Burnham Hope V, Cizauskas Hannah E, Barefield David Y
Department of Cell and Molecular Physiology, Loyola University Chicago, Maywood, Illinois, United States.
Am J Physiol Heart Circ Physiol. 2024 Mar 1;326(3):H568-H583. doi: 10.1152/ajpheart.00252.2023. Epub 2023 Dec 29.
The molecular mechanisms of sarcomere proteins underlie the contractile function of the heart. Although our understanding of the sarcomere has grown tremendously, the focus has been on ventricular sarcomere isoforms due to the critical role of the ventricle in health and disease. However, atrial-specific or -enriched myofilament protein isoforms, as well as isoforms that become expressed in disease, provide insight into ways this complex molecular machine is fine-tuned. Here, we explore how atrial-enriched sarcomere protein composition modulates contractile function to fulfill the physiological requirements of atrial function. We review how atrial dysfunction negatively affects the ventricle and the many cardiovascular diseases that have atrial dysfunction as a comorbidity. We also cover the pathophysiology of mutations in atrial-enriched contractile proteins and how they can cause primary atrial myopathies. Finally, we explore what is known about contractile function in various forms of atrial fibrillation. The differences in atrial function in health and disease underscore the importance of better studying atrial contractility, especially as therapeutics currently in development to modulate cardiac contractility may have different effects on atrial sarcomere function.
肌节蛋白的分子机制是心脏收缩功能的基础。尽管我们对肌节的理解有了极大的增长,但由于心室在健康和疾病中的关键作用,研究重点一直放在心室肌节亚型上。然而,心房特异性或富集的肌丝蛋白亚型,以及在疾病中表达的亚型,为了解这一复杂分子机器如何进行微调提供了线索。在这里,我们探讨富含心房的肌节蛋白组成如何调节收缩功能,以满足心房功能的生理需求。我们回顾了心房功能障碍如何对心室产生负面影响,以及许多以心房功能障碍为合并症的心血管疾病。我们还阐述了富含心房的收缩蛋白突变的病理生理学,以及它们如何导致原发性心房肌病。最后,我们探讨了目前已知的各种形式心房颤动中的收缩功能。健康和疾病状态下心房功能的差异凸显了更好地研究心房收缩性的重要性,特别是因为目前正在开发的调节心脏收缩性的疗法可能对心房肌节功能有不同影响。