Development of the Genital System Development of the Gonads
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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 -
Male Reproductive System Sexual Reproduction Requires Two Types Of
Male Reproductive system Sexual reproduction requires two types of gametes or sex cells. In the male these cells are the spermatozoa and in the female they are the ova. The reproductive systems are unique in three respects 1. They are specialized in perpetuating the species and passing genetic information. 2. The anatomy and physiology between the male and female reproductive systems are different. 3. They exhibit latent development under hormonal control. The structures of the male reproductive system can be divided into three categories. 1. Primary sex organs - the gonads (testes). These produce sperm and sex hormones. 2. Secondary sex organs - the structures necessary for caring for and transportation of the sperm. A. Sperm transporting ducts 1. epididymus 2. ductus deferens 3. ejaculatory ducts 4. urethra B. Accessory glands 1. seminal vesicle 2. prostate gland 3. bulbourethral (Cowper's) glands C. Copulatory organ - penis. Also includes the scrotum (the skin enclosing the testes) 3. Secondary sex characteristics - These are not reproductively necessary, but are considered sexual attractants. They include things such as body hair, body physique, and voice pitch. Sexual determination - Sex is determined at the time of conception. As we will see, all ova have an x chromosome and sperm are 50:50 X and Y. If an ova is fertilized by an x sperm then we have a female. If an ova is fertilized by a Y sperm then we have a male. Sometimes we see more than one X in an ovum. As long as there is a Y chromosome we will have a male. ie. XXXY = male. -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal. -
Comparative Gene Expression Analysis of Genital Tubercle Development Reveals a Putative Appendicular Wnt7 Network for the Epidermal Differentiation
Developmental Biology 344 (2010) 1071–1087 Contents lists available at ScienceDirect Developmental Biology journal homepage: www.elsevier.com/developmentalbiology Genomes & Developmental Control Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation Han Sheng Chiu a, John C. Szucsik b, Kylie M. Georgas a, Julia L. Jones c, Bree A. Rumballe a, Dave Tang a, Sean M. Grimmond a, Alfor G. Lewis b, Bruce J. Aronow b,c, James L. Lessard b, Melissa H. Little a,⁎ a Institute for Molecular Bioscience, The University of Queensland, St. Lucia 4072, Australia b Division of Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229, USA c Division of Biomedical Informatics, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229, USA article info abstract Article history: Here we describe the first detailed catalog of gene expression in the developing lower urinary tract (LUT), Received for publication 30 November 2009 including epithelial and mesenchymal portions of the developing bladder, urogenital sinus, urethra, and Revised 23 April 2010 genital tubercle (GT) at E13 and E14. Top compartment-specific genes implicated by the microarray data Accepted 15 May 2010 were validated using whole-mount in situ hybridization (ISH) over the entire LUT. To demonstrate the Available online 24 May 2010 potential of this resource to implicate developmentally critical features, we focused on gene expression Keywords: patterns and pathways in the sexually indeterminate, androgen-independent GT. GT expression patterns Genital tubercle development reinforced the proposed similarities between development of GT, limb, and craniofacial prominences. Lower urinary tract development Comparison of spatial expression patterns predicted a network of Wnt7a-associated GT-enriched epithelial Gene expression genes, including Gjb2, Dsc3, Krt5, and Sostdc1. -
Pocket Atlas of Human Anatomy 4Th Edition
