Role of carbohydrates in rat leukemia cell‐liver macrophage cell contacts
- 1 January 1985
- journal article
- research article
- Published by Wiley in Biology of the Cell
- Vol. 52 (3), 253-258
- https://doi.org/10.1111/j.1768-322x.1985.tb00344.x
Abstract
The mechanism by which macrophages recognize tumor cells is still unknown. Interactions were studied between rat liver macrophages and rat L-5222 leukemia cells. These tumor cells, but not normal leukocytes or erythrocytes, adhere to freshly isolated macrophages in vitro. Binding of tumor cells by macrophages can be inhibited by N-acetyl-D-galactosamine, D-galactose and more potently by glycoproteins with terminal N-acetyl-D-galactosamine or D-galactose residues. Tumor cell adhesion is Ca-dependent. The relevant leukemia cell membrane structures which bear terminal .beta.-D-galactosyl or related residues were determined as trypsin- and pronase-sensitive, and hence may presumably be glycoproteins. The tumor cell receptor on liver macrophages appears to be a lectin with the carbohydrate specificity N-acetyl-D-galactosamine > D-galactose > L-fucose.This publication has 4 references indexed in Scilit:
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