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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. -
Animal Form & Function
Animals Animal Form & Function By far, most diversity of bauplane (body forms). And most variations within bauplane. Animals are Animated “ANIMAL” ≠ MAMMAL — Fascinating Behaviors Animal Cells • Eukaryotic • No cell wall No plastids No central vacuole • Multicellular: – extensive specialization & differentiation – unique cell-cell junctions Heyer 1 Animals Animals Blastulation & Gastrulation • Motile • Early embryonic development in animals 3 In most animals, cleavage results in the formation of a multicellular stage called a 1 The zygote of an animal • Highly differentiated blastula. The blastula of many animals is a undergoes a succession of mitotic tissues cell divisions called cleavage. hollow ball of cells. Blastocoel • Intercellular junctions Cleavage Cleavage – tissue-specific cadherins 6 The endoderm of the archenteron develops into Eight-cell stage Blastula Cross section Zygote • Extracellular protein the the animal’s of blastula fibers digestive tract. Blastocoel Endoderm – collagen 5 The blind pouch formed by gastrulation, called Ectoderm • Diploid life cycle the archenteron, opens to the outside Gastrula Gastrulation via the blastopore. Blastopore 4 Most animals also undergo gastrulation, a • Blastula/gastrula rearrangement of the embryo in which one end of the embryo folds inward, expands, and eventually fills the embryo blastocoel, producing layers of embryonic tissues: the Figure 32.2 ectoderm (outer layer) and the endoderm (inner layer). Primary embryonic germ layers Primary embryonic germ layers • Diploblastic: two germ -
Stages of Embryonic Development of the Zebrafish
DEVELOPMENTAL DYNAMICS 2032553’10 (1995) Stages of Embryonic Development of the Zebrafish CHARLES B. KIMMEL, WILLIAM W. BALLARD, SETH R. KIMMEL, BONNIE ULLMANN, AND THOMAS F. SCHILLING Institute of Neuroscience, University of Oregon, Eugene, Oregon 97403-1254 (C.B.K., S.R.K., B.U., T.F.S.); Department of Biology, Dartmouth College, Hanover, NH 03755 (W.W.B.) ABSTRACT We describe a series of stages for Segmentation Period (10-24 h) 274 development of the embryo of the zebrafish, Danio (Brachydanio) rerio. We define seven broad peri- Pharyngula Period (24-48 h) 285 ods of embryogenesis-the zygote, cleavage, blas- Hatching Period (48-72 h) 298 tula, gastrula, segmentation, pharyngula, and hatching periods. These divisions highlight the Early Larval Period 303 changing spectrum of major developmental pro- Acknowledgments 303 cesses that occur during the first 3 days after fer- tilization, and we review some of what is known Glossary 303 about morphogenesis and other significant events that occur during each of the periods. Stages sub- References 309 divide the periods. Stages are named, not num- INTRODUCTION bered as in most other series, providing for flexi- A staging series is a tool that provides accuracy in bility and continued evolution of the staging series developmental studies. This is because different em- as we learn more about development in this spe- bryos, even together within a single clutch, develop at cies. The stages, and their names, are based on slightly different rates. We have seen asynchrony ap- morphological features, generally readily identi- pearing in the development of zebrafish, Danio fied by examination of the live embryo with the (Brachydanio) rerio, embryos fertilized simultaneously dissecting stereomicroscope. -
Developmental Rate and Behavior of Early Life Stages of Bighead Carp and Silver Carp
Developmental Rate and Behavior of Early Life Stages of Bighead Carp and Silver Carp Scientific Investigations Report 2011–5076 U.S. Department of the Interior U.S. Geological Survey Cover images. Left to right (top) silver carp embryo at morula stage, silver carp embryo at olfactory placode stage, silver carp embryo at otolith appearance stage, (bottom) silver carp larvae at gill filament stage, silver carp larvae at one-chamber gas bladder stage. Developmental Rate and Behavior of Early Life Stages of Bighead Carp and Silver Carp By Duane C. Chapman and Amy E. George Scientific Investigations Report 2011–5076 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2011 For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment, visit http://www.usgs.gov or call 1–888–ASK–USGS. For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod To order this and other USGS information products, visit http://store.usgs.gov Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted materials contained within this report. Suggested citation: Chapman, D.C., George, A.E., 2011, Developmental rate and behavior of early life stages of bighead carp and silver carp: U.S. -
Vertebrate Embryonic Cleavage Pattern Determination