I Pocket Atlas of Human Anatomy 4th edition Feneis, Pocket Atlas of Human Anatomy © 2000 Thieme All rights reserved. Usage subject to terms and conditions of license. III Pocket Atlas of Human Anatomy Based on the International Nomenclature Heinz Feneis Wolfgang Dauber Professor Professor Formerly Institute of Anatomy Institute of Anatomy University of Tübingen University of Tübingen Tübingen, Germany Tübingen, Germany Fourth edition, fully revised 800 illustrations by Gerhard Spitzer Thieme Stuttgart · New York 2000 Feneis, Pocket Atlas of Human Anatomy © 2000 Thieme All rights reserved. Usage subject to terms and conditions of license. IV Library of Congress Cataloging-in-Publication Data is available from the publisher. 1st German edition 1967 2nd Japanese edition 1983 7th German edition 1993 2nd German edition 1970 1st Dutch edition 1984 2nd Dutch edition 1993 1st Italian edition 1970 2nd Swedish edition 1984 2nd Greek edition 1994 3rd German edition 1972 2nd English edition 1985 3rd English edition 1994 1st Polish edition 1973 2nd Polish edition 1986 3rd Spanish edition 1994 4th German edition 1974 1st French edition 1986 3rd Danish edition 1995 1st Spanish edition 1974 2nd Polish edition 1986 1st Russian edition 1996 1st Japanese edition 1974 6th German edition 1988 2nd Czech edition 1996 1st Portuguese edition 1976 2nd Italian edition 1989 3rd Swedish edition 1996 1st English edition 1976 2nd Spanish edition 1989 2nd Turkish edition 1997 1st Danish edition 1977 1st Turkish edition 1990 8th German edition 1998 1st Swedish edition 1979 1st Greek edition 1991 1st Indonesian edition 1998 1st Czech edition 1981 1st Chinese edition 1991 1st Basque edition 1998 5th German edition 1982 1st Icelandic edition 1992 3rd Dutch edtion 1999 2nd Danish edition 1983 3rd Polish edition 1992 4th Spanish edition 2000 This book is an authorized and revised translation of the 8th German edition published and copy- righted 1998 by Georg Thieme Verlag, Stuttgart, Germany. -
MR Imaging of Vaginal Morphology, Paravaginal Attachments and Ligaments
MR imaging of vaginal morph:ingynious 05/06/15 10:09 Pagina 53 Original article MR imaging of vaginal morphology, paravaginal attachments and ligaments. Normal features VITTORIO PILONI Iniziativa Medica, Diagnostic Imaging Centre, Monselice (Padova), Italy Abstract: Aim: To define the MR appearance of the intact vaginal and paravaginal anatomy. Method: the pelvic MR examinations achieved with external coil of 25 nulliparous women (group A), mean age 31.3 range 28-35 years without pelvic floor dysfunctions, were compared with those of 8 women who had cesarean delivery (group B), mean age 34.1 range 31-40 years, for evidence of (a) vaginal morphology, length and axis inclination; (b) perineal body’s position with respect to the hymen plane; and (c) visibility of paravaginal attachments and lig- aments. Results: in both groups, axial MR images showed that the upper vagina had an horizontal, linear shape in over 91%; the middle vagi- na an H-shape or W-shape in 74% and 26%, respectively; and the lower vagina a U-shape in 82% of cases. Vaginal length, axis inclination and distance of perineal body to the hymen were not significantly different between the two groups (mean ± SD 77.3 ± 3.2 mm vs 74.3 ± 5.2 mm; 70.1 ± 4.8 degrees vs 74.04 ± 1.6 degrees; and +3.2 ± 2.4 mm vs + 2.4 ± 1.8 mm, in group A and B, respectively, P > 0.05). Overall, the lower third vaginal morphology was the less easily identifiable structure (visibility score, 2); the uterosacral ligaments and the parau- rethral ligaments were the most frequently depicted attachments (visibility score, 3 and 4, respectively); the distance of the perineal body to the hymen was the most consistent reference landmark (mean +3 mm, range -2 to + 5 mm, visibility score 4). -
Mechanisms of Gonadal Morphogenesis Are Not Conserved Between Chick and Mouse ⁎ Ryohei Sekido , Robin Lovell-Badge
