This project seeks to examine specific excitation-contraction coupling mechanisms in bladder smooth muscle cells, and to determine whether these processes are associated with the contractile dysfunction known to occur with chronic obstruction of the urinary bladder. Particular focus will be on the molecular mechanisms underlying calcium-induced calcium release (CICR) in bladder smooth muscle cells, using laser scanning confocal microscopy and patch clamp methods. Calcium-induced calcium release, or the release of intracellular calcium ions by the influx of calcium across the cell membrane, has been shown to play an important role in excitation-contraction coupling in bladder myocytes. Evidence suggests that impairment of this process is associated with the adaptive changes that occur in bladder smooth muscle during outlet obstruction. We will determine the biophysical characteristics of CICR in normal urinary bladder myocytes and compare that with observations in myocytes from obstructed bladders. Knockout mice with targeted deletions of ryanodine receptors will be generated and the CICR process examined to determine the role of specific intracellular calcium channels and associated modulatory proteins in excitation-contraction coupling of bladder smooth muscle.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK058795-04
Application #
6700009
Study Section
Special Emphasis Panel (ZRG1-UROL (01))
Program Officer
Mullins, Christopher V
Project Start
2001-03-01
Project End
2005-01-31
Budget Start
2004-02-01
Budget End
2005-01-31
Support Year
4
Fiscal Year
2004
Total Cost
$261,489
Indirect Cost
Name
Cornell University
Department
Other Basic Sciences
Type
Schools of Veterinary Medicine
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Ledoux, Jonathan; Taylor, Mark S; Bonev, Adrian D et al. (2008) Functional architecture of inositol 1,4,5-trisphosphate signaling in restricted spaces of myoendothelial projections. Proc Natl Acad Sci U S A 105:9627-32
Kotlikoff, Michael I (2007) Genetically encoded Ca2+ indicators: using genetics and molecular design to understand complex physiology. J Physiol 578:55-67
Tallini, Yvonne N; Ohkura, Masamichi; Choi, Bum-Rak et al. (2006) Imaging cellular signals in the heart in vivo: Cardiac expression of the high-signal Ca2+ indicator GCaMP2. Proc Natl Acad Sci U S A 103:4753-8
Ji, Guangju; Feldman, Morris E; Greene, Kai Su et al. (2004) RYR2 proteins contribute to the formation of Ca(2+) sparks in smooth muscle. J Gen Physiol 123:377-86
Kotlikoff, Michael I; Kannan, Mathur S; Solway, Julian et al. (2004) Methodologic advancements in the study of airway smooth muscle. J Allergy Clin Immunol 114:S18-31
Elble, Randolph C; Ji, Guangju; Nehrke, Keith et al. (2002) Molecular and functional characterization of a murine calcium-activated chloride channel expressed in smooth muscle. J Biol Chem 277:18586-91
Xin, H-B; Deng, K-Y; Rishniw, M et al. (2002) Smooth muscle expression of Cre recombinase and eGFP in transgenic mice. Physiol Genomics 10:211-5
Ji, Guangju; Barsotti, Robert J; Feldman, Morris E et al. (2002) Stretch-induced calcium release in smooth muscle. J Gen Physiol 119:533-44