In light of the ability of CRH-BP to antagonize the biological activity of CRH in vitro, it is hypothesized that the CRH-BP modulates the actions of CRH in the pituitary and central nervous system. This hypothesis is tested by several independent approaches presented in this proposal. First, in situ hybridization histochemistry, immunocytochemistry, and RNase protection assays will be utilized to characterize the in vivo regulation of CRH-BP expression within the HPA axis during development and in response to glucocorticoids and stress, two important modulators of CRH expression and HPA activity. The expression and regulation of CRH-BP will also be examined in CRH-deficient mice. Second, the physiological consequences of increased level of CRH-BP in the anterior pituitary will be assessed in a transgenic mouse model of anterior pituitary CRH-BP overexpression. Third, the physiological consequences of decreased CRH-BP levels will be determined in a mammalian model of CRH-BP deficiency created by targeted mutation of the CRH-BP gene in embryonic stem cells. Together, these studies should allow the investigators to elucidate the physiological role of the CRH-BP in pituitary and brain. Finally, studies on the molecular characterization of CRH-BP gene regulation will be initiated in a number of CRH-BP expressing cell lines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK042730-09S1
Application #
6340146
Study Section
Endocrinology Study Section (END)
Program Officer
Sato, Sheryl M
Project Start
1990-12-01
Project End
2001-06-30
Budget Start
2000-07-01
Budget End
2001-06-30
Support Year
9
Fiscal Year
2000
Total Cost
$86,514
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Biochemistry
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Stinnett, Gwen S; Westphal, Nicole J; Seasholtz, Audrey F (2015) Pituitary CRH-binding protein and stress in female mice. Physiol Behav 150:16-23
Ketchesin, Kyle D; Seasholtz, Audrey F (2015) Novel Roles for CRF-Binding Protein and CRF Receptor 2 in Binge Drinking. Alcohol Clin Exp Res 39:2296-8
Westphal, Nicole J; Evans, Ryan T; Seasholtz, Audrey F (2009) Novel expression of type 1 corticotropin-releasing hormone receptor in multiple endocrine cell types in the murine anterior pituitary. Endocrinology 150:260-7
Seasholtz, Audrey F; Ohman, Miina; Wardani, Amale et al. (2009) Corticotropin-releasing hormone receptor expression and functional signaling in murine gonadotrope-like cells. J Endocrinol 200:223-32
Evans, Ryan T; Seasholtz, Audrey F (2009) Soluble corticotropin-releasing hormone receptor 2alpha splice variant is efficiently translated but not trafficked for secretion. Endocrinology 150:4191-202
Karolyi, I J; Burrows, H L; Ramesh, T M et al. (1999) Altered anxiety and weight gain in corticotropin-releasing hormone-binding protein-deficient mice. Proc Natl Acad Sci U S A 96:11595-600
Burrows, H L; Nakajima, M; Lesh, J S et al. (1998) Excess corticotropin releasing hormone-binding protein in the hypothalamic-pituitary-adrenal axis in transgenic mice. J Clin Invest 101:1439-47