The goal of this Program Project is to elucidate the hormonal, molecular, and cellular mechanisms involved in two critical developmental transitions in the mammary gland: those from pregnancy to lactation, and from lactation to the return of the lactating gland to its pre-pregnant state at involution. The proposed research is designed to provide an integrated and cooperative approach to these problems. In Project I, the relationship between progesterone withdrawal and tight junction closure during the transition between pregnancy and lactation will be examined using state of the art genomic and proteomic technology. In Project II the detailed molecular mechanisms by which progesterone inhibits milk secretion during pregnancy will be elucidated focusing on interactions between the progesterone receptor, the glucocorticoid receptor and the JAK/STAT signal transduction pathway. In Project III the molecules that regulate the physical expansion of the Golgi and the onset of mil lipid secretion during the transition to lactation will be identified and their functional significance assessed. Finally, in Project IV the mechanisms by which mammary epithelial cells and macrophages remove apoptotic cells from the involuting mammary gland in the absence of inflammation will be studied. Three cores will provide (A) administrative support, (B) specialized animal breeding and surgical support and (C) adenovirus vectors for use in transduction of genes designed to alter functional pathways. Experiments will be carried out in vitro and in vivo using advanced techniques to examine changes in gene expression and protein composition during these well-define developmental transitions of the epithelium from one physiological state to another. These studies should enhance our understanding of developmental and secretory regulation in the mammary gland and provide an excellent model for the regulation of similar processes in many organs. Because milk is critically important to infant nutrition, better insight into these transitions should lead to improve infant nutrition as well as contribute to the prevention and cure of breast diseases.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
1P01HD038129-01A1
Application #
6190807
Study Section
Special Emphasis Panel (ZHD1-MCHG-B (MN))
Program Officer
Grave, Gilman D
Project Start
2000-08-23
Project End
2005-05-31
Budget Start
2000-08-23
Budget End
2001-05-31
Support Year
1
Fiscal Year
2000
Total Cost
$899,857
Indirect Cost
Name
University of Colorado Denver
Department
Physiology
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Rudolph, Michael C; Jackman, Matthew R; Presby, David M et al. (2018) Low Neonatal Plasma n-6/n-3 PUFA Ratios Regulate Offspring Adipogenic Potential and Condition Adult Obesity Resistance. Diabetes 67:651-661
Checkley, L Allyson; Rudolph, Michael C; Wellberg, Elizabeth A et al. (2017) Metformin Accumulation Correlates with Organic Cation Transporter 2 Protein Expression and Predicts Mammary Tumor RegressionIn Vivo. Cancer Prev Res (Phila) 10:198-207
Rudolph, M C; Young, B E; Lemas, D J et al. (2017) Early infant adipose deposition is positively associated with the n-6 to n-3 fatty acid ratio in human milk independent of maternal BMI. Int J Obes (Lond) 41:510-517
Baumgartner, Heidi K; Rudolph, Michael C; Ramanathan, Palaniappian et al. (2017) Developmental Expression of Claudins in the Mammary Gland. J Mammary Gland Biol Neoplasia 22:141-157
Heinz, Richard E; Rudolph, Michael C; Ramanathan, Palani et al. (2016) Constitutive expression of microRNA-150 in mammary epithelium suppresses secretory activation and impairs de novo lipogenesis. Development 143:4236-4248
Grimm, Sandra L; Hartig, Sean M; Edwards, Dean P (2016) Progesterone Receptor Signaling Mechanisms. J Mol Biol 428:3831-49
TreviƱo, Lindsey S; Bolt, Michael J; Grimm, Sandra L et al. (2016) Differential Regulation of Progesterone Receptor-Mediated Transcription by CDK2 and DNA-PK. Mol Endocrinol 30:158-72
Sladek, Celia D; Stevens, Wanida; Song, Zhilin et al. (2016) The ""metabolic sensor"" function of rat supraoptic oxytocin and vasopressin neurons is attenuated during lactation but not in diet-induced obesity. Am J Physiol Regul Integr Comp Physiol 310:R337-45
Libby, Andrew E; Bales, Elise; Orlicky, David J et al. (2016) Perilipin-2 Deletion Impairs Hepatic Lipid Accumulation by Interfering with Sterol Regulatory Element-binding Protein (SREBP) Activation and Altering the Hepatic Lipidome. J Biol Chem 291:24231-24246
Rudolph, Michael C; Young, Bridget E; Jackson, Kristina Harris et al. (2016) Human Milk Fatty Acid Composition: Comparison of Novel Dried Milk Spot Versus Standard Liquid Extraction Methods. J Mammary Gland Biol Neoplasia 21:131-138

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