THE DORSAL AORTAE, Which Run with the Long Axis of the Embryo and Form the Continuation of the Endocardial Heart Tubes
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THE DORSAL AORTAE, Which Run with the Long Axis of the Embryo and Form the Continuation of the Endocardial Heart Tubes
AORTIC ARCH SYSTEM The major arteries in an early embryo are represented by a pair of vessels THE DORSAL AORTAE, which run with the long axis of the embryo and form the continuation of the endocardial heart tubes. The cranial portion of each dorsal aorta forms an arc on both sides of the foregut, thus establishing the first pair of aortic arch arteries, termed aortic arches Dr. Amjad Shatarat, School of Medicine, 1 The University of Jordan Arterial System • Aortic Arches • they run within branchial (pharyngeal) arches • These arteries, the aortic arches, arise from the aortic sac, the most distal part of the truncus arteriosus . • The aortic sac, giving rise to a total of five pairs of arteries. • The pharyngeal arches and their vessels appear in a cranial-to-caudal sequence, so that they are not all present simultaneously. • Consequently, the five arches are numbered I, II, III, IV, and VI . • During further development, this arterial pattern becomes modified, and some vessels regress completely. Dr. Amjad Shatarat, School of Medicine, 2 The University of Jordan • Division of the truncus arteriosus by the aorticopulmonary septum divides the outflow channel of the heart into the ventral aorta and the pulmonary trunk. The aortic sac then forms right and left horns, which subsequently give rise to the brachiocephalic artery and the proximal segment of the aortic arch, respectively . Dr. Amjad Shatarat, School of Medicine, 3 The University of Jordan The first pair of arteries largely disappears but remnants of them form part of the maxillary arteries, which supply the ears, teeth, and muscles of the eyes and face Derivatives of Second Pair of Pharyngeal Arch Arteries Dorsal parts of these arteries persist and form the stems of the small stapedial arteries; these small vessels run through the ring of the stapes, a small bone in the middle ear Dr. -
Fetal Blood Flow and Genetic Mutations in Conotruncal Congenital Heart Disease
Journal of Cardiovascular Development and Disease Review Fetal Blood Flow and Genetic Mutations in Conotruncal Congenital Heart Disease Laura A. Dyer 1 and Sandra Rugonyi 2,* 1 Department of Biology, University of Portland, Portland, OR 97203, USA; [email protected] 2 Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA * Correspondence: [email protected] Abstract: In congenital heart disease, the presence of structural defects affects blood flow in the heart and circulation. However, because the fetal circulation bypasses the lungs, fetuses with cyanotic heart defects can survive in utero but need prompt intervention to survive after birth. Tetralogy of Fallot and persistent truncus arteriosus are two of the most significant conotruncal heart defects. In both defects, blood access to the lungs is restricted or non-existent, and babies with these critical conditions need intervention right after birth. While there are known genetic mutations that lead to these critical heart defects, early perturbations in blood flow can independently lead to critical heart defects. In this paper, we start by comparing the fetal circulation with the neonatal and adult circulation, and reviewing how altered fetal blood flow can be used as a diagnostic tool to plan interventions. We then look at known factors that lead to tetralogy of Fallot and persistent truncus arteriosus: namely early perturbations in blood flow and mutations within VEGF-related pathways. The interplay between physical and genetic factors means that any one alteration can cause significant disruptions during development and underscore our need to better understand the effects of both blood flow and flow-responsive genes. -
