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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1979 Jul;76(7):3367–3371. doi: 10.1073/pnas.76.7.3367

Ganglioside inhibition of fibronectin-mediated cell adhesion to collagen.

H K Kleinman, G R Martin, P H Fishman
PMCID: PMC383826  PMID: 291010

Abstract

Fibronectin mediates the adhesion of cells to collagen by first binding to the collagen substrate, followed by attachment of the cells to the fibronectin-collagen complex. Bovine brain gangliosides were found to block fibronectin-mediated cell adhesion to collagen in a concentration-dependent manner. The gangliosides did not block the binding of fibronectin to collagen but did prevent the attachment of the cells to the fibronectin-collagen complex. Of the individual gangliosides tested, GT1 and GD1a were the most effective inhibitors followed by GD1b greater than GM1 greater than GM2; GM3 was not an inhibitor. The inhibition of cell adhesion also was observed with the oligosaccharide portion of the gangliosides, but not with ceramides or with a variety of free sugars or glycosaminoglycans. Mild periodate oxidation of mixed gangliosides or of GD1a modified their sialic acid residues and the oxidized gangliosides were no longer inhibitory; subsequent reduction with NaBH4 did not restore the inhibitory activity of the modified gangliosides. These results suggest that specific gangliosides or related sialic acid-containing glycoconjugates on the cell surface may act as the receptors for fibronectin.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AMINOFF D. Methods for the quantitative estimation of N-acetylneuraminic acid and their application to hydrolysates of sialomucoids. Biochem J. 1961 Nov;81:384–392. doi: 10.1042/bj0810384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brady R. O., Fishman P. H. Biosynthesis of glycolipids in virus-transformed cells. Biochim Biophys Acta. 1974 Sep 9;355(2):121–148. doi: 10.1016/0304-419x(74)90001-8. [DOI] [PubMed] [Google Scholar]
  3. Chen L. B., Moser F. G., Chen A. B., Mosesson M. W. Distribution of cell surface LETS protein in co-cultures of normal and transformed cells. Exp Cell Res. 1977 Sep;108(2):375–383. doi: 10.1016/s0014-4827(77)80044-x. [DOI] [PubMed] [Google Scholar]
  4. Cuatrecasas P. Gangliosides and membrane receptors for cholera toxin. Biochemistry. 1973 Aug 28;12(18):3558–3566. doi: 10.1021/bi00742a032. [DOI] [PubMed] [Google Scholar]
  5. Dessau W., Adelmann B. C., Timpl R. Identification of the sites in collagen alpha-chains that bind serum anti-gelatin factor (cold-insoluble globulin). Biochem J. 1978 Jan 1;169(1):55–59. doi: 10.1042/bj1690055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Engvall E., Ruoslahti E. Binding of soluble form of fibroblast surface protein, fibronectin, to collagen. Int J Cancer. 1977 Jul 15;20(1):1–5. doi: 10.1002/ijc.2910200102. [DOI] [PubMed] [Google Scholar]
  7. Engvall E., Ruoslahti E., Miller E. J. Affinity of fibronectin to collagens of different genetic types and to fibrinogen. J Exp Med. 1978 Jun 1;147(6):1584–1595. doi: 10.1084/jem.147.6.1584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fishman P. H., Brady R. O. Biosynthesis and function of gangliosides. Science. 1976 Nov 26;194(4268):906–915. doi: 10.1126/science.185697. [DOI] [PubMed] [Google Scholar]
  9. Fishman P. H., Brady R. O., Bradley R. M., Aaronson S. A., Todaro G. J. Absence of a specific ganglioside galactosyltransferase in mouse cells transformed by murine sarcoma virus. Proc Natl Acad Sci U S A. 1974 Feb;71(2):298–301. doi: 10.1073/pnas.71.2.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fishman P. H., Moss J., Osborne J. C., Jr Interaction of choleragen with the oligosaccharide of ganglioside GM1: evidence for multiple oligosaccharide binding sites. Biochemistry. 1978 Feb 21;17(4):711–716. doi: 10.1021/bi00597a024. [DOI] [PubMed] [Google Scholar]
  11. Gahmberg C. G., Hakomori S. Organization of glycolipids and glycoproteins in surface membranes: dependency on cell cycle and on transformation. Biochem Biophys Res Commun. 1974 Jul 10;59(1):283–291. doi: 10.1016/s0006-291x(74)80204-4. [DOI] [PubMed] [Google Scholar]
  12. Grinnell F. Cellular adhesiveness and extracellular substrata. Int Rev Cytol. 1978;53:65–144. doi: 10.1016/s0074-7696(08)62241-x. [DOI] [PubMed] [Google Scholar]
  13. Henneberry R. C., Fishman P. H., Freese E. Morphological changes in cultured mammalian cells: prevention by the calcium ionophore A23187. Cell. 1975 May;5(1):1–9. doi: 10.1016/0092-8674(75)90085-9. [DOI] [PubMed] [Google Scholar]