Chapter 4 Vertebrate Embryonic Cleavage Pattern Determination Andrew Hasley, Shawn Chavez, Michael Danilchik, Martin Wühr, and Francisco Pelegri Abstract The pattern of the earliest cell divisions in a vertebrate embryo lays the groundwork for later developmental events such as gastrulation, organogenesis, and overall body plan establishment. Understanding these early cleavage patterns and the mechanisms that create them is thus crucial for the study of vertebrate develop- ment. This chapter describes the early cleavage stages for species representing ray- finned fish, amphibians, birds, reptiles, mammals, and proto-vertebrate ascidians and summarizes current understanding of the mechanisms that govern these pat- terns. The nearly universal influence of cell shape on orientation and positioning of spindles and cleavage furrows and the mechanisms that mediate this influence are discussed. We discuss in particular models of aster and spindle centering and orien- tation in large embryonic blastomeres that rely on asymmetric internal pulling forces generated by the cleavage furrow for the previous cell cycle. Also explored are mechanisms that integrate cell division given the limited supply of cellular building blocks in the egg and several-fold changes of cell size during early devel- opment, as well as cytoskeletal specializations specific to early blastomeres A. Hasley • F. Pelegri (*) Laboratory of Genetics, University of Wisconsin—Madison, Genetics/Biotech Addition, Room 2424, 425-G Henry Mall, Madison, WI 53706, USA e-mail: [email protected] S. Chavez Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Department of Physiology & Pharmacology, Oregon Heath & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Department of Obstetrics & Gynecology, Oregon Heath & Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA M. -
From Cell Death to Embryo Arrest: Mathematical Models of Human Preimplantation Embryo Development
From cell death to embryo arrest: Mathematical models of human preimplantation embryo development K. Hardy*†‡, S. Spanos*, D. Becker†§, P. Iannelli†¶, R. M. L. Winston*, and J. Stark†¶ *Department of Reproductive Science and Medicine, Imperial College School of Medicine, Hammersmith Hospital, Du Cane Road, London W12 0NN, United Kingdom; §Department of Anatomy and Developmental Biology, ¶Centre for Nonlinear Dynamics and Its Applications, and †CoMPLEX (Centre for Mathematics and Physics in the Life Sciences and Experimental Biology), University College London, Gower Street, London WC1E 6BT, United Kingdom Communicated by Paul Nurse, Imperial Cancer Research Fund, London, United Kingdom, October 18, 2000 (received for review March 23, 2000) Human preimplantation embryos exhibit high levels of apoptotic generations during which individual cells can divide or die. The cells and high rates of developmental arrest during the first week relationship between the rate of cell death for individual cells in vitro. The relation between the two is unclear and difficult to and the data in Fig. 2 is therefore complex, precluding the direct determine by conventional experimental approaches, partly be- use of standard statistical tests. Instead, we construct a mathe- cause of limited numbers of embryos. We apply a mixture of matical model of the cell division and cell death process that experiment and mathematical modeling to show that observed allows us to relate parameters such as individual cell death rates levels of cell death can be reconciled with the high levels of embryo to global outcomes, such as the distribution of live and dead cell arrest seen in the human only if the developmental competence of numbers or the arrest or survival of the whole embryo. -
Human Anatomy Bio 11 Embryology “Chapter 3”
Human Anatomy Bio 11 Embryology “chapter 3” Stages of development 1. “Pre-” really early embryonic period: fertilization (egg + sperm) forms the zygote gastrulation [~ first 3 weeks] 2. Embryonic period: neurulation organ formation [~ weeks 3-8] 3. Fetal period: growth and maturation [week 8 – birth ~ 40 weeks] Human life cycle MEIOSIS • compare to mitosis • disjunction & non-disjunction – aneuploidy e.g. Down syndrome = trisomy 21 • visit http://www.ivc.edu/faculty/kschmeidler/Pages /sc-mitosis-meiosis.pdf • and/or http://www.ivc.edu/faculty/kschmeidler/Pages /HumGen/mit-meiosis.pdf GAMETOGENESIS We will discuss, a bit, at the end of the semester. For now, suffice to say that mature males produce sperm and mature females produce ova (ovum; egg) all of which are gametes Gametes are haploid which means that each gamete contains half the full portion of DNA, compared to somatic cells = all the rest of our cells Fertilization restores the diploid state. Early embryonic stages blastocyst (blastula) 6 days of human embryo development http://www.sisuhospital.org/FET.php human early embryo development https://opentextbc.ca/anatomyandphysiology/chapter/28- 2-embryonic-development/ https://embryology.med.unsw.edu.au/embryology/images/thumb/d/dd/Model_human_blastocyst_development.jpg/600px-Model_human_blastocyst_development.jpg Good Sites To Visit • Schmeidler: http://www.ivc.edu/faculty/kschmeidler/Pages /sc_EMBRY-DEV.pdf • https://embryology.med.unsw.edu.au/embryol ogy/index.php/Week_1 • https://opentextbc.ca/anatomyandphysiology/c hapter/28-2-embryonic-development/ -
