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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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. -
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. -
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 -
Study on Branching Pattern of Aortic Arch in Indian
Original Article http://dx.doi.org/10.5115/acb.2012.45.3.203 pISSN 2093-3665 eISSN 2093-3673 Study on branching pattern of aortic arch in Indian Sumit Tulshidas Patil, Meena M. Meshram, Namdeo Y. Kamdi, Arun P. Kasote, Madhukar P. Parchand Department of Anatomy, Government Medical College, Nagpur, Maharashtra, India Abstract: Knowledge of the branching pattern of aortic arch is important during supra-aortic angiography, aortic instrumentation, thoracic and neck surgery. The purpose of this study is to describe different branching pattern of arch of aorta in Indian subjects, in order to offer useful data to anatomists, radiologists, vascular surgeons while relating it to the embryological basis. Seventy five arches of adult Indian cadavers were exposed and their branches examined during cadaveric dissection in the Department of Anatomy, Government Medical College, Nagpur. The usual three-branched aortic arch was found in 58 cadavers (77.3%); the 11 (14.66%) remaining aortic arch showed only two branches, out of which one was a common trunk, which incorporated the brachiocephalic trunk and left common carotid and other left subclavian artery and 6 (8%) aortic arches showed direct arch origin of the left vertebral artery. Although the variations are usually asymptomatic, they may cause dyspnoea, dysphasia, intermittent claudication, misinterpretation of radiological examinations and complications during neck and thorax surgery. Knowledge of different patterns of arch of aorta is critical when invading the arch of aorta and its branches by instruments, as all these areas are delicate. Key words: Thoracic aorta, Variations, Branches, Vascular surgery Received March 28, 2012; Revised July 5, 2012; Accepted August 23, 2012 Introduction between them. -
Aortic Arches
Human Embryology: Heart Development II Kimara L. Targoff, M.D. Division of Pediatric Cardiology, Columbia University Medical Center Developmental Genetics Program, Skirball Institute, NYU School of Medicine Human Vascular Development • Overview • Aortic Arch Development • Arterial Vascular Development • Venous System Development • Lymphatic Development • Transition from Fetal to Post-Natal Circulation Development of the Arterial and Venous Systems Cranial Ends of the Dorsal Aortae Form a Dorsoventral Loop: The First Aortic Arch Aortic Arches Arise in a Craniocaudal Sequence Surrounding the Pharynx Aortic Arches Give Rise to Important Head, Neck, and Upper Thorax Vessels Aortic Arch Development in the Chick Embryo Fgf8 is Required for Pharyngeal Arch Development in Mouse Abu-Issa, R. et al., Development 2002. Cardiovascular and Thymic Defects in Tbx1 Hypomorphic Mutant Neonates Hu, T. et al., Development 2004. Aortic Arch Development Dorsal aorta 1 2 3 Ventral aorta 4 5 6 7 iseg Harsh Thaker Aortic Arch Development Dorsal aorta 1 2 3 Ventral aorta 4 5 6 7 iseg Harsh Thaker Aortic Arch and Derivatives 3 3 4 4 7 iseg 6 7 iseg 6 Aortic sac Truncus arteriosus Harsh Thaker Aortic Arch and Derivatives 3 3 4 4 7 iseg 6 7 iseg Harsh Thaker Aortic Arch and Derivatives 3 3 4 7 iseg 4 7 iseg 6 Harsh Thaker Aortic Arch and Derivatives RCC LCC RSC LSC BCA DA Harsh Thaker Recurrent Laryngeal Nerves RCC LCC RSC LSC BCA DA Harsh Thaker Defects in Normal Regression of the Arterial System Lead to Vascular Anomalies • Double Aortic Arch – Failure of the -
Vascular Endothelial Tyrosine Phosphatase (VE-PTP)-Null Mice Undergo Vasculogenesis but Die Embryonically Because of Defects in Angiogenesis
Vascular endothelial tyrosine phosphatase (VE-PTP)-null mice undergo vasculogenesis but die embryonically because of defects in angiogenesis Melissa G. Dominguez, Virginia C. Hughes, Li Pan, Mary Simmons, Christopher Daly, Keith Anderson, Irene Noguera-Troise, Andrew J. Murphy, David M. Valenzuela, Samuel Davis, Gavin Thurston, George D. Yancopoulos*, and Nicholas W. Gale* Regeneron Pharmaceuticals, Inc., 777 Old Saw Mill River Road, Tarrytown, NY 10591 Contributed by George D. Yancopoulos, December 28, 2006 (sent for review December 21, 2006) Development of the vascular system depends on the highly coordi- vascular endothelial PTP (VE-PTP) (4). VE-PTP, the mouse nated actions of a variety of angiogenic regulators. Several of these homologue of receptor-type human PTP- (5), has been shown to regulators are members of the tyrosine kinase superfamily, including associate with and dephosphorylate Tie2 (4) and VE-cadherin (6) VEGF receptors and angiopoietin receptors, Tie1 and Tie2. Tyrosine but was shown to not interact with VEGF-R2 (4). kinase signaling is counter-regulated by the activity of tyrosine To study the expression pattern in embryonic and adult tissues phosphatases, including vascular endothelial protein tyrosine phos- and to elucidate the functional role of VE-PTP in vascular devel- phatase (VE-PTP), which has previously been shown to modulate Tie2 opment, we generated mice in which the VE-PTP gene was activity. We generated mice in which VE-PTP is replaced with a replaced by LacZ, a high-resolution reporter gene. LacZ expression reporter gene. We confirm that VE-PTP is expressed in endothelium confirms that VE-PTP is expressed in both arterial and venous and also show that VE-PTP is highly expressed in the developing vascular endothelium in embryos, although more strongly in arterial outflow tract of the heart and later is expressed in developing heart vessels. -
