Blocking of lectin-like adhesion molecules on pulmonary cells inhibits lung sarcoma L-1 colonization in BALB/c-mice |
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Authors: | W. Roszkowski J. Beuth H. L. Ko G. Uhlenbruck G. Pulverer |
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Affiliation: | (1) National Institute of Lung Diseases and Tuberculosis, Warsaw, Poland;(2) Institute of Hygiene, University of Cologne, Goldenfelsstrasse 19–21, D-5000 Cologne, Germany;(3) Institute of Immunobiology, University of Cologne, D-5000 Cologne, Germany |
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Abstract: | Summary Adhesion and inhibition experiments with pulmonary cells of BALB/c-mouse origin and syngeneic sarcoma L-1 cells indicated that L-fucose specific lectin-like adhesion molecules, presumably situated on pulmonary cell surfaces are (at least partly) responsible for the specificity of this cell-cell interaction. Addition of specific sugars and glycoconjugates (L-fucose and fucoidan, respectively) to the incubation medium evidently inhibited the adhesion process as quantified using radiolabelled tumor cells. Unspecific carbohydrates (e.g. D-galactose) did not affect the cellular interaction. In vivo, repeated administration of fucoidan (but not of unspecific glycoconjugates) significantly inhibited the settling of metastatic sarcoma L-1 cells in the lungs of BALB/c-mice. Therefore, when lectin-like adhesion molecules on pulmonary cells were blocked with competitive glycoconjugates, tumor cell colonization of the lung could be significantly inhibited. |
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Keywords: | Glycoprotein sarcoma L-1 tumor cells L-fucose fucoidan lung metastasis BALB/c-mice |
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