Abstract |
Familial hypertrophic cardiomyopathy (FHC) is a disease caused by mutations in contractile proteins of the sarcomere. Our laboratory developed a mouse model of FHC with a mutation in the thin filament protein alpha-tropomyosin (TM) at amino acid 180 (Glu180Gly). The hearts of these mice exhibit dramatic systolic and diastolic dysfunction, and their myofilaments demonstrate increased calcium sensitivity. The mice also develop severe cardiac hypertrophy, with death ensuing by 6 mo. In an attempt to normalize calcium sensitivity in the cardiomyofilaments of the hypertrophic mice, we generated a chimeric alpha-/beta-TM protein that decreases calcium sensitivity in transgenic mouse cardiac myofilaments. By mating mice from these two models together, we tested the hypothesis that an attenuation of myofilament calcium sensitivity would modulate the severe physiological and pathological consequences of the FHC mutation. These double-transgenic mice "rescue" the hypertrophic phenotype by exhibiting a normal morphology with no pathological abnormalities. Physiological analyses of these rescued mice show improved cardiac function and normal myofilament calcium sensitivity. These results demonstrate that alterations in calcium response by modification of contractile proteins can prevent the pathological and physiological effects of this disease.
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Authors | Ganapathy Jagatheesan, Sudarsan Rajan, Natalia Petrashevskaya, Arnold Schwartz, Greg Boivin, Grace M Arteaga, R John Solaro, Stephen B Liggett, David F Wieczorek |
Journal | American journal of physiology. Heart and circulatory physiology
(Am J Physiol Heart Circ Physiol)
Vol. 293
Issue 2
Pg. H949-58
(Aug 2007)
ISSN: 0363-6135 [Print] United States |
PMID | 17416600
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Adrenergic beta-Agonists
- RNA, Messenger
- Recombinant Fusion Proteins
- Tpm1 protein, mouse
- Tropomyosin
- Isoproterenol
- Calcium
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Topics |
- Actin Cytoskeleton
(drug effects, metabolism)
- Adrenergic beta-Agonists
(pharmacology)
- Animals
- Calcium
(metabolism)
- Cardiomyopathy, Hypertrophic, Familial
(genetics, metabolism, pathology, physiopathology, therapy)
- Disease Models, Animal
- Dose-Response Relationship, Drug
- Gene Transfer Techniques
- Genetic Therapy
(methods)
- Genotype
- Heart Rate
- Isoproterenol
(pharmacology)
- Mice
- Mice, Transgenic
- Mutation
- Myocardial Contraction
(drug effects)
- Myocardium
(metabolism, pathology)
- Phenotype
- RNA, Messenger
(metabolism)
- Recombinant Fusion Proteins
(metabolism)
- Sarcomeres
(metabolism)
- Severity of Illness Index
- Time Factors
- Tropomyosin
(genetics, metabolism)
- Ventricular Pressure
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