Micro- and nanoscale biophysical cues for cardiovascular disease therapy

After cardiovascular injury, numerous pathological processes adversely impact the homeostatic function of cardiomyocyte, macrophage, fibroblast, endothelial cell, and vascular smooth muscle cell populations. Subsequent malfunctioning of these cells may further contribute to cardiovascular disease onset and progression. By modulating cellular responses after injury, it is possible to create local environments that promote wound healing and tissue repair mechanisms. The extracellular matrix continuously provides these mechanosensitive cell types with physical cues spanning the micro- and nanoscale to influence behaviors such as adhesion, morphology, and phenotype. It is therefore becoming increasingly compelling to harness these cell–substrate interactions to elicit more native cell behaviors that impede cardiovascular disease progression and enhance regenerative potential. This review discusses recent in vitro and preclinical work that have demonstrated the therapeutic implications of micro- and nanoscale biophysical cues on cell types adversely affected in cardiovascular diseases — cardiomyocytes, macrophages, fibroblasts, endothelial cells, and vascular smooth muscle cells. Micro- and nanoscale topographies that mimic biophysical cues observed in native tissue architectures can be used to modulate pathological behaviors of adversely impacted cell types involved in cardiovascular diseases – cardiomyocytes, macrophages, fibroblasts, endothelial cells, and vascular smooth muscle cells – to promote wound healing and tissue repair mechanisms. [Display omitted]