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3 Embryology and Development
BIOL 6505 − INTRODUCTION TO FETAL MEDICINE 3. EMBRYOLOGY AND DEVELOPMENT Arlet G. Kurkchubasche, M.D. INTRODUCTION Embryology – the field of study that pertains to the developing organism/human Basic embryology –usually taught in the chronologic sequence of events. These events are the basis for understanding the congenital anomalies that we encounter in the fetus, and help explain the relationships to other organ system concerns. Below is a synopsis of some of the critical steps in embryogenesis from the anatomic rather than molecular basis. These concepts will be more intuitive and evident in conjunction with diagrams and animated sequences. This text is a synopsis of material provided in Langman’s Medical Embryology, 9th ed. First week – ovulation to fertilization to implantation Fertilization restores 1) the diploid number of chromosomes, 2) determines the chromosomal sex and 3) initiates cleavage. Cleavage of the fertilized ovum results in mitotic divisions generating blastomeres that form a 16-cell morula. The dense morula develops a central cavity and now forms the blastocyst, which restructures into 2 components. The inner cell mass forms the embryoblast and outer cell mass the trophoblast. Consequences for fetal management: Variances in cleavage, i.e. splitting of the zygote at various stages/locations - leads to monozygotic twinning with various relationships of the fetal membranes. Cleavage at later weeks will lead to conjoined twinning. Second week: the week of twos – marked by bilaminar germ disc formation. Commences with blastocyst partially embedded in endometrial stroma Trophoblast forms – 1) cytotrophoblast – mitotic cells that coalesce to form 2) syncytiotrophoblast – erodes into maternal tissues, forms lacunae which are critical to development of the uteroplacental circulation. -
Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Fetal Membrane Architecture, Aging and Inflammation in Pregnancy And
Placenta 79 (2019) 40–45 Contents lists available at ScienceDirect Placenta journal homepage: www.elsevier.com/locate/placenta Fetal membrane architecture, aging and inflammation in pregnancy and parturition T ∗ ∗∗ Ramkumar Menona, , Lauren S. Richardsona, Martha Lappasb,c, a Division of Maternal-Fetal Medicine & Perinatal Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA b Obstetrics, Nutrition and Endocrinology Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, Victoria, Australia c Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, Victoria, Australia ARTICLE INFO ABSTRACT Keywords: Preterm birth is the single major cause of infant mortality. Short and long term outcomes for infants are often Fetal membranes worse in cases of preterm premature rupture of the fetal membranes (pPROM). Thus, increased knowledge of the Structure structure characteristics of fetal membranes as well as the mechanisms of membrane rupture are essential if we Senescence are to develop effective treatment strategies to prevent pPROM. In this review, we focus on the role of in- Inflammation flammation and senescence in fetal membrane biology. 1. Introduction 2. Fetal membrane growth and microfractures Human fetal membranes (placental membranes or amniochorionic Amnion and chorion takes distinct growth trajectory upon embry- membranes) is the innermost tissue layer that forms the intrauterine ogenesis [9]. The development of amnion and chorion begins with cavity [1,2]. Fetal membranes are comprised of amnion (innermost embryogenesis although they do not participate in the formation of the layer of the intraamniotic cavity) and chorion (fetal tissue connected to embryo or fetus [10–12]. -
Infections at the Maternal–Fetal Interface: an Overview of Pathogenesis and Defence
REVIEWS Infections at the maternal–fetal interface: an overview of pathogenesis and defence Christina J. Megli 1 ✉ and Carolyn B. Coyne 2 ✉ Abstract | Infections are a major threat to human reproductive health, and infections in pregnancy can cause prematurity or stillbirth, or can be vertically transmitted to the fetus leading to congenital infection and severe disease. The acronym ‘TORCH’ (Toxoplasma gondii, other, rubella virus, cytomegalovirus, herpes simplex virus) refers to pathogens directly associated with the development of congenital disease and includes diverse bacteria, viruses and parasites. The placenta restricts vertical transmission during pregnancy and has evolved robust mechanisms of microbial defence. However, microorganisms that cause congenital disease have likely evolved diverse mechanisms to bypass these defences. In this Review, we