Abstract
Purpose. Taurine, a β-amino acid, is a neuromodulator which interacts functionally with the glycinergic, GABAergic, cholinergic and adrenergic systems. Although a continuous cell culture model is not available for the choroid plexus epithelia, we recently described a primary cell culture of rabbit choroid plexus epithelia. The goal of the current study was to determine the suitability of this primary cell culture for the study of the Na+-taurine transporter in the rabbit choroid plexus.
Methods. A primary cell culture of rabbit choroid plexus epithelial cells was grown on semi-permeable filters and kinetics of 3H-taurine uptake were ascertained.
Results. Taurine transport in the cultured choroid plexus cells was Na+-dependent and saturable (Km = 156 μM). The β-amino acids, β-alanine and taurine, significantly inhibited Na+-driven taurine transport whereas L-alanine partially inhibited taurine transport in the cultured cells. In addition, we observed that the activity of the Na+-taurine transporter is affected by exposure to taurine in the media.
Conclusions. These results demonstrate that a Na+-taurine transporter with characteristics similar to those in the intact tissue is expressed in cultured choroid plexus epithelial cells. The transporter may undergo adaptive regulation and play a role in taurine homeostasis in the central nervous system.
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Ramanathan, V.K., Chung, SJ., Giacomini, K.M. et al. Taurine Transport in Cultured Choroid Plexus. Pharm Res 14, 406–409 (1997). https://doi.org/10.1023/A:1012074827388
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DOI: https://doi.org/10.1023/A:1012074827388