Blastulation, Implantation, Decidua
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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. -
The Rotated Hypoblast of the Chicken Embryo Does Not Initiate an Ectopic Axis in the Epiblast
Proc. Natl. Acad. Sci. USA Vol. 92, pp. 10733-10737, November 1995 Developmental Biology The rotated hypoblast of the chicken embryo does not initiate an ectopic axis in the epiblast ODED KHANER Department of Cell and Animal Biology, The Hebrew University, Jerusalem, Israel 91904 Communicated by John Gerhart, University of California, Berkeley, CA, July 14, 1995 ABSTRACT In the amniotes, two unique layers of cells, of the hypoblast and that the orientation of the streak and axis the epiblast and the hypoblast, constitute the embryo at the can be predicted from the polarity of the stage XIII epiblast. blastula stage. All the tissues of the adult will derive from the Still it was thought that the polarity of the epiblast is sufficient epiblast, whereas hypoblast cells will form extraembryonic for axial development in experimental situations, although in yolk sac endoderm. During gastrulation, the endoderm and normal development the polarity of the hypoblast is dominant the mesoderm of the embryo arise from the primitive streak, (5, 6). These reports (1-3, 5, 6), taken together, would imply which is an epiblast structure through which cells enter the that cells of the hypoblast not only have the ability to change interior. Previous investigations by others have led to the the fate of competent cells in the epiblast to initiate an ectopic conclusion that the avian hypoblast, when rotated with regard axis, but also have the ability to repress the formation of the to the epiblast, has inductive properties that can change the original axis in committed cells of the epiblast. At the same fate of competent cells in the epiblast to form an ectopic time, the results showed that the epiblast is not wholly depen- embryonic axis. -
Lecture 19 Placentation and Maternal Recognition of Pregnancy
Blastulation Gap Junctions Lecture 19 Inner Cell Mass Zona Pellucida Placentation and Maternal Recognition of Pregnancy Trophectoderm Na+ [Na+] Animal Science 434 John J. Parrish H2O Tight Junctions Hatching Conceptus Growth Cow • Day 15, 1-2 mm Occurs in cow, pig and sheep Bovine • Day 18-19, 10-20 cm »9 - 11 days Spherical Embryonic Equine, Ovine Area »7 - 8 days Porcine Tubular Elongating »6 days Trophoblast Filamentous Mare remains spherical! Development of Porcine Conceptuses Elongated Day 15 Porcine from Day 10 to 12 Conceptus 5 mm Spherical 10 mm Spherical Inner Cell Mass 15 mm Tubular 150 mm Filamentous Embryo 1 Uterine Location of Elongating Pig Intrauterine Migration Ruminant Blastocyst Day 5 Corpus Luteum Bovine and Ovine Pig Intrauterine Migration Pig Intrauterine Migration Day 7 Day 12 Embryos become fixed Transuterine migration is rare in cow and ewe! Trans-uterine Migration in the Mare Gastrulation Begins Day 10 Inner Cell Mass Trophectoderm Formation Endoderm of Germ Fixation can Fixation occur in either on day Layers horn! 15 - 16 Blastocoele Corpus Cavity Luteum 2 Gastrulation Gastrulation Endoderrm Endoderrm Yolk Sack Yolk Sack Gastrula Gastrula Ectoderm Ectoderm Mesoderm Ectoderm Trophectoderm Trophectoderm Extraembryonic Coelom Yolk Sack Endoderm Endoderm Trophectoderm (Chorion) Germ Layers Placenta Formation Embryonic Amniotic Folds Ectoderm Mesoderm Endoderm Ectoderm » CNS » Circulatory » Digestive » Sense organs » Skeletal » Liver » Mammary » Muscle » Lungs glands » Reproductive » Pancreas Extraembryonic » -
Defective Decidualization During and After Severe Preeclampsia Reveals a Possible Maternal Contribution to the Etiology