  14. Hollenberg M. D., Fishman P. H., Bennett V., Cuatrecasas P. Cholera toxin and cell growth: role of membrane gangliosides. Proc Natl Acad Sci U S A. 1974 Oct;71(10):4224–4228. doi: 10.1073/pnas.71.10.4224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hopper K. E., Adelmann B. C., Gentner G., Gay S. Recongnition by guinea-pig peritoneal exudate cells of conformationally different states of the collagen molecule. Immunology. 1976 Feb;30(2):249–259. [PMC free article] [PubMed] [Google Scholar]
  16. Huang R. T. Cell adhesion mediated by glycolipids. Nature. 1978 Dec 7;276(5688):624–626. doi: 10.1038/276624a0. [DOI] [PubMed] [Google Scholar]
  17. Hynes R. O. Alteration of cell-surface proteins by viral transformation and by proteolysis. Proc Natl Acad Sci U S A. 1973 Nov;70(11):3170–3174. doi: 10.1073/pnas.70.11.3170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Klebe R. J. Cell attachment to collagen: the requirement for energy. J Cell Physiol. 1975 Oct;86(2 Pt 1):231–236. doi: 10.1002/jcp.1040860206. [DOI] [PubMed] [Google Scholar]
  19. Klebe R. J. Isolation of a collagen-dependent cell attachment factor. Nature. 1974 Jul 19;250(463):248–251. doi: 10.1038/250248a0. [DOI] [PubMed] [Google Scholar]
  20. Kleinman H. K., McGoodwin E. B. Localization of the cell attachment region in types I and II collagens. Biochem Biophys Res Commun. 1976 Sep 20;72(2):426–432. doi: 10.1016/s0006-291x(76)80060-5. [DOI] [PubMed] [Google Scholar]
  21. Kleinman H. K., McGoodwin E. B., Martin G. R., Klebe R. J., Fietzek P. P., Woolley D. E. Localization of the binding site for cell attachment in the alpha1(I) chain of collagen. J Biol Chem. 1978 Aug 25;253(16):5642–5646. [PubMed] [Google Scholar]
  22. Langenbach R., Kennedy S. Gangliosides and their cell density-dependent changes in control and chemically transformed C3H/10T1/2 cells. Exp Cell Res. 1978 Mar 15;112(2):361–372. doi: 10.1016/0014-4827(78)90219-7. [DOI] [PubMed] [Google Scholar]
  23. Lingwood C. A., Hakomori S. Selective inhibition of cell growth and associated changes in glycolipid metabolism induced by monovalent antibodies to glycolipids. Exp Cell Res. 1977 Sep;108(2):385–391. doi: 10.1016/s0014-4827(77)80045-1. [DOI] [PubMed] [Google Scholar]
  24. Moss J., Fishman P. H., Manganiello V. C., Vaughan M., Brady R. O. Functional incorporation of ganglioside into intact cells: induction of choleragen responsiveness. Proc Natl Acad Sci U S A. 1976 Apr;73(4):1034–1037. doi: 10.1073/pnas.73.4.1034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Moss J., Manganiello V. C., Fishman P. H. Enzymatic and chemical oxidation of gangliosides in cultured cells: effects of choleragen. Biochemistry. 1977 May 3;16(9):1876–1881. doi: 10.1021/bi00628a018. [DOI] [PubMed] [Google Scholar]
  26. Pacuszka T., Duffard R. O., Nishimura R. N., Brady R. O., Fishman P. H. Biosynthesis of bovine thyroid gangliosides. J Biol Chem. 1978 Aug 25;253(16):5839–5846. [PubMed] [Google Scholar]
  27. Pearlstein E. Substrate activation of cell adhesion factor as a prerequisite for cell attachment. Int J Cancer. 1978 Jul 15;22(1):32–35. doi: 10.1002/ijc.2910220108. [DOI] [PubMed] [Google Scholar]
  28. Ruoslahti E., Vaheri A. Interaction of soluble fibroblast surface antigen with fribrinogen and fibrin. J Exp Med. 1975 Feb 1;141(2):497–501. doi: 10.1084/jem.141.2.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Vaheri A., Ruoslahti E. Fibroblast surface antigen produced but not retained by virus-transformed human cells. J Exp Med. 1975 Aug 1;142(2):530–535. doi: 10.1084/jem.142.2.530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Van Heyningen W. E., Carpenter C. C., Pierce N. F., Greenough W. B., 3rd Deactivation of cholera toxin by ganglioside. J Infect Dis. 1971 Oct;124(4):415–418. doi: 10.1093/infdis/124.4.415. [DOI] [PubMed] [Google Scholar]
  31. Veh R., Corfield A. P., Sander M., Schauer R. Neuraminic acid-specific modification and tritium labelling of gangliosides. Biochim Biophys Acta. 1976 Jan 18;486(1):145–160. doi: 10.1016/0005-2760(77)90079-0. [DOI] [PubMed] [Google Scholar]
  32. Yamada K. M., Kennedy D. W. Fibroblast cellular and plasma fibronectins are similar but not identical. J Cell Biol. 1979 Feb;80(2):492–498. doi: 10.1083/jcb.80.2.492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Yogeeswaran G., Hakomori S. Cell contact-dependent ganglioside changes in mouse 3T3 gibroblasts and a suppressed sialidase activity on cell contact. Biochemistry. 1975 May 20;14(10):2151–2156. doi: 10.1021/bi00681a017. [DOI] [PubMed] [Google Scholar]

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