Abstract
Summary
The incorporation and fate of heparin in L, LE, Hela, and mouse embryo tissue culture cells was studied. The results were as follows: (a) heparin at the concentrations used had a stimulatory effect of about 15% in the cell growth; (b) incorporation of heparin in L, LE, and Hela cells was in the order of 1 μg of heparin/million cells and in the mouse embryo cells in the order of 12–20 μg/million cells; (c) analysis by chromatography and electrophoresis of radioactive material incorporated or released after incubation with heparin of the four cell lines revealed that no degradation of the compound occurred; (d) microscopic observations indicated that heparin is deposited in the cells in the form of granules; (e) the incorporation of heparin by the cells was increased by puromycin and actinomycin and was not affected by mitomycin. A possible mechanism by which heparin penetrates and is excreted by the cells is discussed.
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