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Endocrinology, doi:10.1210/en.2007-0850
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Endocrinology Vol. 148, No. 12 5943-5954
Copyright © 2007 by The Endocrine Society

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

Joshua N. VanHouten, Margaret C. Neville and John J. Wysolmerski

Department of Internal Medicine (J.N.V., J.J.W.), Division of Endocrinology and Metabolism, Yale University School of Medicine, New Haven, Connecticut 06520; and Department of Physiology and Biophysics (M.C.N.), University of Colorado Health Science Center at Fitzsimons, Aurora, Colorado 80045

Address all correspondence and requests for reprints to: John Wysolmerski, M.D., Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University School of Medicine, PO Box 208020, New Haven, Connecticut 06520-8020. E-mail: john.wysolmerski{at}yale.edu.

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.




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