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Published on: June 14, 2016
Inflammatory cardiomyopathy: there is a specific matrix destruction in the course of the disease
1Baylor College of Medicine, Texas Children's Hospital, Houston 77030, USA. jtowbin@bcm.tmc.edu
Insights
Dilated cardiomyopathy (DCM) involves cytoskeleton and sarcolemma disruption, impacting heart function and leading to heart failure. Dystrophin mutations and impaired stretch sensing are key factors in DCM progression.
Area of Science:
- Cardiology
- Molecular Biology
- Pathology
Background:
- Cardiomyopathies contribute significantly to heart failure, sudden death, and transplantation needs.
- Understanding the molecular mechanisms underlying these disorders is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the hypothesis that dilated cardiomyopathy (DCM) originates from cytoskeleton/sarcolemma defects affecting sarcomere function.
- To explore the role of dystrophin and stretch-sensing complexes in DCM pathogenesis.
Main Methods:
- Evaluation of sarcolemma and extracellular matrix (ECM) in DCM and systolic heart failure.
- Analysis of dystrophin interactions with ECM, sarcomere, and nucleus.
- Assessment of the T-cap/MLP/alpha-actinin/titin complex in Z-disc stabilization and mechanical stretch sensing.
Main Results:
- Sarcolemma membrane disruption and secondary ECM architectural changes observed in DCM.
- Disruption of dystrophin-mediated links may cause a domino effect on systolic function and arrhythmias.
- Defective stretch sensing in myocytes leads to cell death pathways and heart failure progression.
Conclusions:
- DCM may stem from cytoskeleton/sarcolemma disruption, with dystrophin mutations implicated in idiopathic DCM.
- Impaired mechanical stretch sensing by the T-cap/MLP/alpha-actinin/titin complex contributes to myocyte dysfunction and heart failure.
- Viral myocarditis shares clinical and mechanistic similarities with genetic DCM, suggesting common pathways.
Abstract:
Cardiomyopathies are responsible for a high proportion of cases of congestive heart failure and sudden death, as well as for the need for transplantation. Understanding of the causes of these disorders has been sought in earnest over the past decade. We hypothesized that DCM is a disease of the cytoskeleton/sarcolemma, which affects the sarcomere. Evaluation of the sarcolemma in DCM and other forms of systolic heart failure demonstrates membrane disruption; and, secondarily, the extracellular matrix architecture is also affected. Disruption of the links from the sarcolemma to ECM at the dystrophin C-terminus and those to the sarcomere and nucleus via N-terminal dystrophin interactions could lead to a "domino effect" disruption of systolic function and development of arrhythmias. We also have suggested that dystrophin mutations play a role in idiopathic DCM in males. The T-cap/MLP/alpha-actinin/titin complex appears to stabilize Z-disc function via mechanical stretch sensing. Loss of elasticity results in the primary defect in the endogenous cardiac muscle stretch sensor machinery. The over-stretching of individual myocytes leads to activation of cell death pathways, at a time when stretch-regulated survival cues are diminished due to defective stretch sensing, leading to progression of heart failure. Genetic DCM and the acquired disorder viral myocarditis have the same clinical features including heart failure, arrhythmias, and conduction block, and also similar mechanisms of disease based on the proteins targeted. In dilated cardiomyopathy, the process of progressive ventricular dilation and changes of the shape of the ventricle to a more spherical shape, associated with changes in ventricular function and/or hypertrophy, occurs without known initiating disturbance. In those cases in which resolution of cardiac dysfunction does not occur, chronic DCM results. It has been unclear what the underlying etiology of this long-term sequela could be, but viral persistence and autoimmunity have been widely speculated.
Related Concept Videos
Myocarditis I: Introduction
Cardiomyopathy I: Introduction and Classification
Myocarditis II: Clinical Features and Diagnostic Tests
Cardiomyopathy II: Dilated Cardiomyopathy
Rheumatic Heart Disease I: Introduction
Cardiomyopathy IV: Restrictive Cardiomyopathy
