Estrogen regulation and ion dependence of taurine uptake by MCF-7 human breast cancer cells.

Cell Mol Biol Lett

Strathclyde Institute of Pharmacy and Biomedical Sciences, Royal College, University of Strathclyde, 204 George Street, Glasgow, UK. G1 1XW,

Published: September 2007

It has been reported that estrogen receptor-positive MCF-7 cells express TauT, a Na(+)-dependent taurine transporter. However, there is a paucity of information relating to the characteristics of taurine transport in this human breast cancer cell line. Therefore, we have examined the characteristics and regulation of taurine uptake by MCF-7 cells. Taurine uptake by MCF-7 cells showed an absolute dependence upon extracellular Na(+). Although taurine uptake was reduced in Cl(-) free medium a significant portion of taurine uptake persisted in the presence of NO(3) (-). Taurine uptake by MCF-7 cells was inhibited by extracellular beta-alanine but not by L-alanine or L-leucine. 17β-estadiol increased taurine uptake by MCF-7 cells: the V(max) of influx was increased without affecting the K(m). The effect of 17β-estradiol on taurine uptake by MCF-7 cells was dependent upon the presence of extracellular Na(+). In contrast, 17β-estradiol had no significant effect on the kinetic parameters of taurine uptake by estrogen receptor-negative MDA-MB-231 cells. It appears that estrogen regulates taurine uptake by MCF-7 cells via TauT. In addition, Na(+)-dependent taurine uptake may not be strictly dependent upon extracellular Cl(-).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275591PMC
http://dx.doi.org/10.2478/s11658-007-0011-4DOI Listing

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