Defective decidualization during and after severe preeclampsia reveals a possible maternal contribution to the etiology Tamara Garrido-Gomeza,b,c,d, Francisco Dominguezb, Alicia Quiñonerob, Patricia Diaz-Gimenob, Mirhan Kapidzicc,d, Matthew Gormleyc,d, Katherine Onac,d, Pablo Padilla-Isertee, Michael McMasterf, Olga Genbacevc,d, Alfredo Peralese,g, Susan J. Fisherc,d,h,i,1,2, and Carlos Simóna,b,g,j,1,2 aFundación Igenomix, 46980 Valencia, Spain; bInstituto Universitario IVI, Instituto de Investigación Sanitaria Hospital Clinico de Valencia INCLIVA, 46010 Valencia, Spain; cCenter for Reproductive Sciences, University of California, San Francisco, CA 94143; dDepartment of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, CA 94143; eDepartment of Obstetrics and Gynecology, Hospital Universitario La Fe, 46026 Valencia, Spain; fDepartment of Cell and Tissue Biology, University of California, San Francisco, CA 94143; gDepartment of Obstetrics and Gynecology, School of Medicine, Valencia University, 46010 Valencia, Spain; hThe Eli & Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA 94143; iDepartment of Anatomy, University of California, San Francisco, CA 94143; and jDepartment of Obstetrics and Gynecology, School of Medicine, Stanford University, Palo Alto, CA 94305 Edited by R. Michael Roberts, University of Missouri-Columbia, Columbia, MO, and approved August 11, 2017 (received for review April 20, 2017) In preeclampsia (PE), cytotrophoblast (CTB) invasion of the uterus in studying the CTB subpopulation that invades the uterine wall in and spiral arteries is often shallow. Thus, the placenta’s role has the context of this syndrome. Targeted analyses of particular mo- been a focus. In this study, we tested the hypothesis that decidual lecular families, such as the vascular-type adhesion molecules that defects are an important determinant of the placental phenotype. -
Decidua Produces a Protein That Inhibits Choriogonadotrophin Release from Human Trophoblasts
Decidua produces a protein that inhibits choriogonadotrophin release from human trophoblasts. S G Ren, G D Braunstein J Clin Invest. 1991;87(1):326-330. https://doi.org/10.1172/JCI114990. Research Article To test the hypothesis that uterine decidua may modulate trophoblast function, trophoblasts and decidual cells were isolated from term placentas by enzymatic digestion and Percoll gradient centrifugation. Placental trophoblasts were cocultured with decidual cells and trophoblasts or JEG-3 choriocarcinoma cells were incubated with medium conditioned by decidual cells (DCM) for 72-96 h. In cocultures decidual cells inhibited choriogonadotropin (hCG) release from trophoblasts by 75% in comparison with controls (P less than 0.001). The DCM contained a factor that markedly inhibited hCG release from trophoblasts and JEG cells in vitro compared with controls. The inhibitory effect of the factor on hCG release was dose dependent, and could be eliminated by boiling the DCM for 30 min or proteolytic enzyme treatment. Ultrafiltration and Sephadex G-50 fractionation of the DCM indicated that the apparent molecular mass was 7,000-10,000 D. DCM also inhibited the stimulatory effect of exogenous cAMP on hCG secretion by JEG-3 cells, suggesting that DCM may interfere with activation of the cAMP-dependent protein kinases or transcription of hCG genes. These results suggest that the release of trophoblast hCG is under local paracrine control, regulated in part by a protein released by decidual cells. Find the latest version: https://jci.me/114990/pdf Decidua Produces a Protein that Inhibits Choriogonadotrophin Release from Human Trophoblasts Song-Guang Ren and Glenn D. -
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. -
Cell Fate in the Early Mouse Embryo: Sorting out the Influence of Developmental History on Lineage Choice
Reproductive BioMedicine Online (2011) 22, 521– 524 www.sciencedirect.com www.rbmonline.com COMMENTARY Cell fate in the early mouse embryo: sorting out the influence of developmental history on lineage choice Samantha A Morris Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK; University of Cambridge, Department of Physiology, Development and Neurobiology, Downing Street, Cambridge CB2 3DY, UK E-mail address: [email protected]. Abstract In early mouse embryos the first cell-fate decision segregates two cell populations: the outer trophectoderm (TE) and inner cell mass (ICM). Cells are primarily directed to the ICM in two waves of asymmetric division at the 8–16-cell and 16–32-cell stage transition – the first and second waves, respectively. The ICM then diverges to become epiblast (EPI) which will generate the embryo/fetus and extra-embryonic