Laboratory of Systems Biology, Department of Cybernetics, Tallinn University of Technology, Akadeemia 15, room SCI-218, 12618 Tallinn, Estonia.
Philos Trans R Soc Lond B Biol Sci. 2022 Nov 21;377(1864):20210321. doi: 10.1098/rstb.2021.0321. Epub 2022 Oct 3.
The ontogeny of the heart describes its development from the fetal to the adult stage. In newborn mammals, blood pressure and thus cardiac performance are relatively low. The cardiomyocytes are thin, and with a central core of mitochondria surrounded by a ring of myofilaments, while the sarcoplasmic reticulum (SR) is sparse. During development, as blood pressure and performance increase, the cardiomyocytes become more packed with structures involved in excitation-contraction (e-c) coupling (SR and myofilaments) and the generation of ATP (mitochondria) to fuel the contraction. In parallel, the e-c coupling relies increasingly on calcium fluxes through the SR, while metabolism relies increasingly on fatty acid oxidation. The development of transverse tubules and SR brings channels and transporters interacting via calcium closer to each other and is crucial for e-c coupling. However, for energy transfer, it may seem counterintuitive that the increased structural density restricts the overall ATP/ADP diffusion. In this review, we discuss how this is because of the organization of all these structures forming modules. Although the overall diffusion across modules is more restricted, the energy transfer within modules is fast. A few studies suggest that in failing hearts this modular design is disrupted, and this may compromise intracellular energy transfer. This article is part of the theme issue 'The cardiomyocyte: new revelations on the interplay between architecture and function in growth, health, and disease'.
心脏的个体发生描述了它从胎儿到成人阶段的发育过程。在新生哺乳动物中,血压相对较低,因此心脏功能也相对较低。心肌细胞较薄,其中央核心是线粒体,周围环绕着一圈肌丝,而肌浆网(SR)则较为稀疏。在发育过程中,随着血压和性能的提高,心肌细胞变得更加密集,其中涉及兴奋-收缩(e-c)偶联(SR 和肌丝)和产生 ATP(线粒体)以提供收缩动力的结构也更加密集。与此同时,e-c 偶联越来越依赖于通过 SR 的钙通量,而代谢则越来越依赖于脂肪酸氧化。横小管和 SR 的发育使通过钙相互作用的通道和转运蛋白彼此更接近,这对 e-c 偶联至关重要。然而,对于能量转移来说,结构密度的增加会限制整体 ATP/ADP 扩散,这似乎违反直觉。在这篇综述中,我们讨论了为什么这是因为所有这些结构形成模块的组织方式。尽管模块之间的整体扩散受到更多限制,但模块内的能量转移速度很快。一些研究表明,在衰竭的心脏中,这种模块化设计被打乱,这可能会损害细胞内能量转移。本文是主题为“心肌细胞:在生长、健康和疾病中结构与功能相互作用的新发现”的一部分。