Embryology of the Respiratory System
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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 -
Prospective Isolation of NKX2-1–Expressing Human Lung Progenitors Derived from Pluripotent Stem Cells
The Journal of Clinical Investigation RESEARCH ARTICLE Prospective isolation of NKX2-1–expressing human lung progenitors derived from pluripotent stem cells Finn Hawkins,1,2 Philipp Kramer,3 Anjali Jacob,1,2 Ian Driver,4 Dylan C. Thomas,1 Katherine B. McCauley,1,2 Nicholas Skvir,1 Ana M. Crane,3 Anita A. Kurmann,1,5 Anthony N. Hollenberg,5 Sinead Nguyen,1 Brandon G. Wong,6 Ahmad S. Khalil,6,7 Sarah X.L. Huang,3,8 Susan Guttentag,9 Jason R. Rock,4 John M. Shannon,10 Brian R. Davis,3 and Darrell N. Kotton1,2 2 1Center for Regenerative Medicine, and The Pulmonary Center and Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA. 3Center for Stem Cell and Regenerative Medicine, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center, Houston, Texas, USA. 4Department of Anatomy, UCSF, San Francisco, California, USA. 5Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, USA. 6Department of Biomedical Engineering and Biological Design Center, Boston University, Boston, Massachusetts, USA. 7Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, Massachusetts, USA. 8Columbia Center for Translational Immunology & Columbia Center for Human Development, Columbia University Medical Center, New York, New York, USA. 9Department of Pediatrics, Monroe Carell Jr. Children’s Hospital, Vanderbilt University, Nashville, Tennessee, USA. 10Division of Pulmonary Biology, Cincinnati Children’s Hospital, Cincinnati, Ohio, USA. It has been postulated that during human fetal development, all cells of the lung epithelium derive from embryonic, endodermal, NK2 homeobox 1–expressing (NKX2-1+) precursor cells. -
Development of the Female Reproductive System
Development of the female Reproductive System Dr. Susheela Rani Genital System •Gonads •Internal genitals •External genitals Determining sex – chronology of events •Determined Genetic sex at fertilization Gonadal sex •6th week Phenotypic sex •Differentiation of Behavioural Psyche - Preoptic and Median region Sex of Hypothalamus Genetic Sex Genetic sex of an embryo is determined at the time of fertilization, depending on whether the spermatocyte carries an X or a Y chromosome. The ‘Master’ Gene that determines Gender • SRY (Sex determining Region Y gene) • Has a testis-determining effect on the indifferent gonads. • Small gene (a single exon) • Localized on the shorter arm of the Y chromosome (Yp) • Gets expressed in the gonadal cells • Controls a whole number of further genes on the autosomes as well as on the X chromosome. • Causes development of Testes • Pseudo autosomal regions PAR1 and PAR 2 – Yellow • Heterochromatin – redundant DNA sequences – Pink • SRY – Region for Sex Determining Gene- Dark red • ZFY , Y linked Zinc Finger Protein – Orange • Spermatogenesis Genes in long arm – Azoospermia factor AZF • Telomeres – green • Centromeres - Blue It is not the number of gonosomes that is decisive for the gender, but rather the presence or absence of the Y-chromosome Aneuploidy and Euploidy of Gonosomes Karyotype Phenotypic Gonad Syndrome Fate Gender 45, XO Female Ovaries Turner’s Atrophy of Ovaries in the fetus 45, YO ------ ----- ----- Absence of X chromosome is lethal 46, XX Female Ovaries Normal Normal Development Woman 47, XXX Female -
Malignant Pleural Mesothelioma
CLINICAL PRACTICE GUIDELINE LU-009 Version 2 MALIGNANT PLEURAL MESOTHELIOMA Effective Date: December, 2012 The recommendations contained in this guideline are a consensus of the Alberta Provincial Thoracic Malignancies Tumour Team synthesis of currently accepted approaches to management, derived from a review of relevant scientific literature. Clinicians applying these guidelines should, in consultation with the patient, use independent medical judgment in the context of individual clinical circumstances to direct care. CLINICAL PRACTICE GUIDELINE LU-009 Version 2 BACKGROUND Mesothelioma is a rare asbestos-related tumour that arises from mesenchymal cells that are found in the lining of the pleural cavity (Malignant Pleural Mesothelioma; MPM) in 70 to 90 percent of cases, and the peritoneal cavity in 10 to 30 percent of cases.1, 2 Due to the long latency period between exposure and disease, which has been reported to be between 30 and 50 years, most cases of mesothelioma being diagnosed today are the result of asbestos exposure in the 1960s and 1970s.3 Although safety measures for the use of asbestos were adopted in most countries several decades ago, the incidence rates, which are highly age-specific, are still rising, and are expected to peak over the next two decades.4-6 In Canada, the number of men diagnosed with mesothelioma has been steadily increasing over the past 20 years: there were 153 cases reported in 1984 versus 344 cases reported in 2003.3 Mesothelioma is less common in women: there were 78 Canadian women diagnosed with mesothelioma in 2003.3 In the United States, the peak mesothelioma incidence occurred in the early to mid-1990s and has possibly started to decline since then. -
