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钙敏感受体调节乳腺上皮细胞中的质膜钙三磷酸腺苷酶同工型2活性:一种钙调节钙转运至乳汁中的机制。

The calcium-sensing receptor regulates plasma membrane calcium adenosine triphosphatase isoform 2 activity in mammary epithelial cells: a mechanism for calcium-regulated calcium transport into milk.

作者信息

VanHouten Joshua N, Neville Margaret C, Wysolmerski John J

机构信息

Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520-8020, USA.

出版信息

Endocrinology. 2007 Dec;148(12):5943-54. doi: 10.1210/en.2007-0850. Epub 2007 Sep 6.

Abstract

The calcium-sensing receptor (CaR) regulates transepithelial calcium transport into milk by mammary epithelial cells. Using a genome-wide screening strategy, we identified the plasma membrane calcium ATPase isoform 2 (PMCA2) as a potential downstream target of the CaR. We show that PMCA2 expression in the mouse mammary gland increases during lactation and that PMCA2 is localized solely to the apical plasma membrane of mammary epithelial cells. In milk from deafwaddler mice, which have mutations in the gene encoding PMCA2, calcium concentrations were reduced, confirming its importance in calcium transport into milk. Furthermore, in cultured primary and EpH4 mouse mammary epithelial cells, CaR stimulation up-regulated calcium-dependent ATPase activity in plasma membrane preparations. By small interfering RNA-mediated gene knockdown of PMCA2, we show that PMCA2 accounts for the preponderance of calcium-ATPase activity. We also show that reduction of CaR expression with small interfering RNA eliminates the ability of extracellular calcium to elicit an increase in calcium-dependent ATPase activity in EpH4 cell membranes. These results demonstrate that activation of the CaR increases PMCA2 activity in mouse mammary epithelial cells, providing a mechanism for the regulation of transepithelial calcium transport by calcium in the lactating mouse mammary gland.

摘要

钙敏感受体(CaR)调节乳腺上皮细胞跨上皮钙转运进入乳汁的过程。利用全基因组筛选策略,我们鉴定出质膜钙ATP酶同工型2(PMCA2)是CaR的一个潜在下游靶点。我们发现,小鼠乳腺中PMCA2的表达在哺乳期增加,且PMCA2仅定位于乳腺上皮细胞的顶端质膜。在编码PMCA2的基因发生突变的聋摇小鼠的乳汁中,钙浓度降低,证实了其在钙转运进入乳汁中的重要性。此外,在原代培养的和EpH4小鼠乳腺上皮细胞中,CaR刺激上调了质膜制剂中钙依赖性ATP酶的活性。通过小干扰RNA介导的PMCA2基因敲低,我们发现PMCA2占钙ATP酶活性的绝大部分。我们还发现,用小干扰RNA降低CaR表达可消除细胞外钙引起EpH4细胞膜中钙依赖性ATP酶活性增加的能力。这些结果表明,CaR的激活增加了小鼠乳腺上皮细胞中PMCA2的活性,为哺乳期小鼠乳腺中钙调节跨上皮钙转运提供了一种机制。

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