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Na + ‐Dependent Uptake and Release of Taurine by Neuroblastoma × Glioma Hybrid Cells
Author(s) -
Kürzinger Konrad,
Hamprecht Bernd
Publication year - 1981
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1981.tb04483.x
Subject(s) - taurine , hypotaurine , extracellular , cytosol , intracellular , chemistry , biochemistry , biophysics , biology , amino acid , enzyme
In neuroblastoma × glioma hybrid cells, a cell line of neuronal character, a saturable uptake system for taurine is found which displays high affinity and high capacity ( K m = 38 μ m , V = 1.25 nmol mg −1 min −1 )‐ Only the closely related structural analogues hypotaurine and β‐alanine are able to inhibit the transport of radioactively labeled taurine. Imipramine or haloperidol at 100 μ m effectively blocks taurine uptake. High‐affinity taurine uptake shows an absolute and highly specific requirement for Na + . The hybrid cells internalize taurine very slowly and, with 1 m m extracellular taurine, attain a plateau only after more than 20 h, at which time approximately 34 m m labeled taurine has accumulated in the cytosol. Generally there is hardly any spontaneous release of accumulated taurine. Efflux can, however, be induced by increasing the intracellular Na + content and is then accelerated by lowering the extracellular Na + concentration. The hypothesis is forwarded that taurine may exert its function by driving the extrusion of Na + in emergency situations.