Myocardial ischemia negatively impacts cardiac function through: 1) Immediate post-ischemic contractile dysfunction of non-infarcted, reperfused myocardium (stunning); 2) Myocardial infarction and infarct extension; and 3) Delayed left ventricular remodeling. Since cardiac ischemia and infarction are associated with increased free cytosolic calcium, activation of calpains (calcium-activated cystein proteases) is thought to contribute to ischemic cardiac injury. Limb-Girdle Muscular Dystrophy 2A (or """"""""calpainopathy"""""""") in patients with loss of function mutations in the calpain-3 gene result reveals an essential function for calpains in skeletal muscle health. We have created a myocardial calpain loss-of-function mouse (transgenic overexpression of calpain-inhibitory calpastatin) which develops a cardiomyopathy with many of the histologic features of skeletal calpainopathy. Based on these observations, our GENERAL HYPOTHESIS is that calpains 1 and 2 have unique functions in normal cardiac health, and due to differential activation by calcium and differential mRNA regulation after infarction, play distinct roles in mediating post-ischemic injury. To test this hypothesis we created cardiac-specific calpain 1 and 2 knockout and conditional overexpression mice, and will pursue these SPECIFIC AIMS: SA #1 -Define the normal functions of myocardial calpain 1 and calpain 2 in studies of cardiac structure, function, and cell signaling. SA#2-Delineate the pathophysiological consequences and relevant cellular mechanisms of calpain 1 and calpain 2 activation after myocardial infarction and ischemia-reperfusion injury by defining the relative roles of apoptotic and necrotic cardiomyocyte death. SA#3-Determine the biochemical mechanisms for calpain-mediated caspase activation and stimulation of apoptosis in studies of calpain 1 and 2-modulated cultured neonatal and adult cardiac myocytes. Collectively, these studies will apply state-of-the-art techniques for in vivo genetic manipulation, microphysiologic analysis, and biochemical assessment to achieve insight into the roles of myocardial calpains in health and disease. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
7R01HL080008-03
Application #
7554388
Study Section
Myocardial Ischemia and Metabolism Study Section (MIM)
Program Officer
Adhikari, Bishow B
Project Start
2006-08-01
Project End
2011-07-31
Budget Start
2008-03-01
Budget End
2008-07-31
Support Year
3
Fiscal Year
2007
Total Cost
$161,679
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Matkovich, Scot J; Van Booven, Derek J; Eschenbacher, William H et al. (2011) RISC RNA sequencing for context-specific identification of in vivo microRNA targets. Circ Res 108:18-26
Dorn 2nd, Gerald W (2011) Nix Nought Nothing: fairy tale or real deal. J Mol Cell Cardiol 51:497-500
Zhang, Yan; Matkovich, Scot J; Duan, Xiujun et al. (2011) Receptor-independent protein kinase C alpha (PKCalpha) signaling by calpain-generated free catalytic domains induces HDAC5 nuclear export and regulates cardiac transcription. J Biol Chem 286:26943-51
Dorn 2nd, Gerald W (2011) MicroRNAs in cardiac disease. Transl Res 157:226-35
Eijkelkamp, Niels; Heijnen, Cobi J; Willemen, Hanneke L D M et al. (2010) GRK2: a novel cell-specific regulator of severity and duration of inflammatory pain. J Neurosci 30:2138-49
Dorn 2nd, Gerald W (2010) MicroRNAs: redefining mechanisms in cardiac disease. J Cardiovasc Pharmacol 56:589-95
Nijboer, Cora H; Heijnen, Cobi J; Willemen, Hanneke L D M et al. (2010) Cell-specific roles of GRK2 in onset and severity of hypoxic-ischemic brain damage in neonatal mice. Brain Behav Immun 24:420-6
Kang, Min-Young; Zhang, Yan; Matkovich, Scot J et al. (2010) Receptor-independent cardiac protein kinase Calpha activation by calpain-mediated truncation of regulatory domains. Circ Res 107:903-12
Cappola, Thomas P; Li, Mingyao; He, Jing et al. (2010) Common variants in HSPB7 and FRMD4B associated with advanced heart failure. Circ Cardiovasc Genet 3:147-54
Matkovich, Scot J; Van Booven, Derek J; Cappola, Thomas P et al. (2010) Association of an intronic, but not any exonic, FRMD4B sequence variant and heart failure. Clin Transl Sci 3:134-9

Showing the most recent 10 out of 25 publications