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FIG. 4–1 Dorsal aspect of the 10-somite embryo. 24 IV the fourth week of life somite and neural tube period I. EMBRYO PROPER caudal openings of the tube are called neuropores. The rostral neuropore closes between 18 and 20 somites. The caudal neuro- A. EXTERNAL APPEARANCE pore closes at 25 somites. Figs. 4–1, 4–2 1. The specimens measure approximately 1 to 3.5 mm in length Brain and have 1 to 29 pairs of somites. Three brain subdivisions are present in the cranial portion of the 2. The head and tail folds move the attachment of the amnion tube and are named, from cranial to caudal, the prosencephalon, to the ventral side of the head and tail regions, respectively. mesencephalon and rhombencephalon. The boundary between the The lateral body folds move the amnion attachment to the pros- and mesencephalon is demarcated by a ventral bend, called ventrolateral surface in the midportion of the embryo. the cephalic flexure. An external groove and a prominent swelling 3. The head region is elevated above the yolk sac by the large on the medial surface of the neural plate may also demarcate the pericardial sac, the midportion lies upon the yolk sac and the boundary. The boundary between the mes- and rhombencephalon caudal region is curved toward the yolk sac. is distinguished by a groove on the medial and lateral surfaces of 4. The embryo possesses somites, which are apparent through the neural plate or tube. the ectoderm. 5. The neural tube develops from the neural plate and remains Prosencephalon open at each end for 2 to 4 days. -
Endothelium in the Pharyngeal Arches 3, 4 and 6 Is Derived from the Second Heart Field
Thomas Jefferson University Jefferson Digital Commons Center for Translational Medicine Faculty Papers Center for Translational Medicine 1-15-2017 Endothelium in the pharyngeal arches 3, 4 and 6 is derived from the second heart field. Xia Wang Thomas Jefferson University Dongying Chen Thomas Jefferson University Kelley Chen Thomas Jefferson University Ali Jubran Thomas Jefferson University AnnJosette Ramirez Thomas Jefferson University Follow this and additional works at: https://jdc.jefferson.edu/transmedfp Part of the Translational Medical Research Commons LetSee next us page know for additional how authors access to this document benefits ouy Recommended Citation Wang, Xia; Chen, Dongying; Chen, Kelley; Jubran, Ali; Ramirez, AnnJosette; and Astrof, Sophie, "Endothelium in the pharyngeal arches 3, 4 and 6 is derived from the second heart field." (2017). Center for Translational Medicine Faculty Papers. Paper 45. https://jdc.jefferson.edu/transmedfp/45 This Article is brought to you for free and open access by the Jefferson Digital Commons. The Jefferson Digital Commons is a service of Thomas Jefferson University's Center for Teaching and Learning (CTL). The Commons is a showcase for Jefferson books and journals, peer-reviewed scholarly publications, unique historical collections from the University archives, and teaching tools. The Jefferson Digital Commons allows researchers and interested readers anywhere in the world to learn about and keep up to date with Jefferson scholarship. This article has been accepted for inclusion in Center for Translational Medicine Faculty Papers by an authorized administrator of the Jefferson Digital Commons. For more information, please contact: [email protected]. Authors Xia Wang, Dongying Chen, Kelley Chen, Ali Jubran, AnnJosette Ramirez, and Sophie Astrof This article is available at Jefferson Digital Commons: https://jdc.jefferson.edu/transmedfp/45 HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author Dev Biol Manuscript Author . -
Fate of the Mammalian Cardiac Neural Crest
Development 127, 1607-1616 (2000) 1607 Printed in Great Britain © The Company of Biologists Limited 2000 DEV4300 Fate of the mammalian cardiac neural crest Xiaobing Jiang1,3, David H. Rowitch4,*, Philippe Soriano5, Andrew P. McMahon4 and Henry M. Sucov2,3,‡ Departments of 1Biological Sciences and 2Cell & Neurobiology, 3Institute for Genetic Medicine, Keck School of Medicine, University of Southern California, 2250 Alcazar St., IGM 240, Los Angeles, CA 90033, USA 4Department of Molecular and Cell Biology, Harvard University, 16 Divinity Ave., Cambridge, MA 02138, USA 5Program in Developmental Biology, Division of Basic Sciences, A2-025, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, PO Box 19024, Seattle, WA 98109, USA *Present address: Department of Pediatric Oncology, Dana Farber Cancer Institute, 44 Binney St., Boston, MA 02115, USA ‡Author for correspondence (e-mail: [email protected]) Accepted 26 January; published on WWW 21 March 2000 SUMMARY A subpopulation of neural crest termed the cardiac neural of these vessels. Labeled cells populate the crest is