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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. -
Formation of Germ Layers (Second & Third Week of Development)
8.12.2014 Formation of Germ Layers (Second & Third week of Development) Dr. Archana Rani Associate Professor Department of Anatomy KGMU UP, Lucknow Day 8 • Blastocyst is partially embedded in the endometrial stroma. • Trophoblast differentiates into 2 layers: (i) Cytotrophoblast (ii) Syncytiotrophoblast • Cytotrophoblast shows mitotic division. Day 8 • Cells of inner cell mass (embryoblast) also differentiate into 2 layers: (i) Hypoblast layer (ii) Epiblast layer • Formation of amniotic cavity and embryonic disc. Day 9 • The blastocyst is more deeply embedded in the endometrium. • The penetration defect in the surface epithelium is closed by a fibrin coagulum. Day 9 • Large no. of vacuoles appear in syncytiotrophoblast which fuse to form lacunae which contains embryotroph. Day 9 • Hypoblast forms the roof of the exocoelomic cavity (primary yolk sac). • Heuser’s (exocoelomic membrane) • Extraembryonic mesoderm Day 11 & 12 • Formation of lacunar networks • Extraembryonic coelom (chorionic cavity) • Extraembryonic somatic mesoderm • Extraembryonic splanchnic mesoderm • Chorion Day 13 • Implantation bleeding • Villous structure of trophoblast. • Formation of Primary villi • Secondary (definitive) yolk sac • Chorionic plate (extraembronic mesoderm with cytotrophoblast) Third week of Development • Gastrulation (formation of all 3 germ layers) • Formation of primitive streak • Formation of notochord • Differentiation of 3 germ layers from Bilaminar to Trilaminar germ disc Formation of Primitive Streak (PS) • First sign of gastrulation • On 15th day • Primitive node • Primitive pit • Formation of mesenchyme on 16th day • Formation of embryonic endoderm • Intraembryonic mesoderm • Ectoderm • Epiblast is the source of all 3 germ layers Fate of Primitive Streak • Continues to form mesodermal cells upto early part of 4th week • Normally, the PS degenerates & diminishes in size. -
Morphological Characterization of Pre-And Peri-Implantation in Vitro
REPRODUCTIONRESEARCH Morphological characterization of pre- and peri-implantation in vitro cultured, somatic cell nuclear transfer and in vivo derived ovine embryos P Tveden-Nyborg, T T Peura1, K M Hartwich2, S K Walker2 and P Maddox-Hyttel Department of Animal and Veterinary Basic Sciences, Royal Veterinary and Agricultural University, Groennegaardsvej 7, DK-1870 Frederiksberg C, Denmark, 1Sydney IVF Ltd, 4 O’Connell Street, Sydney, NSW 2000, Australia and 2South Australian Research and Development Institute, Turretfield Research Centre, Rosedale, SA 5350, Australia Correspondence should be addressed to Pernille Tveden-Nyborg; Email: [email protected] Abstract The processes of cellular differentiation were studied in somatic cell nuclear transfer (SCNT), in vitro cultured (IVC) and in vivo developed (in vivo) ovine embryos on days 7, 9, 11, 13, 17 and 19. SCNT embryos were constructed from in vitro matured oocytes and granulosa cells, and IVC embryos were produced by in vitro culture of in vivo fertilized zygotes. Most SCNT and IVC embryos were transferred to recipients on day 6 while some remained in culture for day 7 processing. In vivo embryos were collected as zygotes, transferred to intermediate recipients and retransferred to final recipients on day 6. All embryos were processed for examination by light and transmission electron microscopy or immunohistochemical labelling for alpha-1-fetoprotein and vimentin. Overall, morphological development of in vivo embryos was superior to IVC and SCNT embryos. Day 7 and particularly day 9 IVC and SCNT embryos had impaired hypoblast development, some lacking identifiable inner cell masses. On day 11, only in vivo and IVC embryos had developed an embryonic disc, and gastrulation was evident in half of in vivo embryos and one IVC embryo. -
From Hatching Into Fetal Life in the P E in the P E in The
R.C. Chebel. 2011. Use of Applied Reproductive Technologies (FTAI, FTET) to Improve the Reproductive Efficiency in Dairy Cattle. Acta Scientiae Veterinariae. 39(Suppl 1): s203 - s221. Acta Scientiae Veterinariae, 2011. 39(Suppl 1): s203 - s221. ISSN 1679-9216 (Online) From Hatching into Fetal Life in the Pig Poul Hyttel, Kristian M. Kamstrup & Sara Hyldig ABSTRACT Background: Potential adverse effects of assisted reproductive technologies may have long term consequences on embryonic and fetal development. However, the complex developmental phases occurring after hatching from the zona pellucida are less studied than those occurring before hatching. The aim of the present review is to introduce the major post-hatching developmental features bringing the embryo form the blastocyst into fetal life in the pig. Review: In the pre-hatching mouse blastocyst, the pluripotency of the inner cell mass (ICM) is sustained through expression of OCT4 and NANOG. In the pre-hatching porcine blastocyst, a different and yet unresolved mechanism is operating as OCT4 is expressed in both the ICM and trophectoderm, and NANOG is not expressed at all. Around the time of hatching, OCT4 becomes confined to the ICM. In parallel, the ICM is divided into a ventral cell layer, destined to form the hypoblast, and a dorsal cell mass, destined to form the epiblast. The hypoblast gradually develops into a complete inner lining along the epiblast and the trophectoderm. Upon hatching (around Day 7-8 of gestation), the trophectoderm covering the developing epiblast (Rauber´s layer) is lost and the embryonic disc is formed by development of a cavity in the epiblast, which subsequently “unfolds” resulting the establishment of the disc. -
