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Am J Physiol Cell Physiol (October 24, 2007). doi:10.1152/ajpcell.00146.2007
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Submitted on April 7, 2007
Accepted on October 19, 2007

Co-expression of skeletal and cardiac troponin T decreases mouse cardiac function

Qi-Quan Huang1, Hanzhong Feng2, Jing Liu3, Jianfeng Du3, Linda B. Stull4, Christine Moravec5, Xupei Huang6, and J.-P. Jin7*

1 Medicine, Northwestern University, Chicago, Illinois, United States
2 Medicine, Northwestern University, Evanston, Illinois, United States; Evanston, Illinois, United States
3 Biological Sciences, Florida Atlantic University, Boca Raton, Florida, United States
4 Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland, Illinois, United States
5 Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland, Ohio, United States
6 Biomedical Science, Florida Atlantic University, Boca Raton, Florida, United States
7 Medicine, Northwestern University, Evanston, Illinois, United States

* To whom correspondence should be addressed. E-mail: jpjin{at}northwestern.edu.

In contrast to skeletal muscles that simultaneously express multiple troponin T (TnT) isoforms, normal adult human cardiac muscle contains a single isoform of cardiac TnT. To understand the significance of myocardial TnT homogeneity, we examined the effect of TnT heterogeneity on heart function. Transgenic mouse hearts over-expressing a fast skeletal muscle TnT together with the endogenous cardiac TnT was investigated in vivo and ex vivo as an experimental system of concurrent presence of two classes of TnT in the adult cardiac muscle. This model of myocardial TnT heterogeneity produced pathogenic phenotypes: Echocardiograph imaging detected age-progressive reductions of cardiac function; in vivo left ventricular pressure analysis showed decreased myocardial contractility; ex vivo analysis of isolated working heart preparations confirmed an intrinsic decrease of cardiac function in the absence of neurohumoral influence. The transgenic mice also showed chronic myocardial hypertrophy and degeneration. The dominantly negative effects of introducing a fast TnT into the cardiac thin filaments to produce two classes of Ca2+ regulatory units in the adult myocardium suggest that TnT heterogeneity decreases contractile function by disrupting the synchronized action during ventricular contraction that is normally activated as an electrophysiological syncytium.




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