Nasal Cavity Trachea Right Main (Primary) Bronchus Left Main (Primary) Bronchus Nostril Oral Cavity Pharynx Larynx Right Lung
Nasal cavity Oral cavity Nostril Pharynx Larynx Trachea Left main Right main (primary) (primary) bronchus bronchus Left lung Right lung Diaphragm © 2018 Pearson Education, Inc. 1 Cribriform plate of ethmoid bone Sphenoidal sinus Frontal sinus Posterior nasal aperture Nasal cavity • Nasal conchae (superior, Nasopharynx middle, and inferior) • Pharyngeal tonsil • Nasal meatuses (superior, middle, and inferior) • Opening of pharyngotympanic • Nasal vestibule tube • Nostril • Uvula Hard palate Oropharynx • Palatine tonsil Soft palate • Lingual tonsil Tongue Laryngopharynx Hyoid bone Larynx Esophagus • Epiglottis • Thyroid cartilage Trachea • Vocal fold • Cricoid cartilage (b) Detailed anatomy of the upper respiratory tract © 2018 Pearson Education, Inc. 2 Pharynx • Nasopharynx • Oropharynx • Laryngopharynx (a) Regions of the pharynx © 2018 Pearson Education, Inc. 3 Posterior Mucosa Esophagus Submucosa Trachealis Lumen of Seromucous muscle trachea gland in submucosa Hyaline cartilage Adventitia (a) Anterior © 2018 Pearson Education, Inc. 4 Intercostal muscle Rib Parietal pleura Lung Pleural cavity Trachea Visceral pleura Thymus Apex of lung Left superior lobe Right superior lobe Oblique Horizontal fissure fissure Right middle lobe Left inferior lobe Oblique fissure Right inferior lobe Heart (in pericardial cavity of mediastinum) Diaphragm Base of lung (a) Anterior view. The lungs flank mediastinal structures laterally. © 2018 Pearson Education, Inc. 5 Posterior Vertebra Esophagus (in posterior mediastinum) Root of lung at hilum Right lung • Left main bronchus Parietal pleura • Left pulmonary artery • Left pulmonary vein Visceral pleura Pleural cavity Left lung Thoracic wall Pulmonary trunk Pericardial membranes Heart (in mediastinum) Sternum Anterior mediastinum Anterior (b) Transverse section through the thorax, viewed from above © 2018 Pearson Education, Inc. 6 Alveolar duct Alveoli Respiratory bronchioles Alveolar duct Terminal bronchiole Alveolar sac (a) Diagrammatic view of respiratory bronchioles, alveolar ducts, and alveoli © 2018 Pearson Education, Inc. -
2/2/2011 1 Development of Development of Endodermal
2/2/2011 ZOO 401- Embryology-Dr. Salah A. Martin DEVELOPMENT OF THE DIGESTIVE SYSTEM ◦ Primitive Gut Tube ◦ Proctodeum and Stomodeum ◦ Stomach Development of Endodermal Organs ◦ Duodenum ◦ Pancreas ◦ Liver and Biliary Apparatus ◦ Spleen ◦ Midgut Wednesday, February 02, 2011 DEVELOPMENT OF THE DIGESTIVE SYSTEM 2 Wednesday, February 02, 2011 Development of Ectodermal Organs 1 ZOO 401- Embryology-Dr. Salah A. Martin ZOO 401- Embryology-Dr. Salah A. Martin Primitive Gut Tube Proctodeum and Stomodeum The primitive gut tube is derived from the dorsal part of the yolk sac , which is incorporated into the body of The proctodeum (anal pit) is the primordial the embryo during folding of the embryo during the fourth week. anus , and the stomodeum is the primordial The primitive gut tube is divided into three sections. mouth . The epithelium of and the parenchyma of In both of these areas ectoderm is in direct glands associated with the digestive tract (e.g., liver and pancreas) are derived from endoderm . contact with endoderm without intervening The muscular walls of the digestive tract (lamina mesoderm, eventually leading to degeneration propria, muscularis mucosae, submucosa, muscularis of both tissue layers. Foregut, Esophagus. externa, adventitia and/or serosa) are derived from splanchnic mesoderm . The tracheoesophageal septum divides the During the solid stage of development the endoderm foregut into the esophagus and of the gut tube proliferates until the gut is a solid tube. trachea. information. A process of recanalization restores the lumen. Wednesday, February 02, 2011 Primitive Gut Tube 3 Wednesday, February 02, 2011 Proctodeum and Stomodeum 4 ZOO 401- Embryology-Dr. Salah A. -
Urinary System Intermediate Mesoderm
