The Preliminary Data show that the calcium-sensing receptor (CaR) suppresses parathyroid hormone-related protein (PTHrP) production by mammary epithelial cells (MEC) during lactation, and increases calcium (Ca) transport into milk. We will first use CaR-null mouse models to confirm these data. We will use graded dietary Ca restriction and calcimimetics to examine the CaR-mediated effects of systemic Ca on PTHrP production in the mammary glands (MG) of wild type mice, CaR mice, and CaR-/- mice made viable by the genetically engineered absence of parathyroid glands (CaR-/-/Gcm2-/-). We will also use this approach to study the regulation of MG Ca transport into milk by the CaR. We will examine the effect of extracellular Ca and calcimimetics on PTHrP production by MEC from these mice in culture, and characterize the signaling pathways, downstream from the CaR, that regulate PTHrP. Next, we will use three-dimensional cultures of primary MEC from the CaR-null mice, to examine the regulation of transepithelial Ca transport by the CaR, using a 45Ca tracer. We will also describe the signaling pathways that couple the CaR to Ca transport in MEC. Finally, in order to study the CaR's role in the MG during lactation on a backdrop of normal Ca metabolism, we will use the cre-lox system to delete the CaR specifically in the lactating MG. Using this model, we will study the role of the CaR in regulating PTHrP production, Ca transport, and milk production in the MG. We will also study systemic Ca and bone metabolism in these mice during lactation, as these are targets of mammary-derived PTHrP action. My career aim is to develop a research program at the intersection of Ca metabolism and MG biology that will lead to independence. In the short term, I would like to acquire skills in cell signaling and Ca imaging to complement my expertise in mammary gland biology. This will be accomplished through formal course work and by interactions with the co-sponsor and collaborators. Yale is an ideal training environment, with an abundance of physical and intellectual resources.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
5K01DK064206-03
Application #
7027655
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
2004-04-01
Project End
2007-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
3
Fiscal Year
2006
Total Cost
$112,282
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
VanHouten, Joshua N; Neville, Margaret C; Wysolmerski, John J (2007) 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. Endocrinology 148:5943-54
VanHouten, Joshua N; Yu, Namyi; Rimm, David et al. (2006) Hypercalcemia of malignancy due to ectopic transactivation of the parathyroid hormone gene. J Clin Endocrinol Metab 91:580-3
Ardeshirpour, Laleh; Dann, Pamela; Pollak, Martin et al. (2006) The calcium-sensing receptor regulates PTHrP production and calcium transport in the lactating mammary gland. Bone 38:787-93
VanHouten, Joshua N (2005) Calcium sensing by the mammary gland. J Mammary Gland Biol Neoplasia 10:129-39