Document Detail


Cytoskeletal networks and the regulation of cardiac contractility: microtubules, hypertrophy, and cardiac dysfunction.
MedLine Citation:
PMID:  16679401     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The cytoskeleton as classically defined for eukaryotic cells consists of three systems of protein filaments: the microtubules, the intermediate filaments, and the microfilaments. In mature striated muscle such as the heart of the adult mammal, these three types of cytoskeletal filaments are superimposed spatially on the myofilaments, a specialized system of contractile protein filaments. Each of these systems of protein filaments has the potential to respond in an adaptive or maladaptive manner during load-induced hypertrophic cardiac growth. However, the extent to which such hypertrophy is compensatory is also critically dependent on the type of hemodynamic overload that serves as the hypertrophic stimulus. Thus cardiac hypertrophy is not intrinsically maladaptive; rather, it is the nature of the inducing load rather than hypertrophy itself that is responsible, through effects on structural and/or regulatory proteins, for the frequent deterioration of initially compensatory hypertrophy into the congestive heart failure state. As one example reviewed here of this load specificity of maladaptation, increased microtubule network density is a persistent feature of severely pressure-overloaded, hypertrophied, and failing myocardium that imposes a primarily viscous load on active myofilaments during contraction.
Authors:
George Cooper
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review     Date:  2006-05-05
Journal Detail:
Title:  American journal of physiology. Heart and circulatory physiology     Volume:  291     ISSN:  0363-6135     ISO Abbreviation:  Am. J. Physiol. Heart Circ. Physiol.     Publication Date:  2006 Sep 
Date Detail:
Created Date:  2006-08-10     Completed Date:  2006-09-26     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  100901228     Medline TA:  Am J Physiol Heart Circ Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  H1003-14     Citation Subset:  IM    
Affiliation:
Gazes Cardiac Research Institute, Cardiology Division, PO Box 250773, Medical University of South Carolina, and Department of Veterans Affairs Medical Center, Charleston, SC 29403, USA. cooperge@musc.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Biomechanics
Cytoskeleton / physiology*,  ultrastructure
Heart / physiopathology*
Heart Diseases / physiopathology
Humans
Hypertrophy
Microfilaments / physiology,  ultrastructure
Microtubules / physiology*,  ultrastructure
Myocardial Contraction / physiology*
Myocardium / pathology*
Grant Support
ID/Acronym/Agency:
HL-48788/HL/NHLBI NIH HHS

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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