Abstract
Normal and neoplastic cells from 4 species (man, rat, mouse and hamster) were examined for their dependence on exogenous L-arginine in tissue culture. The malignant cells required a higher concentration of L-arginine in the medium than their normal counterparts (with similar doubling times) to maintain optimal proliferation. Complete arginine deprivation resulted in equal growth inhibition of normal and malignant cells, but more rapid cytolysis of the malignant cell. Deprivation of L-arginine, followed 24 h later by rescue with L-arginine, allowed normal cells to proliferate, but the reproductive capacity of the malignant cells was irreversibly impaired. Since the cytotoxic activity of LPS-activated macrophages was associated with the release of arginase and was abrogated by excess L-arginine, it is suggested that the biological basis for the selective effects of such macrophages may reside in the L-arginine dependence of the target cells.
MeSH Terms
Animals
Arginase/metabolism
Arginine/metabolism,pharmacology
Cell Count
Cell Survival/drug effects
Cells, Cultured
Cricetinae
Cytotoxicity, Immunologic/drug effects
Humans
Macrophages/enzymology,immunology,metabolism
Mice
Neoplasms, Experimental/immunology,metabolism
Rats
Chemicals
Arginine
Arginase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Currie G A
Basham C
References (12)
12 references, click to expand
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