Atomic force microscopy (AFM) is a valuable tool for assessing biomechanics in arrhythmogenic cardiomyopathy, revealing abnormalities in cytoskeleton, cell membrane structures, and contractility.
Atomic force microscopy provides unique insights into the cellular mechanobiology and biomechanical defects underlying arrhythmogenic cardiomyopathy.
Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disorder characterized by progressive replacement of cardiomyocytes by fibrofatty tissue, ventricular dilatation, cardiac dysfunction, arrhythmias, and sudden cardiac death. Interest in molecular biomechanics for these disorders is constantly growing. Atomic force microscopy (AFM) is a well-established technic to study the mechanobiology of biological samples under physiological and pathological conditions at the cellular scale. However, a review which described all the different data that can be obtained using the AFM (cell elasticity, adhesion behavior, viscoelasticity, beating force, and frequency) is still missing. In this review, we will discuss several techniques that highlight the potential of AFM to be used as a tool for assessing the biomechanics involved in ACM. Indeed, analysis of genetically mutated cells with AFM reveal abnormalities of the cytoskeleton, cell membrane structures, and defects of contractility. The higher the Young's modulus, the stiffer the cell, and it is well known that abnormal tissue stiffness is symptomatic of a range of diseases. The cell beating force and frequency provide information during the depolarization and repolarization phases, complementary to cell electrophysiology (calcium imaging, MEA, patch clamp). In addition, original data is also presented to emphasize the unique potential of AFM as a tool to assess fibrosis in cardiac tissue.
Peña et al. (Mon,) conducted a review in Arrhythmogenic cardiomyopathy (ACM). Atomic force microscopy (AFM) was evaluated. Atomic force microscopy (AFM) is a valuable tool for assessing biomechanics in arrhythmogenic cardiomyopathy, revealing abnormalities in cytoskeleton, cell membrane structures, and contractility.