This is a renewal of a research training program which is now in its 10th year. The purpose of this program is to training promising young scientists for research careers in molecular excitability of the cardiovascular system. The emphasis of the grant is ion channels, the fundamental units of cardiac excitability. Ion channels, in concert with ion pumps and transporters, generate a coordinated responses of the whole heart. A higher degree of control of cardiovascular function is provided by the nervous system. Both the central and the peripheral (autonomic) nervous systems control and coordinate cardiovascular homeostasis. The sympathetic and the parasympathetic branches of the autonomic nervous system release norepinephrine and acetylcholine, respectively, to control impulse coordination and contractility in the heart. Interaction of neurotransmitters with cell surface receptors trigger a cascade of intracellular events. Our program covers several topics that are important to cardiac function: K+ channels, Ca/2+ channels, transporters, regulation of intracellular Ca/2+, neuronal regulation of cardiac function, beta-adrenergic receptors, intracellular signaling pathways, drug delivery, and the molecular basis of human cardiac diseases. The experimental approaches include electrophysiology, fluorescence imaging, molecular biology, protein biochemistry, spectroscopy, NMR, x-ray crystallography, and cryoelectron microscopy/angular reconstitution. The training program is designed for 4 predoctoral and 6 postdoctoral trainees (1 zero year, one first year, 2 second year, 2 third year). Predoctoral training is 4 to 5 years duration while postdoctoral training is for 2-3 years. In addition to the research opportunities in the laboratories of the training faculty, the program offers trainees other enrichment activities including a yearly detrimental symposium, a core laboratory for """"""""hands-on"""""""" training in electrophysiology, fluorescence imaging, and production of transgenic and knockout animals, grant critique sessions, panel discussions and journal clubs.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL007676-14
Application #
6536689
Study Section
Special Emphasis Panel (ZHL1-CSR-K (F1))
Program Officer
Commarato, Michael
Project Start
1994-07-01
Project End
2004-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
14
Fiscal Year
2002
Total Cost
$141,453
Indirect Cost
Name
Baylor College of Medicine
Department
Physiology
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Tanner, Mark R; Pennington, Michael W; Chamberlain, Brayden H et al. (2018) Targeting KCa1.1 Channels with a Scorpion Venom Peptide for the Therapy of Rat Models of Rheumatoid Arthritis. J Pharmacol Exp Ther 365:227-236
Loehr, James Anthony; Wang, Shang; Cully, Tanya R et al. (2018) NADPH oxidase mediates microtubule alterations and diaphragm dysfunction in dystrophic mice. Elife 7:
Jarrett, Kelsey E; Lee, Ciaran; De Giorgi, Marco et al. (2018) Somatic Editing of Ldlr With Adeno-Associated Viral-CRISPR Is an Efficient Tool for Atherosclerosis Research. Arterioscler Thromb Vasc Biol 38:1997-2006
Nikolaev, Sergey I; Vetiska, Sandra; Bonilla, Ximena et al. (2018) Somatic Activating KRAS Mutations in Arteriovenous Malformations of the Brain. N Engl J Med 378:250-261
Herman, Alexander M; Rhyner, Alexander M; Devine, W Patrick et al. (2018) A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse. Biol Open 7:
Fish, Jason E; Cantu Gutierrez, Manuel; Dang, Lan T et al. (2017) Dynamic regulation of VEGF-inducible genes by an ERK/ERG/p300 transcriptional network. Development 144:2428-2444
Ren, Pingping; Hughes, Michael; Krishnamoorthy, Swapna et al. (2017) Critical Role of ADAMTS-4 in the Development of Sporadic Aortic Aneurysm and Dissection in Mice. Sci Rep 7:12351
Brinegar, Amy E; Xia, Zheng; Loehr, James Anthony et al. (2017) Extensive alternative splicing transitions during postnatal skeletal muscle development are required for calcium handling functions. Elife 6:
Quick, Ann P; Landstrom, Andrew P; Wang, Qiongling et al. (2017) Novel junctophilin-2 mutation A405S is associated with basal septal hypertrophy and diastolic dysfunction. JACC Basic Transl Sci 2:56-67
Jarrett, Kelsey E; Lee, Ciaran M; Yeh, Yi-Hsien et al. (2017) Somatic genome editing with CRISPR/Cas9 generates and corrects a metabolic disease. Sci Rep 7:44624

Showing the most recent 10 out of 102 publications