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雌二醇调控 MCF-7 人乳腺癌细胞牛磺酸摄取的离子依赖性

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

机构信息

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

出版信息

Cell Mol Biol Lett. 2007 Sep;12(3):396-406. doi: 10.2478/s11658-007-0011-4. Epub 2007 Mar 3.

Abstract

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(-).

摘要

据报道,雌激素受体阳性 MCF-7 细胞表达 TauT,一种 Na(+)-依赖性牛磺酸转运体。然而,关于这种人乳腺癌细胞系中牛磺酸转运的特征,信息仍然很少。因此,我们研究了 MCF-7 细胞中牛磺酸摄取的特征和调节。MCF-7 细胞摄取牛磺酸绝对依赖于细胞外 Na(+)。虽然在无 Cl(-)的培养基中,牛磺酸摄取减少,但在存在 NO(3) (-)的情况下,仍有很大一部分牛磺酸摄取持续存在。MCF-7 细胞摄取牛磺酸被细胞外 β-丙氨酸抑制,但不受 L-丙氨酸或 L-亮氨酸抑制。17β-雌二醇增加 MCF-7 细胞的牛磺酸摄取:流入的 V(max)增加,而不影响 K(m)。17β-雌二醇对 MCF-7 细胞牛磺酸摄取的影响依赖于细胞外 Na(+)的存在。相比之下,17β-雌二醇对雌激素受体阴性 MDA-MB-231 细胞牛磺酸摄取的动力学参数没有显著影响。雌激素似乎通过 TauT 调节 MCF-7 细胞的牛磺酸摄取。此外,Na(+)-依赖性牛磺酸摄取可能不完全依赖于细胞外 Cl(-)。

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