required in avian embryos to initiate reorganization aorticopulmonary septum and conotruncal cushions prior of the outflow tract of the developing cardiovascular to and during overt septation of the outflow tract, and system. In mammalian embryos, it has not been previously surround the thymus and thyroid as these organs form. experimentally possible to study the long-term fate of this Neural-crest-derived mesenchymal cells are abundantly population, although there is strong inference that a similar distributed in midgestation (E9.5-12.5), and adult population exists and is perturbed in a number of genetic derivatives of the third, fourth and sixth pharyngeal arch and teratogenic contexts. -
Cardiovascular System Heart Development Cardiovascular System Heart Development
Cardiovascular System Heart Development Cardiovascular System Heart Development In human embryos, the heart begins to beat at approximately 22-23 days, with blood flow beginning in the 4th week. The heart is one of the earliest differentiating and functioning organs. • This emphasizes the critical nature of the heart in distributing blood through the vessels and the vital exchange of nutrients, oxygen, and wastes between the developing baby and the mother. • Therefore, the first system that completes its development in the embryo is called cardiovascular system. https://www.slideshare.net/DrSherifFahmy/intraembryonic-mesoderm-general-embryology Mesoderm is one of the three • Connective tissue primary germ layers that • Smooth and striated muscle • Cardiovascular System differentiates early in • Kidneys development that collectively • Spleen • Genital organs, ducts gives rise to all subsequent • Adrenal gland cortex tissues and organs. The cardiovascular system begins to develop in the third week of gestation. Blood islands develop in the newly formed mesoderm, and consist of (a) a central group of haemoblasts, the embryonic precursors of blood cells; (b) endothelial cells. Development of the heart and vascular system is often described together as the cardiovascular system. Development begins very early in mesoderm both within (embryonic) and outside (extra embryonic, vitelline, umblical and placental) the embryo. Vascular development occurs in many places. • Blood islands coalesce to form a vascular plexus. Preferential channels form arteries and veins. • Day 17 - Blood islands form first in the extra-embryonic mesoderm • Day 18 - Blood islands form next in the intra-embryonic mesoderm • Day 19 - Blood islands form in the cardiogenic mesoderm and coalesce to form a pair of endothelial heart tubes Development of a circulation • A circulation is established during the 4th week after the myocardium is differentiated. -
Congenital Abnormalities of the Aortic Arch: Revisiting the 1964 Stewart
Cardiovascular Pathology 39 (2019) 38–50 Contents lists available at ScienceDirect Cardiovascular Pathology Review Article Congenital abnormalities of the aortic arch: revisiting the 1964 ☆ Stewart classification Shengli Li a,⁎,HuaxuanWena,MeilingLianga,DandanLuoa, Yue Qin a,YimeiLiaoa, Shuyuan Ouyang b, Jingru Bi a, Xiaoxian Tian c, Errol R. Norwitz d,GuoyangLuoe,⁎⁎ a Department of Ultrasound, Shenzhen Maternity & Child Healthcare Hospital, Affiliated to Southern Medical University, Shenzhen, 518028, China b Department of Laboratory Medicine, Shenzhen Maternity & Child Healthcare Hospital, Affiliated to Southern Medical University, Shenzhen, 518028, China c Department of Ultrasound, Maternity & Child Healthcare Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, 538001, China d Department of Obstetrics & Gynecology, Tufts University School of Medicine, Boston, MA 02111 e Department of Obstetrics & Gynecology, Howard University, College of Medicine, Washington, DC 20060, USA article info abstract Article history: The traditional classification of congenital aortic arch abnormalities was described by James Stewart and col- Received 12 June 2018 leagues in 1964. Since that time, advances in diagnostic imaging technology have led to better delineation of Received in revised form 27 November 2018 the vasculature anatomy and the identification of previously unrecognized and unclassified anomalies. In this Accepted 28 November 2018 manuscript, we review the existing literature and propose a series of modifications to the original Stewart -
Development of the Vascular System in Five to Twenty-One
