Department of Physiology, Pennsylvania Muscle Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Penn Cardiovascular Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Exp Biol Med (Maywood). 2019 Nov;244(15):1255-1272. doi: 10.1177/1535370219868960. Epub 2019 Aug 9.
Cardiomyocytes are large (∼40,000 µm), rod-shaped muscle cells that provide the working force behind each heartbeat. These highly structured cells are packed with dense cytoskeletal networks that can be divided into two groups—the contractile (i.e. sarcomeric) cytoskeleton that consists of filamentous actin-myosin arrays organized into myofibrils, and the non-sarcomeric cytoskeleton, which is composed of β- and γ-actin, microtubules, and intermediate filaments. Together, microtubules and intermediate filaments form a cross-linked scaffold, and these networks are responsible for the delivery of intracellular cargo, the transmission of mechanical signals, the shaping of membrane systems, and the organization of myofibrils and organelles. Microtubules are extensively altered as part of both adaptive and pathological cardiac remodeling, which has diverse ramifications for the structure and function of the cardiomyocyte. In heart failure, the proliferation and post-translational modification of the microtubule network is linked to a number of maladaptive processes, including the mechanical impediment of cardiomyocyte contraction and relaxation. This raises the possibility that reversing microtubule alterations could improve cardiac performance, yet therapeutic efforts will strongly benefit from a deeper understanding of basic microtubule biology in the heart. The aim of this review is to summarize the known physiological roles of the cardiomyocyte microtubule network, the consequences of its pathological remodeling, and to highlight the open and intriguing questions regarding cardiac microtubules.
Advancements in cell biological and biophysical approaches and super-resolution imaging have greatly broadened our view of tubulin biology over the last decade. In the heart, microtubules and microtubule-based transport help to organize and maintain key structures within the cardiomyocyte, including the sarcomere, intercalated disc, protein clearance machinery and transverse-tubule and sarcoplasmic reticulum membranes. It has become increasingly clear that post translational regulation of microtubules is a key determinant of their sub-cellular functionality. Alterations in microtubule network density, stability, and post-translational modifications are hallmarks of pathological cardiac remodeling, and modified microtubules can directly impede cardiomyocyte contractile function in various forms of heart disease. This review summarizes the functional roles and multi-leveled regulation of the cardiac microtubule cytoskeleton and highlights how refined experimental techniques are shedding mechanistic clarity on the regionally specified roles of microtubules in cardiac physiology and pathophysiology.
心肌细胞是大型(约 40000 µm)的、杆状的肌肉细胞,为每次心跳提供动力。这些高度结构化的细胞充满了密集的细胞骨架网络,可以分为两组——收缩(即肌节)细胞骨架,由丝状肌动蛋白-肌球蛋白阵列组成的肌原纤维组成,和非肌节细胞骨架,由β和γ肌动蛋白、微管和中间丝组成。微管和中间丝共同形成交联支架,这些网络负责细胞内货物的输送、机械信号的传递、膜系统的成形以及肌原纤维和细胞器的组织。微管作为适应性和病理性心脏重塑的一部分发生广泛改变,对心肌细胞的结构和功能有多种影响。在心力衰竭中,微管网络的增殖和翻译后修饰与许多适应性不良过程有关,包括心肌细胞收缩和松弛的机械障碍。这就提出了一种可能性,即逆转微管改变可能改善心脏功能,但治疗努力将从深入了解心脏中的基本微管生物学中受益匪浅。本综述的目的是总结心肌细胞微管网络的已知生理作用、其病理性重塑的后果,并强调心脏微管的悬而未决和有趣的问题。
在过去十年中,细胞生物学和生物物理方法的进步以及超分辨率成像极大地拓宽了我们对微管生物学的认识。在心脏中,微管和基于微管的运输有助于组织和维持心肌细胞中的关键结构,包括肌节、闰盘、蛋白质清除机制以及横管和肌浆网膜。越来越清楚的是,微管的翻译后调节是其亚细胞功能的关键决定因素。微管网络密度、稳定性和翻译后修饰的改变是病理性心脏重塑的标志,改变的微管可以直接阻碍各种形式心脏病中心肌细胞的收缩功能。本综述总结了心脏微管细胞骨架的功能作用和多层次调节,并强调了精细的实验技术如何为微管在心脏生理学和病理生理学中的区域特异性作用提供机制上的清晰认识。