMALS; CELL LINE; CELL PROLIFERATION; CELL SURVIVAL; COCULTURE TECHNIQUES; G(M3) GANGLIOSIDE; GANGLIOSIDES; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; LIVER; MICE; MICE, KNOCKOUT; MYELOPOIESIS; RECEPTORS, INTERFERON; SIGNAL TRANSDUCTION; SPHINGOLIPIDS; STROMAL CELLS;

EID: 33748442165     PISSN: 13881981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbalip.2006.07.009     Document Type: Article

References (43)

1. Hamilton J.A. GM-CSF in inflammation and autoimmunity. Trends Immunol. 23 (2002) 403-408
2. Holgate S.T. Epithelial damage and response. Clin. Exp. Allergy 30 S1 (2000) 37-41
3. Mann A., Breuhahn K., Schirmacher P., and Blessing M. Keratinocyte-derived granulocyte-macrophage colony stimulating factor accelerates wound healing: stimulation of keratinocyte proliferation, granulation tissue formation, and vascularization. J. Invest. Dermatol. 117 (2001) 1382-1390
4. Franzen R., Bouhy D., and Schoenen J. Nervous system injury: focus on the inflammatory cytokine "granulocyte-macrophage colony stimulating factor". Nuerosci. Lett. 361 (2004) 76-78
5. Desmoulière A., Tuchweber B., and Gabbiani G. Role of myofibroblast differentiation during liver fibrosis. J. Hepatol. 22 S2 (1995) 61-64
6. Bretscher V., Andreutti D., Neuville P., Martin M., Martin F., Lefebvre O., Gilles C., Benzonana G., and Gabbiani G. GM-CSF expression by tumor cells correlates with aggressivity and with stroma reaction formation. J. Submicrosc. Cytol. Pathol. 32 (2000) 525-533
7. Alvarez-Silva M., Silva L.C., and Borojevic R. Cell membrane-associated proteoglycans mediate extramedullar myeloid proliferation in granulomatous inflammatory reactions to schistosome eggs. J. Cell Sci. 104 (1993) 477-484
8. Alvarez-Silva M., Pinazo A.C., El-Cheikh M.C., and Borojevic R. Myelopoietic competence of stroma composed of hepatic granuloma-derived connective tissue cells or skin fibroblasts. Braz. J. Med. Biol. Res. 27 (1994) 2143-2152
9. Alvarez-Silva M., and Borojevic R. GM-CSF and IL-3 activities in schistosomal liver granulomas are controlled by stroma-associated heparan-sulfate proteoglycans. J. Leukocyte Biol. 59 (1996) 435-441
10. Modrowski D., Basle M., Lomri A., and Marie P.J. Syndecan-2 is involved in the mitogenic activity, signaling of granulocyte-macrophage colony-stimulating factor in osteoblasts. J. Biol. Chem. 275 (2000) 9178-9185
11. Wettreich A., Sebollela A., Carvalho M.A., Azevedo S.P., Borojevic R., Ferreira S.T., and Coelho-Sampaio T. Acidic pH modulates the interaction between human granulocyte-macrophage colony-stimulating factor and glycosaminoglycans. J. Biol. Chem. 274 (1999) 31468-31475
12. Carvalho M.A., Arcanjo K., Silva L.C.F., and Borojevic R. The capacity of connective tissue stromas to sustain myelopoiesis depends both upon the growth factors and the local intercellular environment. Biol. Cell 92 (2000) 605-614
13. Borojevic R., Carvalho M.A., Corrêa-Junior J.D., Arcanjo K., Gomes L., Joazeiro P.P., Balduino A., Wettreich A., and Coelho-Sampaio T. Stroma-mediated granulocye-macrophage colony-stimulating factor (GM-CSF) control of myelopoiesis: spatial organisation of intercellular interactions. Cell Tissue Res. 313 (2003) 55-62
14. Kaucic K., Grovas A., Li R., Quinones R., and Ladisch S. Modulation of human myelopoiesis by human gangliosides. Exp. Hematol. 22 (1994) 52-59
15. Bharti A.C., and Singh S.M. Induction of apoptosis in bone marrow cells by gangliosides produced by a T cell lymphoma. Immunol. Lett. 72 (2000) 39-48
16. Bharti A.C., and Singh S.M. Gangliosides derived from a T cell lymphoma inhibit bone marrow cell proliferation and differentiation. Int. Immunopharmacol. 1 (2001) 155-165
17. Sietsma H., Nijhol W., Dontje B., Vellenga E., Kamps W.A., and Kok J.W. Inhibition of hemopoiesis in vitro by neuroblastoma-derived gangliosides. Cancer Res. 58 (1998) 4840-4844
18. Nakamura M., Kirito K., Yamanoi J., Wainai T., Nojiri H., and Saito M. Ganglioside GM3 can induce megakaryocytoid differentiation of human leukemia cell line K562 cells. Cancer Res. 51 (1991) 1940-1945
19. Ziulkoski A.L., Andrade C.M.B., Crespo P.M., Sisti E., Trindade V.M.T., Daniotti J.L., Guma F.C.R., and Borojevic R. Gangliosides of myelosupportive stroma cells are transferred to myeloid progenitors and are required for their survival and proliferation. Biochem. J. 394 (2006) 1-9
20. Boloukhère M., Baldo-Correa E., and Borojevic R. Experimental schistosomiasis mansoni: characterization of connective tissue cells in hepatic periovular granulomas. J. Submicrosc. Cytol. Pathol. 25 (1993) 505-517
