The purpose of this project is to allow the principal investigator time to gain a through training in basic medical research so that he can become a productive independent investigator with special interests in the prolactin isoforms. The training phase includes 1) course work and seminars in molecular biology, cell biology, endocrinology, protein biochemistry, and correlations between basic medical research and clinical practice; 2) laboratory training in cell culture, protein isolation, protein iodnation, bio- and radioimmunoassay of hormone, and monoclonal antibody development. The principal investigator also expects to complete two preprojects during this phase: 1) large scale isolation of each of the isoforms of prolactin, and 2) the thorough characterizaton of quantitative assays for them. In the second phase of this project, the principal investigator will apply what he has learned in the first phase to study 1) the distribution of the different isoforms of prolactin in different physiological and pathological conditions; 2) the effect of nutritional factors on the regulation of secretion of the isoforms; 3) the relationship between these monomeric isoforms and the clinically studied oligomeric prolactins; and 4) the possible different roles of the isoforms in lactotroph autoregulation. Phase I will be under the co- sponsorship of Dr. Ameae Walker, whose area of research is prolactin endocrinology, and Dr. Richard Luben, whose research focuses on the mechanism of hormone action. Phase II will continue to include guidance from Drs. Walker and Luben, but will also include additional input from Dr. Anthony Norman, whose area of research includes effects of nutritional factors, most particularly vitamin D, on hormone regulation. Promotion from phase I to II will be a committee decision based on course and laboratory performance and the production of a comprehensive research proposal for phase II.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Physician Scientist Award (K11)
Project #
5K11HD000810-04
Application #
3086984
Study Section
Maternal and Child Health Research Committee (HDMC)
Project Start
1987-09-01
Project End
1992-08-31
Budget Start
1990-09-01
Budget End
1991-08-31
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Type
Schools of Medicine
DUNS #
City
Riverside
State
CA
Country
United States
Zip Code
92521
Johnson, Terence E; Vue, Mayza; Brekhus, Sharyn et al. (2003) Unmodified prolactin (PRL) promotes PRL secretion and acidophil hypertrophy and is associated with pituitary hyperplasia in female rats. Endocrine 20:101-10
Walker, A M; Montgomery, D W; Saraiya, S et al. (1995) Prolactin-immunoglobulin G complexes from human serum act as costimulatory ligands causing proliferation of malignant B lymphocytes. Proc Natl Acad Sci U S A 92:3278-82
Ho, T W; Leong, F S; Olaso, C H et al. (1993) Secretion of specific nonphosphorylated and phosphorylated rat prolactin isoforms at different stages of the estrous cycle. Neuroendocrinology 58:160-5
Walker, A M; Peabody, C A; Ho, T W et al. (1992) 50 kD prolactin binding protein in schizophrenics on neuroleptic medication. J Psychiatry Neurosci 17:61-7
Krown, K A; Wang, Y F; Ho, T W et al. (1992) Prolactin isoform 2 as an autocrine growth factor for GH3 cells. Endocrinology 131:595-602
Ho, T W; Balden, E; Chao, J et al. (1991) Prolactin (PRL) processing by kallikrein: production of the 21-23.5K PRL-like molecules and inferences about PRL storage in mature secretory granules. Endocrinology 129:184-92
Ho, T W; Greenan, J R; Walker, A M (1989) Mammotroph autoregulation: the differential roles of the 24K isoforms of prolactin. Endocrinology 124:1507-14
Greenan, J R; Balden, E; Ho, T W et al. (1989) Biosynthesis of the secreted 24 K isoforms of prolactin. Endocrinology 125:2041-8