discuss how TORCH pathogens access the intra- amniotic space and overcome the placental defences that protect against microbial vertical transmission. Infections during pregnancy can be associated with pathogen mediated, placenta mediated and/or can be devastating consequences to the pregnant mother and through inflammation induced previable delivery. developing fetus. Vertical transmission, defined as There are also outcomes of congenital infections that infection of the fetus from the maternal host, is a major do not manifest until after delivery. These can include cause of morbidity and mortality in pregnancy. In some hearing loss, developmental delays and/or blindness as cases, bacterial, viral and parasitic infections induce detailed below. dire outcomes in the fetus. The sequelae of infections Inflammation initiated by an infection of the mater in pregnancy include teratogenic effects, which cause nal host is also a known cause of preterm labour and can congenital anomalies; growth restriction, stillbirth, mis result in previable delivery or sequelae of prematurity10 carriage and neonatal death; prematurity; and maternal with lifelong consequences to the neonate. -
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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. -
Introduction to Plant Embryology Dr
Introduction to Plant embryology Dr. Pallavi J.N.L. College Khagaul Plant Embryology • Embryology is the study of structure and development of embryo, including the structure and development of male and female reproductive organs, fertilisation and similar other processes. • Father of Indian Plant empryology- Panchanan Maheshwari • Plant embryogenesis is a process that occurs after the fertilization of an ovule to produce a fully developed plant embryo. This is a pertinent stage in the plant life cycle that is followed by dormancy and germination. • The zygote produced after fertilization, must undergo various cellular divisions and differentiations to become a mature embryo. An end stage embryo has five major components including the shoot apical meristem, hypocotyl, root meristem, root cap, and cotyledons. Unlike animal embryogenesis, plant embryogenesis results in an immature form of the plant, lacking most structures like leaves, stems, and reproductive structures. • The Phanerogams (the flowering-plants) are also called spermatophytes (the seed bearing plants). These plants propagate mainly through seeds. The seed is a structure in which the embryo is enclosed. Adjacent to the embryo, foods are stored either inside the endosperm (albuminous) or in cotyledon (exalbuminous) for future use. Life cycle of flowering plants • Alternation between a dominant sporophytic generation and a highly reduced gametophytic generation. Dominant sporophytic generation is diploid and reduced gaThe normal sexual cycle (amphimixing) involves two important processes: • (i) Meiosis and • (ii) Fertilization • In meiosis also known as reduction division, a diploid sporophytic cell spore mother cell) • gets converted into four haploid gametophytic cells. (“2n” number of chromosomes becomes half i.e. “n” number of chromosome) gametophytic generation is haploid. -
Embryology BOLK’S COMPANIONS FOR‑THE STUDY of MEDICINE
Embryology BOLK’S COMPANIONS FOR‑THE STUDY OF MEDICINE EMBRYOLOGY Early development from a phenomenological point of view Guus van der Bie MD We would be interested to hear your opinion about this publication. You can let us know at http:// www.kingfishergroup.nl/ questionnaire/ About the Louis Bolk Institute The Louis Bolk Institute has conducted scientific research to further the development of organic and sustainable agriculture, nutrition, and health care since 1976. Its basic tenet is that nature is the source of knowledge about life. The Institute plays a pioneering role in its field through national and international collaboration by using experiential knowledge and by considering data as part of a greater whole. Through its groundbreaking research, the Institute seeks to contribute to a healthy future for people, animals, and the environment. For the Companions the Institute works together with the Kingfisher Foundation. Publication number: GVO 01 ISBN 90-74021-29-8 Price 10 € (excl. postage) KvK 41197208 Triodos Bank 212185764 IBAN: NL77 TRIO 0212185764 BIC code/Swift code: TRIONL 2U For credit card payment visit our website at www.louisbolk.nl/companions For further information: Louis Bolk Institute Hoofdstraat 24 NL 3972 LA Driebergen, Netherlands Tel: (++31) (0) 343 - 523860 Fax: (++31) (0) 343 - 515611 www.louisbolk.nl [email protected] Colofon: © Guus van der Bie MD, 2001, reprint 2011 Translation: Christa van Tellingen and Sherry Wildfeuer Design: Fingerprint.nl Cover painting: Leonardo da Vinci BOLK FOR THE STUDY OF MEDICINE Embryology ’S COMPANIONS Early Development from a Phenomenological Point of view Guus van der Bie MD About the author Guus van der Bie MD (1945) worked from 1967 to Education, a project of the Louis Bolk Instituut to 1976 as a lecturer at the Department of Medical produce a complement to the current biomedical Anatomy and Embryology at Utrecht State scientific approach of the human being. -