primitive endoderm (PE). Two recent studies have aimed to address the developmental origins of these lineages. Morris et al. (2010) found that first-wave-internalized cells mainly generate EPI, whereas later internalized cells pro- vide PE. This trend was not reflected in an independent study (Yamanaka et al., 2010). From direct comparison of both datasets, it becomes clear that the key difference lies in the proportions of cells internalized in the two waves, impacting greatly upon fate. When the majority of ICM is derived from only the first wave, both EPI and PE must differentiate from the available cells and no pattern is observed. Frequently though, closer parity exists between cells dividing asymmetrically in the first and second waves, revealing the influence of developmental history upon fate. -
Development of Chick Development of Chick
Unit 15 Development of Chick UNIT 15 DEVELOPMENT OF CHICK StructureStructureStructure 15.1 Introduction Fully Formed Gastrula Objectives 15.6 Neurulation in Chick 15.2 Structure of Egg of Chick Mechanisms of Neural Plate 15.3 Fertilisation Formation 15.4 Cleavage and Blastulation Morphogenesis of Mesodermal Derivatives 15.5 Gastrulation 15.7 Folding of Embryo Role of Hypoblast 15.8 Development of Extra- Fate Map Embryonic Membranes The Gastrulation Process: Development of Amnion and Formation of Primitive Streak Chorion Completion of Endoderm Development of Allantois Regression of Primitive Streak 15.9 Hatching Epiboly of Ectoderm 15.10 Summary Characteristic Features of 15.11 Terminal Questions Avian Gastrulation 15.12 Answers Comparison with Amphibian Gastrulation 15.1 INTRODUCTION Different animals have evolved a variety of strategies of development. However, since all animals are related, the basic mechanism of early development has been conserved in the course of evolution, and so there are some important similarities in early embryonic development of all metazoan animals as you have already learnt in Block 3. This unit speaks about development of chick as an example of an amniote organism. Recall that amniotes are those vertebrates (reptiles, birds and mammals) that have a water sac or amnion surrounding the developing 163 Block 4 Developmental Biology of Vertebrates-II organism protecting it from the external environment. Chick has been one of the first model organisms to be studied in detail as it is easy to maintain and large enough to be manipulated surgically and genetically during all stages of development. You will study about strictly coordinated sequential changes that take place during the course of chick development viz. -
Extracellular Vesicles Secreted During Blastulation Show Viability of Bovine Embryos
158 6 REPRODUCTIONRESEARCH Extracellular vesicles secreted during blastulation show viability of bovine embryos Edwin A Mellisho, Mario A Briones, Alejandra E Velásquez, Joel Cabezas, Fidel O Castro and Lleretny Rodríguez-Álvarez Laboratory of Animal Biotechnology, Department of Animal Science, Faculty of Veterinary Science, Universidad de Concepcion, Chillan, Chile Correspondence should be addressed to L Rodríguez-Álvarez; Email: [email protected] Abstract Extracellular vesicles (EVs) secreted by blastocysts may be clinically relevant, as indicator of embryo viability on in vitro fertilization. We tested if the characteristics of EVs secreted during blastulation are related to embryo viability. Morulae were individually cultured in SOF media depleted of EVs until day 7.5 post IVF. Viable embryos were determined by a system of extended in vitro culture of bovine embryos until day 11 (post-hatching development). Afterward, a retrospective classification of blastocyst and culture media was performed based on blastulation time (early blastulation (EB) or late blastulation (LB)) and post-hatching development at day 11 (viable (V) or non-viable embryo (NV)). A total of 254 blastocysts and their culture media were classified in four groups (V-EB, NV-EB, V-LB, NV-LB). Group V-EB had a larger blastocyst diameter (170.8 μm), higher proportion of good-quality blastocysts (77%) and larger mean size of population of EVs (122.9 nm), although the highest concentration of EVs (5.75 × 109 particles/mL) were in group NV-EB. Furthermore, small RNA sequencing detected two biotypes, miRNA (86–91%) and snoRNA (9–14%), with a total of 182 and 32 respectively. In differential expression analysis of miRNAs between V versus NV blastocysts, there were 12 miRNAs upregulated and 15 miRNAs downregulated. -