Developmental Biology 302 (2007) 132–142 www.elsevier.com/locate/ydbio Mechanisms of gonadal morphogenesis are not conserved between chick and mouse ⁎ Ryohei Sekido , Robin Lovell-Badge Division of Developmental Genetics, MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK Received for publication 3 June 2006; revised 16 August 2006; accepted 5 September 2006 Available online 9 September 2006 Abstract To understand mechanisms of sex determination, it is important to know the lineage relationships of cells comprising the gonads. For example, in mice, the Y-linked gene Sry triggers differentiation of Sertoli cells from a cell population originating in the coelomic epithelium overlying the nascent gonad that also gives rise to uncharacterised interstitial cells. In contrast, little is known about origins of somatic cell types in the chick testis, where there is no Sry gene and sex determination depends on a ZZ male/ZW female mechanism. To investigate this, we performed fate mapping experiments in ovo, labelling at indifferent stages the coelomic epithelium by electroporation with a lacZ reporter gene and the underlying nephrogenous (or mesonephric) mesenchyme with chemical dyes. After sex differentiation, LacZ-positive cells were exclusively outside testis cords and were 3βHSD-negative, indicating that the coelomic epithelium contributes only to non-steroidogenic interstitial cells. However, we detected dye-labelled cells both inside and outside the cords. The former were AMH-positive while some of the latter were 3βHSD- positive, showing that nephrogenous mesenchyme contributes to both Sertoli cells and steroidogenic cells. This is the first demonstration via lineage analysis that steroidogenic cells originate from nephrogenous mesenchyme, but the revelation that Sertoli cells have different origins between chick and mouse suggests that, during evolution, mechanisms of gonad morphogenesis may diverge alongside those of sex determination. -
Cranial Cavitry
Embryology Endo, Energy, and Repro 2017-2018 EMBRYOLOGY OF THE REPRODUCTIVE SYSTEM Janine Prange-Kiel, Ph.D. Office: L1.106, Phone: 83117 Email: [email protected] LEARNING OBJECTIVES: • Name the structures in kidney development that contribute to the development of the reproductive organs. • Predict how the presence or absence of the Y chromosome and the expression of the SRY gene would influence the development of the gonads. • Predict how the presence or absence of testosterone, dihydrotestosterone, and anit- Mullerian hormone would influence the development of the genital ducts and indifferent primordia of the external genitalia. I. Introduction In general, the function of the genital (reproductive) system in males and females is the formation, nurture, and transport of germ cells. In females, an additional function is to provide the proper milieu for the fetal development after conception. Like the urinary system, the genital system derives from intermediate mesoderm. The development of these two systems is tightly interwoven as structures that develop as parts of the urinary system gain function in the genital system. In the adult, the sexual organs differ between males and females. The early genital system, however, is similar in both sexes, and the sexual differentiation of this initially indifferent, bipotential system starts only in the seventh week of embryonic development. The details on how sexual differentiation is determined will be discussed below, but it is worth mentioning here that irregularities in this process result in disorders of sexual differentiation (DSDs). DSDs occur in approximately 1 in 4,500 live births and will be discussed in a separate lecture. -
Tests Spring 2012
Tests spring 2013 Test 1 Oral cavity 1. Vestibulum oris does not communicate with proper oral cavity through: :r1 oral part of pharynx :r2 tremata :r3 space behind last molar :r4 space when tooth is missing :r5 communicates through all mentioned ways -- 2. Into vestibule of oral cavity opens out: :r1 caruncula sublingualis :r2 papilla parotidea :r3 ductus nasolacrimalis :r4 plica sublingualis :r5 none of mentioned answers is correct -- 3. The underlay of lips is: :r1 m. labialis :r2 m. orbicularis oculi :r3 m. orbicularis oris :r4 m. buccalis :r5 none of mentioned answers is correct -- 4. The upper lip is partially connected with alveolar process using: :r1 lig. labii superioris :r2 m. platysma :r3 frenulum labii superioris :r4 plica labii superioris :r5 none of mentioned answers is correct -- 5. Cheek is not made up of: :r1 skin :r2 adipose body :r3 muscular layer :r4 adventitia :r5 none of mentioned answers is correct -- 6. Parotid duct passes through: :r1 m. masseter :r2 m. buccinator :r3 m. orbicularis oris :r4 m. pterygoideus lateralis :r5 none of