This review highlights how mechanical forces on cardiac myocytes are transduced into chemical signals via ROS and NO pathways to regulate calcium handling, providing insights into the Frank-Starling law, the Anrep effect, and arrhythmogenesis.
Abstract The heart has the ability to adjust to changing mechanical loads. The Frank–Starling law and the Anrep effect describe exquisite intrinsic mechanisms the heart has for autoregulating the force of contraction to maintain cardiac output under changes of preload and afterload. Although these mechanisms have been known for more than a century, their cellular and molecular underpinnings are still debated. How does the cardiac myocyte sense changes in preload or afterload? How does the myocyte adjust its response to compensate for such changes? In cardiac myocytes Ca 2+ is a crucial regulator of contractile force and in this review we compare and contrast recent studies from different labs that address these two important questions. The ‘dimensionality’ of the mechanical milieu under which experiments are carried out provide important clues to the location of the mechanosensors and the kinds of mechanical forces they can sense and respond to. As a first approximation, sensors inside the myocyte appear to modulate reactive oxygen species while sensors on the cell surface appear to also modulate nitric oxide signalling; both signalling pathways affect Ca 2+ handling. Undoubtedly, further studies will add layers to this simplified picture. Clarifying the intimate links from cellular mechanics to reactive oxygen species and nitric oxide signalling and to Ca 2+ handling will deepen our understanding of the Frank–Starling law and the Anrep effect, and also provide a unified view on how arrhythmias may arise in seemingly disparate diseases that have in common altered myocyte mechanics. image
Chen‐Izu et al. (Fri,) studied this question.