The Origin of Early Primitive Streak 89
Development 127, 87-96 (2000) 87 Printed in Great Britain © The Company of Biologists Limited 2000 DEV3080 Formation of the avian primitive streak from spatially restricted blastoderm: evidence for polarized cell division in the elongating streak Yan Wei and Takashi Mikawa* Department of Cell Biology, Cornell University Medical College, 1300 York Avenue, New York, NY 10021, USA *Author for correspondence (e-mail: [email protected]) Accepted 13 October; published on WWW 8 December 1999 SUMMARY Gastrulation in the amniote begins with the formation of a cells generated daughter cells that underwent a polarized primitive streak through which precursors of definitive cell division oriented perpendicular to the anteroposterior mesoderm and endoderm ingress and migrate to their embryonic axis. The resulting daughter cell population was embryonic destinations. This organizing center for amniote arranged in a longitudinal array extending the complete gastrulation is induced by signal(s) from the posterior length of the primitive streak. Furthermore, expression of margin of the blastodisc. The mode of action of these cVg1, a posterior margin-derived signal, at the anterior inductive signal(s) remains unresolved, since various marginal zone induced adjacent epiblast cells, but not those origins and developmental pathways of the primitive streak lateral to or distant from the signal, to form an ectopic have been proposed. In the present study, the fate of primitive streak. The cVg1-induced epiblast cells also chicken blastodermal cells was traced for the first time in exhibited polarized cell divisions during ectopic primitive ovo from prestreak stages XI-XII through HH stage 3, streak formation. These results suggest that blastoderm when the primitive streak is initially established and prior cells located immediately anterior to the posterior marginal to the migration of mesoderm. -
From Trophoblast to Human Placenta
From Trophoblast to Human Placenta (from The Encyclopedia of Reproduction) Harvey J. Kliman, M.D., Ph.D. Yale University School of Medicine I. Introduction II. Formation of the placenta III. Structure and function of the placenta IV. Complications of pregnancy related to trophoblasts and the placenta Glossary amnion the inner layer of the external membranes in direct contact with the amnionic fluid. chorion the outer layer of the external membranes composed of trophoblasts and extracellular matrix in direct contact with the uterus. chorionic plate the connective tissue that separates the amnionic fluid from the maternal blood on the fetal surface of the placenta. chorionic villous the final ramification of the fetal circulation within the placenta. cytotrophoblast a mononuclear cell which is the precursor cell of all other trophoblasts. decidua the transformed endometrium of pregnancy intervillous space the space in between the chorionic villi where the maternal blood circulates within the placenta invasive trophoblast the population of trophoblasts that leave the placenta, infiltrates the endo– and myometrium and penetrates the maternal spiral arteries, transforming them into low capacitance blood channels. Sunday, October 29, 2006 Page 1 of 19 From Trophoblasts to Human Placenta Harvey Kliman junctional trophoblast the specialized trophoblast that keep the placenta and external membranes attached to the uterus. spiral arteries the maternal arteries that travel through the myo– and endometrium which deliver blood to the placenta. syncytiotrophoblast the multinucleated trophoblast that forms the outer layer of the chorionic villi responsible for nutrient exchange and hormone production. I. Introduction The precursor cells of the human placenta—the trophoblasts—first appear four days after fertilization as the outer layer of cells of the blastocyst. -
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