Development of Heart Notes
Formation of heart tube: 3rd week Heart beat: 22nd –23rd day (beginning of fourth week) USG detection of heart beat: 7th week Foetal ECG: 11th week Endocardium from original heart tube Myocardium from surrounding mesoderm & epicardium (myoepicardial mantle) (visceral pericardium) Lining of pericardium epithelium of pericardial cavity Transverse sinus formed by disappearance of dorsal mesocardium (Present between arterial and venous ends of the heart tube) FATE Of SINUS VENOSUS Left horn of sinus venosus, along with medial part of common cardinal vein forms coronary sinus Lateral part of common cardinal vein forms oblique vein of left atrium Left venous valve merges with septum secundum. Right venous valve is divided in three parts by appearance of two transverse muscular bands, called limbic bands. i) The part above superior limbic band forms crista terminalis ii) The part between the two bands forms valve of inferior vena cava iii) The part below the inferior limbic band forms valve of coronary sinus INTERATRIAL SEPTUM i) Upper, thicker part is formed by septum secundum ii) Lower, thin part (floor of fossa ovalis) is formed by septum primum iii) Sharp margin of fossa ovalis is formed by lower, curved margin of septum secundum DEVELOPMENT OF RIGHT ATRIUM It develops from 1. Right half of primitive atrial chamber (rough part); 2. Absorption of right horn of sinus venosus (smooth part) and 3. Right atrioventricular canal. DEVELOPMENT OF LEFT ATRIUM It develops from 1. Left half of primitive atrial chamber (rough part – confined to the auricle); 2. Absorption of pulmonary veins (smooth part) and 3. Left atrioventricular canal. -
6. Heart and Circulatory System I
6. HEART AND CIRCULATORY SYSTEM I Dr. Taube P. Rothman P&S 12-520 [email protected] 212-305-7930 RECOMMENDED READING: Larsen Human Embryology, 3rd Edition, pp. 195-199; 157-169 top left; 172-174; bottom 181-182; 187-top 189, Simbryo-cardiovascular system SUMMARY: The circulatory system, consisting of heart, blood vessels, and blood cells is the first functional organ to develop. This lecture will focus on the formation of the embryonic vasculature, the origin and formation of the early heart tube and primitive cardiac chambers, cardiac looping, and the primitive circulation. Between the 5th - 8th week of embryonic development, the tubular heart is remodeled into a four chambered structure. We will see how right and left atrioventricular canals connect each atrium with its respective ventricle, and how the atrial septum and definitive right and left atria form. We will also see why the great veins deliver blood to the right atrium while the pulmonary veins empty into the left. GLOSSARY: Angioblasts: precursors of blood vessels Angiogenesis: lengthening, branching, sprouting and remodeling of embryonic blood vessels Aortic arches: paired arteries surrounding the pharynx; portions will contribute to formation of the great arterial vessels Blood islands: clusters of cells in the yolk sac, connecting stalk and chorionic villi that form primitive blood vessels Cardiac jelly: gelatinous extracellular matrix that forms the middle layer of the heart tube Ductus venosus: shunts most of the blood in the umbilical vein into the inferior vena cava -
Isl1-Expressing Non-Venous Cell Lineage Contributes to Cardiac Lymphatic Vessel Development
Developmental Biology 452 (2019) 134–143 Contents lists available at ScienceDirect Developmental Biology journal homepage: www.elsevier.com/locate/developmentalbiology Isl1-expressing non-venous cell lineage contributes to cardiac lymphatic vessel development Kazuaki Maruyama a, Sachiko Miyagawa-Tomita a,b,c, Kaoru Mizukami a, Fumio Matsuzaki d, Hiroki Kurihara a,e,* a Department of Physiological Chemistry and Metabolism, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan b Department of Pediatric Cardiology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan c Department of Animal Nursing Science, Yamazaki University of Animal Health Technology, 4-7-2 Minami-osawa, Hachioji, Tokyo, 192-0364, Japan d Laboratory for Cell Asymmetry, RIKEN Center for Developmental Biology, 2-2-3, Minatojiima-Minamimachi, Chuou-ku, Kobe, 650-0047, Japan e Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Chiyoda-ku, Tokyo, 102-0076, Japan ABSTRACT The origin of the mammalian lymphatic vasculature has been studied for more than a century; however, details regarding organ-specific lymphatic development remain unknown. A recent study reported that cardiac lymphatic endothelial cells (LECs) stem from venous and non-venous origins in mice. Here, we identified Isl1- expressing progenitors as a potential non-venous origin of cardiac LECs. Genetic lineage tracing with Isl1-Cre reporter mice suggested a possible contribution from the Isl1-expressing pharyngeal mesoderm constituting the second heart field to lymphatic vessels around the cardiac outflow tract as well as to those in the facial skin and þ þ the lymph sac.