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      Coronary artery established through amniote evolution

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          Abstract

          Coronary arteries are a critical part of the vascular system and provide nourishment to the heart. In humans, even minor defects in coronary arteries can be lethal, emphasizing their importance for survival. However, some teleosts survive without coronary arteries, suggesting that there may have been some evolutionary changes in the morphology and function of coronary arteries in the tetrapod lineage. Here, we propose that the true ventricular coronary arteries were newly established during amniote evolution through remodeling of the ancestral coronary vasculature. In mouse ( Mus musculus) and Japanese quail ( Coturnix japonica) embryos, the coronary arteries unique to amniotes are established by the reconstitution of transient vascular plexuses: aortic subepicardial vessels (ASVs) in the outflow tract and the primitive coronary plexus on the ventricle. In contrast, amphibians ( Hyla japonica, Lithobates catesbeianus, Xenopus laevis, and Cynops pyrrhogaster) retain the ASV-like vasculature as truncal coronary arteries throughout their lives and have no primitive coronary plexus. The anatomy and development of zebrafish ( Danio rerio) and chondrichthyans suggest that their hypobranchial arteries are ASV-like structures serving as the root of the coronary vasculature throughout their lives. Thus, the ventricular coronary artery of adult amniotes is a novel structure that has acquired a new remodeling process, while the ASVs, which occur transiently during embryonic development, are remnants of the ancestral coronary vessels. This evolutionary change may be related to the modification of branchial arteries, indicating considerable morphological changes underlying the physiological transition during amniote evolution.

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          Coronary arteries are tasked with supplying the heart with oxygenated blood and nutrients. Any blockage or developmental problem in these blood vessels can have severe and sometimes lethal consequences. Due to their importance for health, researchers have extensively studied how coronary arteries form in humans and mice; a more limited range of studies have also looked at their equivalent in zebrafish. However, little is known about these structures develop in animals such as birds, amphibians, or other groups of fish. This makes it difficult to retrace the evolutionary processes that have given rise to the coronary arteries we are familiar with in mammals.

          To address this knowledge gap, Mizukami et al. set out to compare blood vessel development around the heart of mammals, birds, amphibians, and fish. To do this, they performed detailed anatomical studies of blood vessel structure at different stages of development in mice as well as quail, frogs and newts, zebrafish and sharks.

          In both mice and quail, small arterial subepicardial vessels (or ASVs) emerged early in development around the heart; these subsequently reorganised and remodelled themselves to give rise to the ‘true’ coronary arteries characteristic of the mature heart.

          Frogs and newts also developed similar ASV-like structures; however, unlike their mammalian and bird equivalents, these vessels did not reorganise, instead being retained into adulthood. In fish, blood vessel development resembled that of amphibians, suggesting that the coronary artery-like structures seen in some fish are an ‘ancestral’ form of ASVs, rather than the equivalent of the mature coronary arteries in mammals and birds.

          This work sheds light on the evolutionary processes shaping essential structures in the heart. In the future, Mizukami et al. hope that this knowledge will help develop a greater range of experimental animal models for studying heart disease and potential treatments.

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          Most cited references79

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          Stages of embryonic development of the zebrafish.

          We describe a series of stages for development of the embryo of the zebrafish, Danio (Brachydanio) rerio. We define seven broad periods of embryogenesis--the zygote, cleavage, blastula, gastrula, segmentation, pharyngula, and hatching periods. These divisions highlight the changing spectrum of major developmental processes that occur during the first 3 days after fertilization, and we review some of what is known about morphogenesis and other significant events that occur during each of the periods. Stages subdivide the periods. Stages are named, not numbered as in most other series, providing for flexibility and continued evolution of the staging series as we learn more about development in this species. The stages, and their names, are based on morphological features, generally readily identified by examination of the live embryo with the dissecting stereomicroscope. The descriptions also fully utilize the optical transparancy of the live embryo, which provides for visibility of even very deep structures when the embryo is examined with the compound microscope and Nomarski interference contrast illumination. Photomicrographs and composite camera lucida line drawings characterize the stages pictorially. Other figures chart the development of distinctive characters used as staging aid signposts.
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            Whole-brain imaging with single-cell resolution using chemical cocktails and computational analysis.

