Prolactinomas are the most common pituitary adenomas, occurring primarily in women of reproductive age. Manifestations of hyperprolactinemia include infertility in women and impotence in men. Estrogens stimulate prolactin gene expression and release, and promote lactotroph proliferation, but their role in the development of prolactinomas remain unclear. The recent discovery of estrogen receptor variants and a novel estrogen receptor raises questions regarding their presence and function in human prolactinomas. We recently identified two distinct cell populations in human prolactinoma cell cultures. The majority of cells are lactotrophs, as evident by their expression and release of prolactin. These cells also express estrogen receptors. A morphologically distinct subpopulation of cells produces prolactin regulating factor (PRF), as judged by increased prolactin gene expression in cocultured rat lactotrophs. It is our hypothesis that different forms of the estrogen receptor and/or a subpopulation of PRF-producing cells support the development of human prolactinomas. Our objectives are to: a) characterize estrogen receptors and estrogenic actions in cultured human prolactinoma cells, b) investigate PRF-producing cells in these cultures, c) establish a human prolactinoma cell line. This research will help to understand the etiology of human prolactinomas.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31DK009652-01
Application #
2395325
Study Section
Special Emphasis Panel (ZRG2-PSF (02))
Program Officer
Hyde, James F
Project Start
1998-04-05
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Takayanagi, Takehiko; Forrester, Steven J; Kawai, Tatsuo et al. (2016) Vascular ADAM17 as a Novel Therapeutic Target in Mediating Cardiovascular Hypertrophy and Perivascular Fibrosis Induced by Angiotensin II. Hypertension 68:949-955
Ochoa, A L; Mitchner, N A; Paynter, C D et al. (2000) Vascular endothelial growth factor in the rat pituitary: differential distribution and regulation by estrogen. J Endocrinol 165:483-92