| Literature DB >> 31886450 |
Yasser Aboelkassem1, Joseph D Powers1, Kimberly J McCabe2, Andrew D McCulloch1.
Abstract
Myocardial hypertrophy is the result of sustained perturbations to the mechanical and/or neurohormonal homeostasis of cardiac cells and is driven by integrated, multiscale biophysical and biochemical processes that are currently not well defined. In this brief review, we highlight recent computational and experimental models of cardiac hypertrophy that span mechanisms from the molecular level to the tissue level. Specifically, we focus on: (i) molecular-level models of the structural dynamics of sarcomere proteins in hypertrophic hearts, (ii) cellular-level models of excitation-contraction coupling and mechanosensitive signaling in disease-state myocytes, and (iii) organ-level models of myocardial growth kinematics and predictors thereof. Finally, we discuss how spanning these scales and combining multiple experimental/computational models will provide new information about the processes governing hypertrophy and potential methods to prevent or reverse them.Entities:
Keywords: Cardiac Myofilament; Hypertrophic Cardiomyopathy; Multiscale Modeling; Sarcomeric Point Mutations
Year: 2019 PMID: 31886450 PMCID: PMC6934086 DOI: 10.1016/j.cobme.2019.09.005
Source DB: PubMed Journal: Curr Opin Biomed Eng ISSN: 2468-4511