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Identification and Pharmacological Characterization of a Specific Agmatine Transport System in Human Tumor Cell Lines
Author(s) -
MOLDERINGS GERHARD J.,
BRUSS MICHAEL,
BONISCH HEINZ,
GÖTHERT MANFRED
Publication year - 2003
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1304.008
Subject(s) - agmatine , chemistry , spermidine , putrescine , imidazoline receptor , biochemistry , idazoxan , pharmacology , biology , receptor , antagonist , prazosin , enzyme
A bstract : Specific accumulation of [ 14C ]agmatine in six human intestinal tumor cell lines and in the glioma cell line SK‐MG‐1 was inhibited by phentolamine, idazoxan, clonidine, 1,3‐di‐(2‐tolyl)guanidine, histamine, putrescine, spermine and spermidine. Corticosterone, desipramine, O‐methylisoprenaline, cirazoline, moxonidine, l‐arginine, l‐lysine, verapamil, nifedipine, CdCl 2 , ondansetron, and l‐carnitine failed to inhibit specific [ 14 C]agmatine accumulation, thus excluding that it is mediated by amino acid or monoamine carriers, by the putrescine carrier, by 5‐HT 3 receptor channels, by Ca 2+ channels or by the organic cation transporters OCT1, OCT2, OCT3, OCTN1, or OCTN2. This conclusion is supported by the finding that transfection of HEK293 cells with cDNA encoding either hOCT1, hOCT2, or hOCT3 did not enhance specific [ 14 C]agmatine accumulation compared to nontransfected cells. The data suggest that agmatine is accumulated by a specific agmatine transporter. Since incubation with exogenous agmatine for 24 hours increased intracellular agmatine content in all cell lines by a multiple of the basal endogenous content, the agmatine uptake system may be relevant for the regulation of the intra‐ and extracellular concentration of agmatine in humans.