This continuation proposal requests support for the Molecular Endocrinology Training Program (METP) at Vanderbilt University Medical Center (VUMC). Thirty nine faculty members in the departments of Biochemistry, Cancer Biology, Cell and Developmental Biology, Microbiology and Immunology, Molecular Physiology and Biophysics, Pathology and Pharmacology constitute the preceptors of the METP. Of this group thirty four are established faculty with stable, well-funded programs and training experience and five are new investigators; given our Institutional recruiting plans, several more appointments at both junior and senior levels will be made in the next few years. The preceptor group constitutes an unusually diverse and talented group of individuals whose work covers the spectrum of molecular endocrinology. These preceptors conduct research in the general areas of: 1) signal transduction 2) the hormonal regulation of gene expression 3) metabolic regulation and 4) beta cell development and function. The request for a steady state level of 10 predoctoral and 4 postdoctoral trainees is justified on the basis of the number, size and quality of the research programs directed by the preceptors and the Institutional commitment to expanding the recruitment of trainees. All METP trainees are appointed upon the advice of an Advisory Committee after being nominated by a preceptor. Postdoctoral trainees have a Ph.D. or M.D. degree or both. Rigorous in-depth research training is the focus of both the pre- and postdoctoral training programs. However, the METP also ensures that all trainees receive a broad didactic education through courses in Molecular Endocrinology and Metabolic Regulation. In addition, all METP trainees attend the Vanderbilt Diabetes Center (VDC) seminar series and meet with the visiting scientists. The Program also provides formal training in the proper use of radioisotopes, in appropriate procedures of dealing with toxic and dangerous materials, and in the responsible conduct in research METP trainees also have access to a formal career counseling program to deal with matters that concern employment opportunities. Predoctoral training in the METP follows that received in the Interdisciplinary Graduate Program in Biomedical Sciences (IGP). The IGP recruits all predoctoral trainees in the biomedical sciences at Vanderbilt and provides a first year core curriculum. It also supervises laboratory rotations and preceptor selection among the participating eight Departments. This centralized recruitment has considerably increased the number and quality of students that enter Vanderbilt and subsequently compete for METP support. Quality is assessed on the basis of GPA and GRE scores, letters of recommendation and prior research experience. Both the IGP and METP have been very successful in promoting minority student admissions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007563-20
Application #
7231411
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
1998-07-01
Project End
2008-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
20
Fiscal Year
2007
Total Cost
$581,899
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Physiology
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Gibbons, Hunter R; Shaginurova, Guzel; Kim, Laura C et al. (2018) Divergent lncRNA GATA3-AS1 Regulates GATA3 Transcription in T-Helper 2 Cells. Front Immunol 9:2512
Zhu, Lin; Shi, Jeanne; Luu, Thao N et al. (2018) Hepatocyte estrogen receptor alpha mediates estrogen action to promote reverse cholesterol transport during Western-type diet feeding. Mol Metab 8:106-116
Marks, Christian R; Shonesy, Brian C; Wang, Xiaohan et al. (2018) Activated CaMKII? Binds to the mGlu5 Metabotropic Glutamate Receptor and Modulates Calcium Mobilization. Mol Pharmacol 94:1352-1362
Williams, Ian M; Valenzuela, Francisco A; Kahl, Steven D et al. (2018) Insulin exits skeletal muscle capillaries by fluid-phase transport. J Clin Invest 128:699-714
Vierra, Nicholas C; Dickerson, Matthew T; Philipson, Louis H et al. (2018) Simultaneous Real-Time Measurement of the ?-Cell Membrane Potential and Ca2+ Influx to Assess the Role of Potassium Channels on ?-Cell Function. Methods Mol Biol 1684:73-84
McDonnell, Wyatt J; Koethe, John R; Mallal, Simon A et al. (2018) High CD8 T-Cell Receptor Clonality and Altered CDR3 Properties Are Associated With Elevated Isolevuglandins in Adipose Tissue During Diet-Induced Obesity. Diabetes 67:2361-2376
Vierra, Nicholas C; Dickerson, Matthew T; Jordan, Kelli L et al. (2018) TALK-1 reduces delta-cell endoplasmic reticulum and cytoplasmic calcium levels limiting somatostatin secretion. Mol Metab 9:84-97
Rossi, Mario; Zhu, Lu; McMillin, Sara M et al. (2018) Hepatic Gi signaling regulates whole-body glucose homeostasis. J Clin Invest 128:746-759
Syring, Kristen E; Bosma, Karin J; Oeser, James K et al. (2018) The Diabetes Susceptibility Gene SLC30A8 that Encodes the Zinc Transporter ZnT8 is a Pseudogene in Guinea Pigs Potentially Contributing to Low Guinea Pig Islet Zinc Content. J Mol Evol 86:613-617
Cottam, Matthew A; Itani, Hana A; Beasley 4th, Arch A et al. (2018) Links between Immunologic Memory and Metabolic Cycling. J Immunol 200:3681-3689

Showing the most recent 10 out of 217 publications