Urinary System Intermediate mesoderm lateral mesoderm: somite ectoderm neural NOTE: Intermediate mesoderm splanchnic groove somatic is situated between somites and lateral mesoderm (somatic and splanchnic mesoderm bordering the coelom). All mesoderm is derived from the primary mesen- intermediate mesoderm endoderm chyme that migrated through the notochord coelom (becomes urogenital ridge) primitive streak. Intermediate mesoderm (plus adjacent mesothelium lining the coelom) forms a urogenital ridge, which consists of a laterally-positioned nephrogenic cord (that forms kidneys & ureter) and a medially-positioned gonadal ridge (for ovary/testis & female/male genital tract formation). Thus urinary & genital systems have a common embryonic origin; also, they share common ducts. NOTE: Urine production essentially requires an increased capillary surface area (glomeruli), epithelial tubules to collect plasma filtrate and extract desirable constituents, and a duct system to convey urine away from the body. Kidneys Bilateraly, three kid- mesonephric duct neys develop from the neph- metanephros pronephros rogenic cord. They develop mesonephric tubules chronologically in cranial- mesonephros caudal sequence, and are designated pro—, meso—, Nephrogenic Cord (left) and meta—, respectively. cloaca The pronephros and mesonephros develop similarly: the nephrogenic cord undergoes seg- mentation, segments become tubules, tubules drain into a duct & eventually tubules disintegrate. spinal ganglion 1] Pronephros—consists of (7-8) primitive tubules and a pronephric duct that grows caudally and terminates in the cloaca. The tubules soon degenerate, but the pronephric duct persists as the neural tube mesonephric duct. (The pronephros is not functional, somite except in sheep.) notochord mesonephric NOTE tubule The mesonephros is the functional kidney for fish and am- aorta phibians. The metanephros is the functional kidney body of reptiles, birds, & mammals. -
Embryology, Comparative Anatomy, and Congenital Malformations of the Gastrointestinal Tract
Edorium J Anat Embryo 2016;3:39–50. Danowitz et al. 39 www.edoriumjournals.com/ej/ae REVIEW ARTICLE PEER REVIEWED | OPEN ACCESS Embryology, comparative anatomy, and congenital malformations of the gastrointestinal tract Melinda Danowitz, Nikos Solounias ABSTRACT Human digestive development is an essential topic for medical students and physicians, Evolutionary biology gives context to human and many common congenital abnormalities embryonic digestive organs, and demonstrates directly relate to gastrointestinal embryology. how structural adaptations can fit changing We believe this comprehensive review of environmental requirements. Comparative gastrointestinal embryology and comparative anatomy is rarely included in the medical anatomy will facilitate a better understanding of school curriculum. However, its concepts gut development, congenital abnormalities, and facilitate a deeper comprehension of anatomy adaptations to various evolutionary ecological and development by putting the morphology conditions. into an evolutionary perspective. Features of gastrointestinal development reflect the transition Keywords: Anatomy education, Digestive, Embry- from aquatic to terrestrial environments, such as ology, Gastrointestinal tract the elongation of the colon in land vertebrates, allowing for better water reabsorption. In How to cite this article addition, fishes exhibit ciliary transport in the esophagus, which facilitates particle transport in Danowitz M, Solounias N. Embryology, comparative water, whereas land mammals develop striated anatomy, and congenital malformations of the and smooth esophageal musculature and utilize gastrointestinal tract. Edorium J Anat Embryo peristaltic muscle contractions, allowing for 2016;3:39–50. better voluntary control of swallowing. The development of an extensive vitelline drainage system to the liver, which ultimately creates Article ID: 100014A04MD2016 the adult hepatic portal system allows for the evolution of complex hepatic metabolic ********* functions seen in many vertebrates today. -
Regulation of Early Lung Morphogenesis: Questions, Facts and Controversies