Messages from the Placentae Across Multiple Species a 50 Years
Placenta 84 (2019) 14–27 Contents lists available at ScienceDirect Placenta journal homepage: www.elsevier.com/locate/placenta Messages from the placentae across multiple species: A 50 years exploration T Hiroaki Soma Saitama Medical University, Japan ARTICLE INFO ABSTRACT Keywords: This review explores eight aspects of placentation in multiple mammalian. Gestational trophoblastic disease 1) Specialities of gestational trophoblastic disease. SUA(Single umbilical artery) 2) Clinical significance of single umbilical artery (SUA) syndrome. DIC(Disseminated intravascular coagulation) in 3) Pulmonary trophoblast embolism in pregnant chinchillas and DIC in pregnant giant panda. giant panda 4) Genetics status and placental behaviors during Japanese serow and related antelopes. Placentation in Japanese serow 5) Specific living style and placentation of the Sloth and Proboscis monkey. Hydatidiform mole in chimpanzee Placentation in different living elephant 6) Similarities of placental structures between human and great apes. Manatee and hyrax 7) Similarities of placental forms in elephants, manatees and rock hyrax with different living styles. Specific placental findings of Himalayan people 8) Specialities of placental pathology in Himalayan mountain people. Conclusions: It was taught that every mammalian species held on placental forms applied to different environ- mental life for their infants, even though their gestational lengths were different. 1. Introduction of effective chemotherapeutic agents. In 1959, I was fortunate tore- ceive an invitation from Prof. Kurt Benirschke at the Boston Lying-in Last October, Scientific American published a special issue about a Hospital. Before that, I had written to Prof. Arthur T. Hertig, Chairman baby's first organ, the placenta [1]. It is full of surprises and amazing of Pathology, Harvard Medical School, asking to study human tropho- science. -
FASD Effects of Alcohol on a Fetus
EFFECTS OF ALCOHOL ON A FETUS “Of all the substances of abuse (including cocaine, heroin, and marijuana), alcohol produces by far the most serious neurobehavioral effects in the fetus.” —Institute of Medicine Report to Congress, 19961 Prenatal exposure to alcohol can damage a fetus at any time, causing problems that persist throughout the individual’s life. There is no known safe level of alcohol use in pregnancy. WHAT IS THE SCOPE OF THE PROBLEM? identified in virtually every part of the body, including the brain, face, eyes, ears, heart, kidneys, and bones. No Alcohol is one of the most dangerous teratogens, which single mechanism can account for all the problems that are substances that can damage a developing fetus.1 Every alcohol causes. Rather, alcohol sets in motion many time a pregnant woman has a drink, her unborn child processes at different sites in the developing fetus: has one, too. Alcohol, like carbon monoxide from cigarettes, passes easily through the placenta from the • Alcohol can trigger cell death in a number of ways, mother's bloodstream into her baby's blood (See Figure causing different parts of the fetus to develop abnormally. 1)—and puts her fetus at risk of having a fetal alcohol • Alcohol can disrupt the way nerve cells develop, travel spectrum disorder (FASD). The blood alcohol level to form different parts of the brain, and function. (BAC) of the fetus becomes equal to or greater than the blood alcohol level of the mother. Because the fetus • By constricting the blood vessels, alcohol interferes with cannot break down alcohol the way an adult can, its BAC blood flow in the placenta, which hinders the delivery 2 remains high for a longer period of time. -
Epigenetics Overview Kim Boekelheide Brown University
