The goal of this application is to support the development of Dr. Peter M. Snyder as a clinician scientist so that at the completion of the award he will be an independent researcher and an outstanding academic scientist and clinician. Dr. Michael J. Welsh will assume responsibility as mentor to ensure the success of the development plan. The heart of the proposal is an intensive training experience in the basic research laboratory. Dr. Snyder will study the epithelial Na+ channel, ENAC. Mutations in the Beta and gammaENaC subunits of ENaC cause Liddle's syndrome, an inherited form of hypertension. Dr. Snyder's preliminary studies indicate that Liddle's mutations increase Na+ current through ENaC. The three major aims of his research proposal are to understand how Liddle's-associated mutations increase ENaC Na+ current, how ENaC is regulated, and how the ENaC subunits contribute to the formation of a Na+ channel pore. These basic studies will provide him with training required to develop skills in molecular biology, cell biology, and patch-clamp electrophysiology. In addition, he will further develop his skills at using the scientific method to develop hypotheses that can be experimentally tested to yield unequivocal answers. In addition to basic research training Dr. Snyder will continue his training in biologic science with didactic courses, seminars and journal clubs. He will receive instruction in speaking and writing and will receive instruction in the responsible conduct of research. He will also attend national meetings to present his own work and to learn from others. Both the mentor and the institution are highly committed to the applicant's scientific development and academic success.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HL003575-03
Application #
2750278
Study Section
Special Emphasis Panel (ZHL1-CSR-Y (M1))
Project Start
1996-09-05
Project End
2001-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Snyder, Peter M; Steines, Jennifer C; Olson, Diane R (2004) Relative contribution of Nedd4 and Nedd4-2 to ENaC regulation in epithelia determined by RNA interference. J Biol Chem 279:5042-6
Snyder, Peter M; Olson, Diane R; Thomas, Brittany C (2002) Serum and glucocorticoid-regulated kinase modulates Nedd4-2-mediated inhibition of the epithelial Na+ channel. J Biol Chem 277:5-8
Snyder, Peter M (2002) The epithelial Na+ channel: cell surface insertion and retrieval in Na+ homeostasis and hypertension. Endocr Rev 23:258-75
McDonald, Fiona J; Western, Andrea H; McNeil, John D et al. (2002) Ubiquitin-protein ligase WWP2 binds to and downregulates the epithelial Na(+) channel. Am J Physiol Renal Physiol 283:F431-6
Snyder, P M; Olson, D R; McDonald, F J et al. (2001) Multiple WW domains, but not the C2 domain, are required for inhibition of the epithelial Na+ channel by human Nedd4. J Biol Chem 276:28321-6
Askwith, C C; Benson, C J; Welsh, M J et al. (2001) DEG/ENaC ion channels involved in sensory transduction are modulated by cold temperature. Proc Natl Acad Sci U S A 98:6459-63
Snyder, P M; Bucher, D B; Olson, D R (2000) Gating induces a conformational change in the outer vestibule of ENaC. J Gen Physiol 116:781-90
Snyder, P M (2000) Liddle's syndrome mutations disrupt cAMP-mediated translocation of the epithelial Na(+) channel to the cell surface. J Clin Invest 105:45-53
Ambrosius, W T; Bloem, L J; Zhou, L et al. (1999) Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension. Hypertension 34:631-7
Adams, C M; Snyder, P M; Welsh, M J (1997) Interactions between subunits of the human epithelial sodium channel. J Biol Chem 272:27295-300