            Systems-level identification and analysis of cellular circuits in the brain will require the development of whole-brain imaging with single-cell resolution. To this end, we performed comprehensive chemical screening to develop a whole-brain clearing and imaging method, termed CUBIC (clear, unobstructed brain imaging cocktails and computational analysis). CUBIC is a simple and efficient method involving the immersion of brain samples in chemical mixtures containing aminoalcohols, which enables rapid whole-brain imaging with single-photon excitation microscopy. CUBIC is applicable to multicolor imaging of fluorescent proteins or immunostained samples in adult brains and is scalable from a primate brain to subcellular structures. We also developed a whole-brain cell-nuclear counterstaining protocol and a computational image analysis pipeline that, together with CUBIC reagents, enable the visualization and quantification of neural activities induced by environmental stimulation. CUBIC enables time-course expression profiling of whole adult brains with single-cell resolution. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Genetics of coronary artery disease: discovery, biology and clinical translation

              The past decade has seen tremendous progress in understanding the genetic architecture of coronary artery disease (CAD). Khera and Kathiresan review research efforts that have improved our understanding of the genetic drivers of CAD, and discuss the promises and challenges of integrating genetic information into routine clinical practice.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                22 August 2023
                2023
                : 12
                : e83005
                Affiliations
                [1 ] Department of Physiological Chemistry and Metabolism, Graduate School of Medicine, The University of Tokyo ( https://ror.org/057zh3y96) Tokyo Japan
                [2 ] Developmental Cardiology Laboratory, International Research Center for Medical Science, Kumamoto University ( https://ror.org/02cgss904) Kumamoto Japan
                [3 ] Department of Molecular Pathophysiology, Institute of Advanced Medical Sciences, Nippon Medical School ( https://ror.org/00krab219) Tokyo Japan
                [4 ] School of Pharmacy, Kitasato University ( https://ror.org/00f2txz25) Tokyo Japan
                [5 ] Institute of Applied Physics, University of Tsukuba ( https://ror.org/02956yf07) Tsukuba Japan
                [6 ] Congenital Anomaly Research Center, Kyoto University Graduate School of Medicine ( https://ror.org/02kpeqv85) Kyoto Japan
                [7 ] Molecular Craniofacial Embryology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University ( https://ror.org/051k3eh31) Tokyo Japan
                [8 ] Faculty of Life Sciences, Department of Applied Biosciences, Toyo University ( https://ror.org/059d6yn51) Gunma Japan
                [9 ] Heart Center, Department of Pediatric Cardiology, Tokyo Women’s Medical University ( https://ror.org/03kjjhe36) Tokyo Japan
                [10 ] Department of Animal Nursing Science, Yamazaki University of Animal Health Technology ( https://ror.org/04gzb3214) Tokyo Japan
                Stanford University ( https://ror.org/00f54p054) United States
                Max Planck Institute for Heart and Lung Research ( https://ror.org/0165r2y73) Germany
                Stanford University ( https://ror.org/00f54p054) United States
                Stanford University ( https://ror.org/00f54p054) United States
                Stanford University ( https://ror.org/00f54p054) United States
                Author information
                https://orcid.org/0000-0003-1324-8139
                https://orcid.org/0000-0002-4152-5706
                Article
                83005
                10.7554/eLife.83005
                10444023
                37605519
                baf2f9b0-a504-4624-a250-c38caf9dc26f
                © 2023, Mizukami et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 26 August 2022
                : 17 July 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 20H04858
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 20K15858
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002241, Japan Science and Technology Agency;
                Award ID: PRESTO JP22715256
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 22K07877
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 19H01048
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 22H04991
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Developmental Biology
                Evolutionary Biology
                Custom metadata
                During the evolution of amniotes, the transformation of branchial arches coincided with the drastic remodeling of the ancestral extrinsic cardiac arteries, giving rise to novel ventricular coronary arteries that are unique to amniotes.

                Life sciences
                heart,cardiovascular,morphology,evo-devo,anatomy,mouse,xenopus,zebrafish,other
                Life sciences
                heart, cardiovascular, morphology, evo-devo, anatomy, mouse, xenopus, zebrafish, other

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