Cleavage: Types and Patterns Fertilization …………..Cleavage
Cleavage: Types and Patterns Fertilization …………..Cleavage • The transition from fertilization to cleavage is caused by the activation of mitosis promoting factor (MPF). Cleavage • Cleavage, a series of mitotic divisions whereby the enormous volume of egg cytoplasm is divided into numerous smaller, nucleated cells. • These cleavage-stage cells are called blastomeres. • In most species the rate of cell division and the placement of the blastomeres with respect to one another is completely under the control of the proteins and mRNAs stored in the oocyte by the mother. • During cleavage, however, cytoplasmic volume does not increase. Rather, the enormous volume of zygote cytoplasm is divided into increasingly smaller cells. • One consequence of this rapid cell division is that the ratio of cytoplasmic to nuclear volume gets increasingly smaller as cleavage progresses. • This decrease in the cytoplasmic to nuclear volume ratio is crucial in timing the activation of certain genes. • For example, in the frog Xenopus laevis, transcription of new messages is not activated until after 12 divisions. At that time, the rate of cleavage decreases, the blastomeres become motile, and nuclear genes begin to be transcribed. This stage is called the mid- blastula transition. • Thus, cleavage begins soon after fertilization and ends shortly after the stage when the embryo achieves a new balance between nucleus and cytoplasm. Cleavage Embryonic development Cleavage 2 • Division of first cell to many within ball of same volume (morula) is followed by hollowing -
Animal Development Bio 1413: General Zoology Laboratory Ziser, 2008 All Living Organisms Exhibit Some Form of Growth and Development
Animal Development Bio 1413: General Zoology Laboratory Ziser, 2008 All living organisms exhibit some form of growth and development. Members of the animal kingdom have the most complex developmental cycle of any living organism. The sequence of discrete, recognizable stages that these organism pass through as they develop from the formation of a zygote (the fertilized egg) to the sexually mature adult are referred to as its developmental cycle.Animal development can be subdivided into several sequential processes: gametogenesis, fertilization, embryonic development and post embryonic development. Embryonic development includes the processes of growth, determination, differentiation and morphogenesis. 1. Gametes. The gametes are produced by the process of meiosis which differs from mitosis in that only one of each chromosome ends up in the cells after division. The male gamete, the sperm, is small and almost always flagellated. The female gamete us usually large since it contains yolk, and spherical. slides: sperm smear starfish unfertilized eggs Activity Be able to distinguish between sperm and eggs and to find the following structures on slides and illustrations: for sperm identify: head, middle piece, tail (flagellum) for egg identify: cell membrane, nucleus, nucleolus 2. Fertilization. At fertilization only a single sperm penetrates and adds its chromosomes to those in the egg. The fertilized egg then has a pair of each chromosomes, one each from the male parent and the other of each from the female parent. To prevent additional sperm from penetrating the egg a fertilization cone is produced to produce the original sperm into the egg quickly. Then a fertilization membrane expands around the egg and pushes away and “locks out” other sperm cells. -
Development Development
DEVELOPMENT DEVELOPMENT • Prenatal –Before birth • Postnatal development- After birth • PRENATAL DEVELOPMENT – 1. Embryonic development – Up to 8 weeks after fertilization. Devided into 23 arbitrarory stages called as Carnegie Stages Pre implantation development Post implantation development 2.Foetal development 8 weeks onwards after fertilization Cleavage ( post fertilization) • process of subdivision of ovum into smaller cells called cleavage. • process of repeated mitotic divisions of zygote occur with in zonapellucida, • these cells are known as blastomeres, • first cleavage division occur around 24 hrs after fertilization, • during 8 cell stage compaction of cells occur within the cells flatten & increase their intercellular contact , • Cleavage proceed to 16 celled stage --- MORULA, • All cells of