THE DEVELOPMENT OF THE VASCULAR SYSTEM IN FIVE TO TWtNTY-ONE SOMITE DOG EMBRYOS by ELDEN WILLIAM MARTIN B, S., Kansas State College of Agriculture and ADolied Science, 195>U A THESIS submitted in partial fulfillment of the requirements for the degree MASTER OF SCIENCE Department of Zoology KANSAS STATV: COLLEGE OF AGRICULTURE AND A PLIED SCIENCE 1958 LP TH Ooco/*>*Tv TABLE OF CONTENTS INTRO IXJ CTION AND LITERATURE REVIEW 1 MATERIALS AND METHODS ^ OBSERVATIONS 6 Five-Somi te Stag© . 6 Seven-Somite Stage 8 Eight-Somite Stage 9 Ten- and bleven-Somite Stage 12 Twe 1 ve-Somi te Stage • \\i Fifteen-Somite Stage 18 Seventeen-Somite Stage 21 Eighteen-Somite Stage 2$ Twenty- and Twenty- one -Somite Stage 27 INTERPRETATIONS AND DISCUSSION 30 Vasculogenesis • 30 Cardiogenesis 33 The Origin and Development of Arteries \ 3lj. Aortic Arches •••« 3I4. Cranial Arterie s ...•• 36 The Dorsal Aorta 37 Intersegmental AAteries 39 Vertebral Arteries 39 Vitelline Arteries }±q The Allantoic Artery \±\ Ill IITERPRETATION AND DISCUSSION (Contd.) The Origin and Development of Veins •• kl The Anterior Cardinal Veins . I4.I Posterior Cardinal Veins k2 Umbilical Veins U3 Common Cardinal Veins kh Interconnecting Vessels Ui> SUMMARY kl LITERA°URE CITED $1 ACKNOWLEDGMENTS 53 APPENDIX 5U HTmDUCTIOW AND LITFRATORF. rfvibw While the dog has been employed extensively as a labora- tory animal in various fields of scientific endeavour, the use of this animal in embryology has been neglected. As a con- sequence, the literature on the circulatory system of the dog was represented only by an unpublished thesis by Duffey (3) on oardlogenesis and the first heart movements. -
Cardiovascular System Note: the Cardiovascular System Develops Early (Week 3), Enabling the Embryo to Grow Beyond the Short
Lymphatics: Lymph vessel formation is similar to blood angiogenesis. Lymphatics begin as lymph sacs in three regions: jugular (near brachiocephalic veins); cranial abdominal (future cysterna chyla); and iliac region. Lym- phatic vessels (ducts) form as outgrowths of the sacs. mesenchyme Lymph nodes are produced by localized mesoder- sinusoid lymph duct lumen mal invaginations that partition the vessel lumen into sinu- soids. The mesoderm develops a reticular framework within which mesodermal lymphocytes accumulate. The spleen and hemal nodes (in ruminants) invagination develop similar to the way lymph nodes develop. Lymph Node Formation Prior to birth, fetal circulation is designed for an in utero aqueous environment where the pla- centa oxygenates fetal blood. Suddenly, at birth... Three In-Utero Adjustments ductus Stretching and constriction of arteriosus umbilical arteries shifts fetal blood flow aortic arch from the placenta to the fetus. Reduced pulmonary trunk L atrium venous return through the (left) umbili- foramen ovale R cal vein and ductus venosus allows the atrium latter to gradually close (over a period caudal vena cava of days). Bradykinin released by expand- ductus venosus ing lungs and increased oxygen concen- tration in blood triggers constriction of aorta the ductus arteriosus which, over two liver months, is gradually converted to a fibrous structure, the ligamentum arte- umbilical v. riosum. portal v. The increased blood flow to the lungs and then to the left atrium equalizes pres- sure in the two atria, resulting in closure umbilical aa. of the foramen ovale that eventually grows permanent. 29 The cardiogenic area, the place where the embryonic heart originates, is located . -
Cardiac Development Cardiac Development
CARDIAC DEVELOPMENT CARDIAC DEVELOPMENT Diane E. Spicer, BS, PA(ASCP) University of Florida Dept. of Pediatric Cardiology Curator – Van Mierop Cardiac Archive This lecture is given with special thanks to Professor RH Anderson, my mentor and my friend. Without his spectacular research and images of both human and mouse embryos, this lecture would not have been possible. CARDIAC DEVELOPMENT CARDIAC DEVELOPMENT ♥ What’s new? ♥ “An understanding of the elementary facts of human and comparative embryology is essential to an intelligent grasp of the ontogenetic problems of congenital cardiac disease.” ♥ Maude Abbott “Atlas of Congenital Cardiac Disease” American Heart Association, New York, 1936 CARDIACCARDIAC DEVELOPMENTDEVELOPMENT ♥ Do we need to change? ♥ In the past, most theories of morphogenesis were