21. Dutra H.S., Rossi M.I.D., Azevedo S.P., El-Cheikh M.C., and Borojevic R. Haematopoietic capacity of colony-forming cells mobilised in hepatic inflammatory reactions as compared to that of normal bone marrow cells. Res. Immunol. 148 (1997) 437-444
22. Rossi M.I.D., Dutra H.S., El-Cheikh M.C., Bonomo A., and Borojevic R. Extramedullar B-lymphopoiesis in liver schistosomal granulomas: presence of the early stages and inhibition of the full B cell differentiation. Int. Immunol. 11 (1999) 509-518
23. Oliveira V.R., El-Cheikh M.C., Aguiar A.M., Balduino A., Pinho M.F.B., Reis L.F.L., and Borojevic R. Schistosoma mansoni egg-induced hepatic granulomas in mice deficient for the interferon-gamma receptor have altered populations of macrophages, lymphocytes and connective tissue cells. Microbes Infect. 2 (2000) 1817-1826
24. Jang J.H., and Surh Y.J. Protective effect of resveratrol on beta-amyloid-induced oxidative PC12 cell death. Free Radical Biol. Med. 34 8 (2003) 1100-1110
25. Svennerholm L. Quantitative estimation of sialic acids a colorimetric resorcinol-hydrochloric acid method. Biochim. Biophys. Acta 24 (1957) 604-611
26. Li R., Manela J., Kong Y., and Ladisch S. Cellular gangliosides promote growth factor-induced proliferation of fibroblasts. J. Biol. Chem. 275 44 (2000) 34213-34223
27. Peterson G.L. Review of the Folin phenol protein quantitation method of Lowry. Anal. Biochem. 100 (1979) 201-220
28. Giraudo C.G., Rosales-Fritz V.M., and Maccioni H.J. GA2/GM2/GD2 synthase localizes to the trans-Golgi network of CHO-K1 cells. Biochem. J. 342 (1999) 633-640
29. Crespo P.M., Zurita A.R., and Daniotti J.L. Effect of gangliosides on the distribution of a glycosylphosphatidylinositol-anchored protein in plasma membrane from Chinese Hamster Ovary-K1 cells. J. Biol. Chem. 277 (2002) 44731-44739
30. Hakomori S. Bifunctional role of glycosphingolipids. J. Biol. Chem. 265 (1990) 18713-18718
31. Hakomori S., and Handa K. Glycosphingolipid-dependent cross-talk between glycosynapses interfacting tumor cells with their host cells: essential basis to define tumor malignancy. FEBS Lett. 531 (2002) 88-92
32. Liu Y., Li R., and Ladisch S. Exogenous gangliosides GD1a enhances epidermal growth factor receptor binding and dimerization. J. Biol. Chem. 279 35 (2004) 36481-36489
33. Miljan E.A., and Bremer E.G. Regulation of growth factor receptors by gangliosides. Sci. STKE 160 (2002) RE15
34. Toledo M.S., Suzuki E., Handa K., and Hakomori S. Effect of gangliosides and tetraspanins in microdomaisns on interaction of integrin with fibroblast growth factor receptor. J. Biol. Chem. 280 16 (2005) 16227-16234
35. Olshefski R., and Ladish S. Intracellular transfer of shed tumor cell gangliosides. FEBS Lett. 386 (1996) 11-14
36. Sorice M., Parolini I., Sansolini T., Garofalo T., Dolo V., Sargiacomo M., Tai T., Peschle C., Torrisi M.R., and Pavan A. Evidence for the existence of ganglioside-enriched plasma membrane domains in human peripheral lymphocytes. J. Lipid Res. 38 (1997) 969-980
37. Yu J.M., Emmons R.V.B., Hanazono Y., Sellers S., Young N.S., and Dunbar C.E. Expression of interferon-γ by stromal cells inhibits murine long-term repopulating hematopoietic stem cell activity. Exp. Hematol. 27 (1999) 895-903
38. Kato K., Kamezaki K., Shimoda K., Numata A., Haro T., Aoki K., Ishikawa F., Takase K., Ariyama H., Matsuda T., Miyamoto T., Nagafuji K., Gondo H., Nakayama K., and Harada M. Intercellular signal transduction of interferon on the suppression of haematopoietic cell growth. Br. J. Haematol. 123 (2003) 528-535
39. Pitha P.M., Vengris V.E., and Reynolds Jr. F.H. The role of cell membrane in the antiviral effect of interferon. J. Supramol. Struct. 4 (1976) 467-473
40. Chany C., Rousset S., and Chany-Fournier F. Role of membrane receptors in the biological effect of interferon. Tex. Rep. Biol. Med. 82 (1981) 307-312
41. Ding Y., Ma K., and Tsui Z.C. Induction of nitric oxide production by ganglioside GM3 in murine peritoneal macrophages activated for tumor cytotoxicity. In Vivo 12 (1998) 357-361
42. Hirano T., Hizuta A., Tanaka N., and Orita K. Enhancement of experimental metastasis by gamma-interferon in a murine adenocarcinoma. Acta Med. Okayama 50 (1996) 11-16
43. Bacso Z., Bene L., Damjanovich L., and Damjanovich S. INF-gamma rearranges membrane topography of MHC-1 and ICAM-1 in colon carcinoma cells. Biochem. Biophys, Res. Commun. 290 (2002) 635-640