Formative Center for the Evaluation of Environmental Impacts on Fetal Development Epigenetics Overview Kim Boekelheide Brown University I have funding from NIEHS, USEPA, and the American Chemistry Council. I am an occasional expert consultant for chemical and pharmaceutical companies, and own stock in CytoSolv, an early stage biotechnology company developing a wound healing therapeutic. Formative Center for the Evaluation of Environmental Impacts on Fetal Development Transgenerational Influences Later Life Outcomes Clinical Events and Susceptibilities • Growth Lifestyle, • Neurobehavior Nutrition & Social • Reproduction Stressors • Obesity • Cancer Developmental Exposures Developmental Environmental Chemicals Developmental Origins of Health and Disease Formative Center for the Evaluation of Environmental Impacts on Fetal Development http://embryology.med.unsw.edu.au/MolDev/epigenetic.htm http://embryology.med.unsw.edu.au/MolDev/epigenetic.htm Formative Center for the Evaluation of Environmental Impacts on Fetal Development Cartoon depicting the mechanism of miRNA transcription, processing, and regulatory activity. miRNA genes are transcribed by RNA polymerase II to form primary miRNA (pri-miRNA) molecules Greco S J , Rameshwar P PNAS 2007;104:15484-15489 ©2007 by National Academy of Sciences Formative Center for the Evaluation of Environmental Impacts on Fetal Development Formative Center for the Evaluation of Environmental Impacts on Fetal Development Female Adult Egg A active, B suppressed Imprinting Zygote Male Adult Sperm A suppressed, -
Increased Apoptosis in Chorionic Trophoblasts of Human Fetal Membranes with Labor at Term*
International Journal of Clinical Medicine, 2012, 3, 136-142 http://dx.doi.org/10.4236/ijcm.2012.32027 Published Online March 2012 (http://www.SciRP.org/journal/ijcm) Increased Apoptosis in Chorionic Trophoblasts of Human * Fetal Membranes with Labor at Term Hassan M. Harirah1#, Mostafa A. Borahay1, Wahidu Zaman1, Mahmoud S. Ahmed1, Ibrahim G. Hager2, Gary D. V. Hankins1 1The Department of Obstetrics & Gynecology, The University of Texas Medical Branch, Galveston, USA; 2The Department of Ob- stetrics & Gynecology, Zagazig University, Zagazig, Egypt. Email: #[email protected] Received December 7th, 2011; revised January 17th, 2012; accepted February 8th, 2012 ABSTRACT Objective: To determine the association of apoptosis in the layers of human fetal membranes distal to rupture site with labor at term. Study Design: Fetal membranes were collected from elective cesarean sections (n = 8) and spontaneous vaginal deliveries (n = 8) at term. The extent of apoptosis within fetal membrane layers was determined using terminal deoxynucleotidyl transferase deoxy-UTP-nick end labeling (TUNEL) assay and western blots for pro-apoptotic active caspase-3 and anti-apoptotic Bcl-2. Results: Apoptotic index in chorionic trophoblasts of membranes distal to rupture site obtained after vaginal delivery was 3-fold higher than those obtained from elective cesarean (11.57% ± 4.98% and 4.05% ± 2.4% respectively; p = 0.012). The choriodecidua layers after vaginal deliveries had higher expression of the pro-apoptotic active caspase-3 and less expression of the anti-apoptotic Bcl-2 than those obtained from elective cesar- ean sections. Conclusions: Labor at term is associated with increased apoptosis in chorionic trophoblast cells of human fetal membranes distal to rupture site. -
Folding of Embryo
❑There is progressive increase in the size of the embryonic disc due to rapid growth of cells of central part of embryonic disc and rapid growth of somites. ❑ This causes conversion of flat pear-shaped germ disc into a cylindrical embryo. ❑The head and tail ends of the disc remain relatively close together.The increased length of the disc causes it to bulge upward into the amniotic cavity. ❑With the formation of the head and tail folds, parts of the yolk sac become enclosed within the embryo. ❑ In this way, a tube lined by endoderm is formed in the embryo. This is the primitive gut, from which most of the gastrointestinal tract is derived. ❑ At first, the gut is in wide communication with the yolk sac. The part of the gut cranial to this communication is called the foregut; the part caudal to the communication is called the hindgut; while the intervening part is called the midgut . ❑The communication with the yolk sac becomes progressively narrower. As a result of these changes, the yolk sac becomes small and inconspicuous, and is now termed the definitive yolk sac (also called the umbilical vesicle). ❑The narrow channel connecting it to the gut is called the vitellointestinal duct (also called vitelline duct; yolk stalk or omphalomesenteric duct). This duct becomes elongated and eventually disappears. ❑With the formation of the cavity, the embryo (along with the amniotic cavity and yolk sac) remains attached to the trophoblast only by extraembryonic mesoderm into which the coelom does not exist. This extraembryonic mesoderm forms the connecting stalk.