based on fanciful interpretation of normal development ♥ We are now able to demonstrate the anatomic and molecular changes that take place during cardiac development ♥ This now permits us to base our inferences on evidence, rather than speculation CARDIACCARDIAC DEVELOPMENTDEVELOPMENT ♥ It used to be thought that all components of the postnatal heart were contained within the initial linear heart tube ♥ In reality, new material is added at the arterial and venous poles from the second heart field. The initial tube, derived from the first heart field, forms little more than the definitive left ventricle Mouse embryo – 9 somites – Myosin LC Growth at arterial pole Putative left ventricle Growth at venous pole Mouse embryo – E8.5 – 9 somites -
6 Development of the Great Vessels and Conduction Tissue
Development of the Great Vessels and Conduc6on Tissue Development of the heart fields • h:p://php.med.unsw.edu.au/embryology/ index.php?6tle=Advanced_-_Heart_Fields ! 2 Septa6on of the Bulbus Cordis Bulbus Cordis AV Canal Ventricle Looking at a sagital sec6on of the heart early in development the bulbus cordis is con6nuous with the ventricle which is con6nuous with the atria. As the AV canal shiOs to the right the bulbus move to the right as well. Septa6on of the Bulbus Cordis A P A P The next three slides make the point via cross sec6ons that the aorta and pulmonary arteries rotate around each other. This means the septum between them changes posi6on from superior to inferior as well. Septa6on of the Bulbus Cordis P A A P Septa6on of the Bulbus Cordis P A P A Migra6on of neural crest cells Neural crest cells migrate from the 3ed, 4th and 6th pharyngeal arches to form some of the popula6on of cells forming the aor6copulmonary septum. Septa6on of the Bulbus Cordis Truncal (Conal) Swellings Bulbus Cordis The cardiac jelly in the region of the truncus and conus adds the neural crest cells and expands as truncal swellings. Septa6on of the Bulbus Cordis Aorticopulmonary septum These swellings grow toward each other to meet and form the septum between the aorta and pulmonary artery. Aorta Pulmonary Artery Septa6on of the Bulbus Cordis Anterior 1 2 3 1 2 3 The aor6copulmonary septum then rotates as it moves inferiorly. However, the exact mechanism for that rota6on remains unclear. Septa6on of the Bulbus Cordis Aorta Pulmonary Artery Conal Ridges IV Foramen Membranous Muscular IV Endocarial Septum Interventricular Cushion Septum However, the aor6copulmonary septum must form properly for the IV septum to be completed. -
Human Placenta Is a Potent Hematopoietic Niche Containing Hematopoietic Stem and Progenitor Cells Throughout Development
Cell Stem Cell Article Human Placenta Is a Potent Hematopoietic Niche Containing Hematopoietic Stem and Progenitor Cells throughout Development Catherine Robin,1,5 Karine Bollerot,1,5 Sandra Mendes,1 Esther Haak,1 Mihaela Crisan,1 Francesco Cerisoli,1 Ivoune Lauw,1 Polynikis Kaimakis,1 Ruud Jorna,1 Mark Vermeulen,3 Manfred Kayser,3 Reinier van der Linden,1 Parisa Imanirad,1 Monique Verstegen,2 Humaira Nawaz-Yousaf,1 Natalie Papazian,2 Eric Steegers,4 Tom Cupedo,2 and Elaine Dzierzak1,* 1Erasmus MC Stem Cell Institute, Department of Cell Biology 2Department of Hematology 3Department of Forensic Molecular Biology 4Department of Obstetrics and Gynecology Erasmus University Medical Center, 3000 CA Rotterdam, the Netherlands 5These authors contributed equally to this work *Correspondence: [email protected] DOI 10.1016/j.stem.2009.08.020 SUMMARY becomes hematopoietic. The emergence of multipotent progen- itors and HSCs, organized in clusters of cells closely adherent to Hematopoietic stem cells (HSCs) are responsible for the ventral wall of the dorsal aorta, starts at day 27 in the devel- the life-long production of the blood system and are oping splanchnopleura/AGM region (Tavian et al., 1996, 1999, pivotal cells in hematologic transplantation thera- 2001). Starting at day 30, the first erythroid progenitors (BFU- pies. During mouse and human development, the E, burst forming unit erythroid) are found in the liver, with multi- first HSCs are produced in the aorta-gonad-meso- lineage hematopoietic progenitors (CFU-Mix or -GEMM; colony nephros region. Subsequent to this emergence, forming unit granulocyte, erythroid, macrophage, megakaryo- cyte) appearing in this tissue at week 13 (Hann et al., 1983).