approximately same size, • At 16 cells stage cells polarity is determuned to form outer trophoectoderm & inner cell mass, • inner cell mass give rise to embryo in future, while outer cell mass is destined to form the fetal membranes including placenta • the inner cell mass also called embryoblast , • cells of trophoblast help to provide nutrition to embryo, blastocyst • some fluid now passes into morula from uterine cavity , & partially separate the cells of inner cell mass from trophoblast. • as quantity of fluid increases the morula acquires shape of a cyst,the cells of trophoblast flattens out & inner cell mass gets attach to one side only, • the morula now is called blastocyst ,cavity is called blastocoele. • site where blastocyst is attach to inner cell mass is calld embryonic or animal pole , while opposite site is aembryonic pole. Zona pellucida( function) • trophoblast has property of being able to stick to uterine ( or other) epithelium & its cells have capacity to eat up other cells( property of invading) • thus as embryo is travelling down the uterine tube & uppermost part of uterine cavity , it is prevented from sticking to epithelium by a zona pellucida. -
Early Embryonic Development Till Gastrulation (Humans)
Gargi College Subject: Comparative Anatomy and Developmental Biology Class: Life Sciences 2 SEM Teacher: Dr Swati Bajaj Date: 17/3/2020 Time: 2:00 pm to 3:00 pm EARLY EMBRYONIC DEVELOPMENT TILL GASTRULATION (HUMANS) CLEAVAGE: Cleavage in mammalian eggs are among the slowest in the animal kingdom, taking place some 12-24 hours apart. The first cleavage occurs along the journey of the embryo from oviduct toward the uterus. Several features distinguish mammalian cleavage: 1. Rotational cleavage: the first cleavage is normal meridional division; however, in the second cleavage, one of the two blastomeres divides meridionally and the other divides equatorially. 2. Mammalian blastomeres do not all divide at the same time. Thus the embryo frequently contains odd numbers of cells. 3. The mammalian genome is activated during early cleavage and zygotically transcribed proteins are necessary for cleavage and development. (In humans, the zygotic genes are activated around 8 cell stage) 4. Compaction: Until the eight-cell stage, they form a loosely arranged clump. Following the third cleavage, cell adhesion proteins such as E-cadherin become expressed, and the blastomeres huddle together and form a compact ball of cells. Blatocyst: The descendents of the large group of external cells of Morula become trophoblast (trophoblast produce no embryonic structure but rather form tissues of chorion, extraembryonic membrane and portion of placenta) whereas the small group internal cells give rise to Inner Cell mass (ICM), (which will give rise to embryo proper). During the process of cavitation, the trophoblast cells secrete fluid into the Morula to create blastocoel. As the blastocoel expands, the inner cell mass become positioned on one side of the ring of trophoblast cells, resulting in the distinctive mammalian blastocyst. -
New Insights Into Human Early Embryo Development: a Particular Theoretical Study
14 International Journal of Modern Anthropology Int. J. Mod. Anthrop. (2018) Vol: 2, Issue No: 11, pp: 14 - 46 Available online at: www.ata.org.tn ; DOI: http://dx.doi.org/10.4314/ijma.v2i11.1 Original Synthesis Article New insights into human early embryo development: a particular theoretical study Hassen Chaabani Laboratory of Human Genetics and Anthropology, Faculty of Pharmacy, University of Monastir, 5000 Monastir, Tunisia. E.mail: [email protected] (Received 18 January 2018; Accepted 5 Mars 2018; Published 5 May 2018) Abstract – The experimental research on the subject of human early embryo development has been remained insufficient because of ethical norms and legal constraints. In this context, the carrying out of theoretical studies could speed up the slow knowledge progression on this subject. Thus, I present here a particular model of theoretical study based on a synthesis of selected published experimental results combined with what has been provided from my interpretation of scientific signs masked in some Qur‟an verses. In the obtained detailed scenario, I consider that the third cleavage, resulting in 8 blastomeres, is coupled to a particular rearrangement in which 2 daughter cells seem move down and 2 others move up; while the 4 remaining cells seem stay at their initial position (I called them “4 HI cells”). Nevertheless, I consider that the fourth cleavage, resulting in 16 blastomeres, is coupled to a rearrangement that gives the impression of a harmonious descent: in fact, one of each two daughter cells seems pushed down. This descent materializes a morula top–bottom axis, which will go to coincide with the embryo-abembryo axis of the blastocyst.