REVIEW 1611 Development 133, 1611-1624 (2006) doi:10.1242/dev.02310 Regulation of early lung morphogenesis: questions, facts and controversies Wellington V. Cardoso* and Jining Lü During early respiratory system development, the foregut endodermal specification, lung primordium formation, and the endoderm gives rise to the tracheal and lung cell progenitors. regulation of the initial stages of branching morphogenesis and Through branching morphogenesis, and in coordination with differentiation in the embryonic lung. We address questions such as vascular development, a tree-like structure of epithelial ‘when and how is respiratory cell fate established?’, ‘how do lung tubules forms and differentiates to produce the airways and buds form?’, ‘how are stereotypical patterns of airway branching and alveoli. Recent studies have implicated the fibroblast growth cellular diversity generated in the developing lung?’ and ‘which factor, sonic hedgehog, bone morphogenetic protein, retinoic pathways and targets are key to these processes?’. Most of what is acid and Wnt signaling pathways, and various transcription described refers to mouse lung development because of the genetic factors in regulating the initial stages of lung development. data available (Table 1). Lung vascular development and later events, However, the precise roles of these molecules and how they such as sacculation and alveoli formation, are not discussed in this interact in the developing lung is subject to debate. Here, we review (for reviews, see Pauling and Vu, 2004; Williams, -
Branching Morphogenesis of the Lung: New Molecular Insights Into an Old Problem
86 Review TRENDS in Cell Biology Vol.13 No.2 February 2003 Branching morphogenesis of the lung: new molecular insights into an old problem Pao-Tien Chuang1 and Andrew P. McMahon2 1Cardiovascular Research Institute, University of California, San Francisco, CA 94143, USA 2Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA It has been known for decades that branching morpho- This process coincides with the appearance of another genesis of the lung is mediated through reciprocal inter- endodermal derivative, the dorsal pancreatic bud pri- actions between the epithelium and its underlying mordium, whereas the liver and thyroid bud emerge one mesenchyme. In recent years, several key players, in day earlier from the ventral foregut endoderm [5]. The particular members of the major signaling pathways lung primordium is composed of two parts: the future that mediate this interaction, have been identified. Here, trachea and two endodermal buds (primary buds), which we review the genetic and molecular studies of these give rise to the left and right lobes of the distal lung. Both key components, which have provided a conceptual components are composed of an epithelial layer of endo- framework for understanding the interactions of these derm surrounded by splanchnic lateral plate mesoderm major signaling pathways in branching morphogenesis. cells. Initially the primary buds grow ventrally and The future challenge is to translate understanding of caudally, and initiate lateral branches at invariant posi- the signaling cascade into knowledge of the cellular tions, beginning around 10.5 dpc. In this way, five responses, including cell proliferation, migration and secondary buds are generated, four on the right side and differentiation, that lead to the stereotyped branching.* one on the left side, leading to the formation of four right lobes and one left lobe of the mature lung in mice. -
Embryology Dr. Azal N.Al-Nusear Respiratory System 1-Upper
Embryology Dr. Azal N.Al-Nusear Respiratory System 1-Upper Respiratory System: The upper respiratory system consists of the nose, nasopharynx, and oropharynx. 2-Lower Respiratory system: The lower respiratory system consists of the larynx, trachea, bronchi, and lungs. The first sign of development is the formation of the respiratory diverticulum in the ventral wall of the primitive foregut during week 4. The distal end of the respiratory diverticulum enlarges to form the lung bud. The lung bud divides into two bronchial buds that branch into the primary, secondary, tertiary, and subsegmental bronchi. The respiratory diverticulum initially is in open communication with the foregut, but eventually they become separated by mesoderm (tracheoesophageal folds). When the tracheoesophageal folds fuse in the midline to form the tracheoesophageal septum, the foregut is divided into the trachea ventrally and esophagus dorsally. RD: respiratory diverticulum F: foregut. VM: visceral mesoderm. TEF : tracheoesophageal folds the trachea (T) and esophagus (E). B = bronchial buds. LL = left lung; L = right lung; Development of Individual Parts of the Respiratory System Larynx The larynx develops from the cranial part of laryngotracheal diverticulum. The opening of the respiratory diverticulum into the foregut becomes the laryngeal orifice. The mesenchyme (of fourth and sixth pharyngeal arches) surrounding the laryngeal orifice proliferates. As a result, the slit-like laryngeal orifice becomes T shaped. Subsequently laryngeal orifice acquires a characteristic adult shape. The lining epithelium of larynx develops from endoderm of this diverticulum. At first the endodermal cells proliferate and completely obliterate lumen of larynx. Later the cells breakdown and recanalization of larynx take place.