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. 1977 Nov;30(2):323–329.

Non-specific recognition mechanisms by mononuclear phagocytes.

D M Weir, H M Ogmundsdóttir
PMCID: PMC1541108  PMID: 606447

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Selected References

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

  1. Arend W. P., Mannik M. The macrophage receptor for IgG: number and affinity of binding sites. J Immunol. 1973 Jun;110(6):1455–1463. [PubMed] [Google Scholar]
  2. Dawes J., Tuach S. J., McBride W. H. Properties of an antigenic polysaccharide from Corynebacterium parvum. J Bacteriol. 1974 Oct;120(1):24–30. doi: 10.1128/jb.120.1.24-30.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Deman J. J., Vakaet L. C., Bruyneel E. A. Cell size and mutual cell adhesion. II. Evidence for a relation between cell size, long-range electrostatic repulsion and intercellular adhesiveness during density-regulated growth in suspension. J Membr Biol. 1976 Mar 18;26(2-3):205–215. doi: 10.1007/BF01868874. [DOI] [PubMed] [Google Scholar]
  4. Ghaffar A., Cullen R. T., Dunbar N., Woodruff M. F. Anti-tumour effect in vitro of lymphocytes and macrophages from mice treated with Corynebacterium parvum. Br J Cancer. 1974 Mar;29(3):199–205. doi: 10.1038/bjc.1974.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hakomori S. I., Murakami W. T. Glycolipids of hamster fibroblasts and derived malignant-transformed cell lines. Proc Natl Acad Sci U S A. 1968 Jan;59(1):254–261. doi: 10.1073/pnas.59.1.254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Jones J. T., McBride W. H., Weir D. M. The in vitro killing of syngeneic cells by peritoneal cells from adjuvant-stimulated mice. Cell Immunol. 1975 Aug;18(2):375–383. doi: 10.1016/0008-8749(75)90066-0. [DOI] [PubMed] [Google Scholar]
  7. Keller R. Major changes in lymphocyte proliferation evoked by activated macrophages. Cell Immunol. 1975 Jun;17(2):542–551. doi: 10.1016/s0008-8749(75)80058-x. [DOI] [PubMed] [Google Scholar]
  8. LaMont J. T., Gammon M. T., Isselbacher K. J. Cell-surface glycosyltransferases in cultured fibroblasts: increased activity and release during serum stimulation of growth. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1086–1090. doi: 10.1073/pnas.74.3.1086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Leu R. W., Eddleston A. L., Hadden J. W., Good R. A. Mechanism of action of migration inhibitory factor (MIF). I. Evidence for a receptor for MIF present on the peritoneal macrophage but not on the alveolar macrophage. J Exp Med. 1972 Sep 1;136(3):589–603. doi: 10.1084/jem.136.3.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lunney J., Ashwell G. A hepatic receptor of avian origin capable of binding specifically modified glycoproteins. Proc Natl Acad Sci U S A. 1976 Feb;73(2):341–343. doi: 10.1073/pnas.73.2.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nicolson G. L., Poste G. The cancer cell: dynamic aspects and modifications in cell-surface organization (first of two parts). N Engl J Med. 1976 Jul 22;295(4):197–203. doi: 10.1056/NEJM197607222950405. [DOI] [PubMed] [Google Scholar]
  12. Nir S., Andersen M. Van der Waals interactions between cell surfaces. J Membr Biol. 1977 Feb 24;31(1-2):1–18. doi: 10.1007/BF01869396. [DOI] [PubMed] [Google Scholar]
  13. Ogmundsdóttir H. M., Weir D. M. The characteristics of binding of Corynebacterium parvum to glass-adherent mouse peritoneal exudate cells. Clin Exp Immunol. 1976 Nov;26(2):334–339. [PMC free article] [PubMed] [Google Scholar]
  14. Remold H. G. Requirement for alpha-L-fucose on the macrophage membrane receptor for MIF. J Exp Med. 1973 Nov 1;138(5):1065–1076. doi: 10.1084/jem.138.5.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Roseman S. The synthesis of complex carbohydrates by multiglycosyltransferase systems and their potential function in intercellular adhesion. Chem Phys Lipids. 1970 Oct;5(1):270–297. doi: 10.1016/0009-3084(70)90024-1. [DOI] [PubMed] [Google Scholar]
  16. Roth S., McGuire E. J., Roseman S. Evidence for cell-surface glycosyltransferases. Their potential role in cellular recognition. J Cell Biol. 1971 Nov;51(21):536–547. doi: 10.1083/jcb.51.2.536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sharon N., Lis H. Lectins: cell-agglutinating and sugar-specific proteins. Science. 1972 Sep 15;177(4053):949–959. doi: 10.1126/science.177.4053.949. [DOI] [PubMed] [Google Scholar]
  18. Stossel T. P. Phagocytosis: recognition and ingestion. Semin Hematol. 1975 Jan;12(1):83–116. [PubMed] [Google Scholar]
  19. Stossel T. P. Quantitative studies of phagocytosis. Kinetic effects of cations and heat-labile opsonin. J Cell Biol. 1973 Aug;58(2):346–356. doi: 10.1083/jcb.58.2.346. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Wilkinson P. C. Recognition and response in mononuclear and granular phagocytes. Clin Exp Immunol. 1976 Sep;25(3):355–366. [PMC free article] [PubMed] [Google Scholar]
  21. Woodruff J. J., Gesner B. M. The effect of neuraminidase on the fate of transfused lymphocytes. J Exp Med. 1969 Mar 1;129(3):551–567. doi: 10.1084/jem.129.3.551. [DOI] [PMC free article] [PubMed] [Google Scholar]

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