Conditional expression of a G i -coupled receptor causes ventricular conduction delay and a lethal cardiomyopathy

Cardiomyopathy is a major cause of morbidity and mortality. Ventricular conduction delay, as shown by prolonged deflections in the electrocardiogram caused by delayed ventricular contraction (wide QRS complex), is a common feature of cardiomyopathy and is associated with a poor prognosis. Although t...

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Published in:	Proceedings of the National Academy of Sciences - PNAS Vol. 97; no. 9; pp. 4826 - 4831
Main Authors:	Redfern, Charles H., Degtyarev, Michael Y., Kwa, Andrew T., Salomonis, Nathan, Cotte, Nathalie, Nanevicz, Tania, Fidelman, Nick, Desai, Kavin, Vranizan, Karen, Lee, Elena K., Coward, Peter, Shah, Nila, Warrington, Janet A., Fishman, Glenn I., Bernstein, Daniel, Baker, Anthony J., Conklin, Bruce R.
Format:	Journal Article
Language:	English
Published:	25-04-2000
Online Access:	Get full text
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Summary:	Cardiomyopathy is a major cause of morbidity and mortality. Ventricular conduction delay, as shown by prolonged deflections in the electrocardiogram caused by delayed ventricular contraction (wide QRS complex), is a common feature of cardiomyopathy and is associated with a poor prognosis. Although the G i -signaling pathway is up-regulated in certain cardiomyopathies, previous studies suggested this up-regulation was compensatory rather than a potential cause of the disease. Using the tetracycline transactivator system and a modified G i -coupled receptor (Ro1), we provide evidence that increased G i signaling in mice can result in a lethal cardiomyopathy associated with a wide QRS complex arrhythmia. Induced expression of Ro1 in adult mice resulted in a >90% mortality rate at 16 wk, whereas suppression of Ro1 expression after 8 wk protected mice from further mortality and allowed partial improvement in systolic function. Results of DNA-array analysis of over 6,000 genes from hearts expressing Ro1 are consistent with hyperactive G i signaling. DNA-array analysis also identified known markers of cardiomyopathy and hundreds of previously unknown potential diagnostic markers and therapeutic targets for this syndrome. Our system allows cardiomyopathy to be induced and reversed in adult mice, providing an unprecedented opportunity to dissect the role of G i signaling in causing cardiac pathology.
ISSN:	0027-8424 1091-6490
DOI:	10.1073/pnas.97.9.4826