Abstract
A highly lung-colonizing cell line RMS/82 was obtained by DNA transfection from a low lung-colonizing line RMS/8, a clone of a rat rhabdomyosarcoma cell line. The cells were metabolically labeled with3H-glucosamine and35S-sulfate. The newly synthesized pericellular glycosaminoglycans and the ability of the cells from the two lines to degrade extracellular matrix components were studied comparatively. The following conclusions were obtained: 1) Thein vitro proliferation rate is not a determinant in the modulation of the colonizing potential of these cells; 2) The strongly colonizing RMS/82 cells release more radioactivity from the radiolabeled extracellular matrix than their weakly colonizing counterparts; 3) The cells with a high colonizing potential incorporated less radioactivity into the cell surface glycosaminoglycans, and exhibited a lower heparan sulfate to chondroitin sulfate ratio than the weakly colonizing RMS/8 line.
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Abbreviations
- RMS:
-
rhabdomyosarcoma
- ECM:
-
extracellular matrix
- GAGs:
-
glycosaminoglycans
- DMEM:
-
Dulbecco's modified essential medium
- FCS:
-
fetal calf serum
- PBS:
-
phosphate buffered saline
- CPC:
-
cetylpyridinium chloride
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Redini, F., Verrelle, P., Hillova, J. et al. Cell surface glycosaminoglycans of a tumor cell line and its DNA transfected variant differing in their lung colonizing potential. Glycoconjugate J 4, 191–201 (1987). https://doi.org/10.1007/BF01049456
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DOI: https://doi.org/10.1007/BF01049456