mentioned answers is correct -- 7. The underlay of hard palate is not: :r1 praemaxilla :r2 vomer :r3 processus palatinus maxillae :r4 lamina horizontalis ossis palatini :r5 all mentioned bones form the underlay of hard palate -- 8. Which statement describing mucosa of hard palate is not correct: :r1 it contains big amount of submucosal connective tissue :r2 it is covered by columnar epithelium :r3 firmly grows together with periosteum :r4 it is almost not movable against the bottom :r5 it contains glandulae palatinae -- 9. Mark the true statement describing the palate: :r1 there is papilla incisiva positioned there :r2 mucosa contains glandulae palatinae :r3 there are plicae palatinae transversae positioned there :r4 the basis of soft palate is made by fibrous aponeurosis palatina :r5 all mentioned statements are correct -- 10. -
The Derivatives of Three-Layered Embryo (Germ Layers)
HUMANHUMAN EMBRYOLOGYEMBRYOLOGY Department of Histology and Embryology Jilin University ChapterChapter 22 GeneralGeneral EmbryologyEmbryology FourthFourth week:week: TheThe derivativesderivatives ofof trilaminartrilaminar germgerm discdisc Dorsal side of the germ disc. At the beginning of the third week of development, the ectodermal germ layer has the shape of a disc that is broader in the cephalic than the caudal region. Cross section shows formation of trilaminar germ disc Primitive pit Drawing of a sagittal section through a 17-day embryo. The most cranial portion of the definitive notochord has formed. ectoderm Schematic view showing the definitive notochord. horizon =ectoderm hillside fields =neural plate mountain peaks =neural folds Cave sinks into mountain =neural tube valley =neural groove 7.1 Derivatives of the Ectodermal Germ Layer 1) Formation of neural tube Notochord induces the overlying ectoderm to thicken and form the neural plate. Cross section Animation of formation of neural plate When notochord is forming, primitive streak is shorten. At meanwhile, neural plate is induced to form cephalic to caudal end, following formation of notochord. By the end of 3rd week, neural folds and neural groove are formed. Neural folds fuse in the midline, beginning in cervical region and Cross section proceeding cranially and caudally. Neural tube is formed & invade into the embryo body. A. Dorsal view of a human embryo at approximately day 22. B. Dorsal view of a human embryo at approximately day 23. The nervous system is in connection with the amniotic cavity through the cranial and caudal neuropores. Cranial/anterior neuropore Neural fold heart Neural groove endoderm caudal/posterior neuropore A. -
ANA214: Systemic Embryology
ANA214: Systemic Embryology ISHOLA, Azeez Olakune [email protected] Anatomy Department, College of Medicine and Health Sciences Outline • Organogenesis foundation • Urogenital system • Respiratory System • Kidney • Larynx • Ureter • Trachea & Bronchi • Urinary bladder • Lungs • Male urethra • Female urethra • Cardiovascular System • Prostate • Heart • Uterus and uterine tubes • Blood vessels • Vagina • Fetal Circulation • External genitalia • Changes in Circulation at Birth • Testes • Gastrointestinal System • Ovary • Mouth • Nervous System • Pharynx • Neurulation • GI Tract • Neural crests • Liver, Spleen, Pancreas Segmentation of Mesoderm • Start by 17th day • Under the influence of notochord • Cells close to midline proliferate – PARAXIAL MESODERM • Lateral cells remain thin – LATERAL PLATE MESODERM • Somatic/Parietal mesoderm – close to amnion • Visceral/Splanchnic mesoderm – close to yolk sac • Intermediate mesoderm connects paraxial and lateral mesoderm Paraxial Mesoderm • Paraxial mesoderm organized into segments – SOMITOMERES • Occurs in craniocaudal sequence and start from occipital region • 1st developed by day 20 (3 pairs per day) – 5th week • Gives axial skeleton Intermediate Mesoderm • Differentiate into Urogenital structures • Pronephros, mesonephros Lateral Plate Mesoderm • Parietal mesoderm + ectoderm = lateral body wall folds • Dermis of skin • Bones + CT of limb + sternum • Visceral Mesoderm + endoderm = wall of gut tube • Parietal mesoderm surrounding cavity = pleura, peritoneal and pericardial cavity • Blood &