Bishopric Nanette H
Department of Molecular and Cellular Pharmacology, University of Miami, Miami, Florida 33101, USA.
Ann N Y Acad Sci. 2005 Jun;1047:13-29. doi: 10.1196/annals.1341.002.
This review provides an overview of the evolutionary path to the mammalian heart from the beginnings of life (about four billion years ago ) to the present. Essential tools for cellular homeostasis and for extracting and burning energy are still in use and essentially unchanged since the appearance of the eukaryotes. The primitive coelom, characteristic of early multicellular organisms ( approximately 800 million years ago), is lined by endoderm and is a passive receptacle for gas exchange, feeding, and sexual reproduction. The cells around this structure express genes homologous to NKX2.5/tinman, and gradual specialization of this "gastroderm" results in the appearance of mesoderm in the phylum Bilateria, which will produce the first primitive cardiac myocytes. Investment of the coelom by these mesodermal cells forms a "gastrovascular" structure. Further evolution of this structure in the bilaterian branches Ecdysoa (Drosophila) and Deuterostoma (amphioxus) culminate in a peristaltic tubular heart, without valves, without blood vessels or blood, but featuring a single layer of contracting mesoderm. The appearance of Chordata and subsequently the vertebrates is accompanied by a rapid structural diversification of this primitive linear heart: looping, unidirectional circulation, an enclosed vasculature, and the conduction system. A later innovation is the parallel circulation to the lungs, followed by the appearance of septa and the four-chambered heart in reptiles, birds, and mammals. With differentiation of the cardiac chambers, regional specialization of the proteins in the cardiac myocyte can be detected in the teleost fish and amphibians. In mammals, growth constraints are placed on the heart, presumably to accommodate the constraints of the body plan and the thoracic cavity, and adult cardiac myocytes lose the ability to re-enter the cell cycle on demand. Mammalian cardiac myocyte innervation betrays the ancient link between the heart, the gut, and reproduction: the vagus nerve controlling heart rate emanates from centers in the central nervous system regulating feeding and affective behavior.
本综述概述了从生命起源(约40亿年前)到现在哺乳动物心脏的进化历程。自真核生物出现以来,细胞内稳态以及能量提取和消耗所必需的工具仍在使用,且基本未变。早期多细胞生物(约8亿年前)特有的原始体腔由内胚层排列,是气体交换、进食和有性生殖的被动容器。围绕该结构的细胞表达与NKX2.5/ tinman同源的基因,这种“胃皮”的逐渐特化导致两侧对称动物门中中胚层的出现,中胚层将产生第一批原始心肌细胞。这些中胚层细胞对体腔的包绕形成了一个“胃肠血管”结构。在蜕皮动物(果蝇)和后口动物(文昌鱼)这两个两侧对称动物分支中,该结构的进一步进化最终形成了蠕动的管状心脏,没有瓣膜,没有血管或血液,但有单层收缩中胚层。脊索动物以及随后脊椎动物的出现伴随着这种原始线性心脏的快速结构多样化:心脏环化、单向循环、封闭的脉管系统和传导系统。后来的一项创新是与肺的并行循环,随后在爬行动物、鸟类和哺乳动物中出现了隔膜和四腔心脏。随着心腔的分化,在硬骨鱼和两栖动物中可以检测到心肌细胞中蛋白质的区域特化。在哺乳动物中,心脏受到生长限制,大概是为了适应身体结构和胸腔的限制,成年心肌细胞失去了按需重新进入细胞周期的能力。哺乳动物心肌细胞的神经支配揭示了心脏、肠道和生殖之间古老的联系:控制心率的迷走神经起源于调节进食和情感行为的中枢神经系统中心。