Embryology of the Spine and Associated Congenital Abnormalities Kevin M
The Spine Journal 5 (2005) 564–576 Review Article Embryology of the spine and associated congenital abnormalities Kevin M. Kaplan, MDa,*, Jeffrey M. Spivak, MDa,b, John A. Bendo, MDa,b aNew York University-Hospital for Joint Diseases, Department of Orthopaedic Surgery, 14th Floor, 301 East 17th Street, New York, NY 10003, USA bHospital for Joint Diseases Spine Center, Department of Orthopaedic Surgery, 14th Floor, 301 East 17th Street, New York, NY 10003, USA Received 11 June 2004; accepted 18 October 2004 Abstract BACKGROUND CONTEXT: The spine is a complex and vital structure. Its function includes not only structural support of the body as a whole, but it also serves as a conduit for safe passage of the neural elements while allowing proper interaction with the brain. Anatomically, a variety of tissue types are represented in the spine. Embryologically, a detailed cascade of events must occur to result in the proper formation of both the musculoskeletal and neural elements of the spine. Alterations in these embryologic steps can result in one or more congenital abnormalities of the spine. Other body systems forming at the same time embryologically can be affected as well, resulting in associated defects in the cardiopulmonary system and the gastrointestinal and genito- urinary tracts. PURPOSE: This article is to serve as a review of the basic embryonic development of the spine. We will discuss the common congenital anomalies of the spine, including their clinical presentation, as examples of errors of this basic embryologic process. STUDY DESIGN/SETTING: Review of the current literature on the embryology of the spine and associated congenital abnormalities. -
Introduction to Human Development 3
Introduction to Human 1 Development DEVELOPMENTAL PERIODS, 1 Embryology in the Middle Ages, 4 Stages of Embryonic Development, 1 The Renaissance, 5 Postnatal Period, 1 GENETICS AND HUMAN DEVELOPMENT, 6 Infancy, 1 MOLECULAR BIOLOGY OF HUMAN Childhood, 1 DEVELOPMENT, 7 Puberty, 1 DESCRIPTIVE TERMS IN EMBRYOLOGY, 7 Adulthood, 2 CLINICALLY ORIENTED PROBLEMS, 9 SIGNIFICANCE OF EMBRYOLOGY, 2 HISTORICAL GLEANINGS, 4 Ancient Views of Human Embryology, 4 Human development is a continuous process that begins weeks), when embryonic and early fetal development is when an oocyte (ovum) from a female is fertilized by a sperm occurring. (spermatozoon) from a male to form a single-celled zygote (Fig. 1.1). Cell division, cell migration, programmed cell POSTNATAL PERIOD death (apoptosis), differentiation, growth, and cell rearrange- ment transform the fertilized oocyte, a highly specialized, This is the period occurring after birth. Explanations of totipotent cell, the zygote, into a multicellular human being. frequently used postnatal developmental terms and periods Most developmental changes occur during the embryonic follow. and fetal periods; however, important changes occur during later periods of development: the neonatal period (first 4 INFANCY weeks), infancy (first year), childhood (2 years to puberty), and adolescence (11 to 19 years). Infancy is the period of extrauterine life, roughly the first year after birth. An infant age 1 month or younger is called a neonate (newborn). The transition from intrauterine to DEVELOPMENTAL PERIODS extrauterine existence requires many critical changes, especially in the cardiovascular and respiratory systems. If It is customary to divide human development into prenatal neonates survive the first crucial hours after birth, their (before birth) and postnatal (after birth) periods. -
General Embryology-2-Early Development
Fertilization Process of fusion of male and female gametes in the ampullary region of the fallopian tube. • Entrance of sperms in the female genital tract. • Capacitation • Acrosome reaction •Penetration of corona radiata •Penetration of zona pellucida •Fusion of oocyte and sperm cell membrane Response of ovum •Cortical and zona reactions. •Resumption of Meiosis II •Metabolic activation of the egg. Results of fertilization •Determination of sex •Restoration of diploid number of chromosomes •Initiation of cleavage Zygote is -2 celled at 30 hrs -4 celled at 40 hours -12 celled at 3 days -16 celled at 4 days •This 16 celled stage is –morula •Compaction: morula cells form an inner and outer cell mass •zona pellucida disappears at 4th day 30 8 69 5th day 6th day SUMARY OF DEVELOPMENT IN 1st WEEK AFTER FERILIZATION Cleavage Morula Blastocyst formation Implantation 8th day 9th day 12th day 13th day Connecting stalk SUMARY OF DEVELOPMENT IN 2ND WEEK Completion of embedding. TROPHOBLASTS EMBRYOBLASTS • Differentiate into • Differentiate into cytotrophoblast & epiblast & hypoblast syncytiotrophoblast • Formation of amnioblasts and • Lacunae formed & amniotic cavity beginning of • Formation of primary and uteroplacental circulation secondary yolk sacs • Formation of primary villi • Formation of extraembryonic Decidual Reaction: mesoderm; ee coelom (chorionic cavity); -Oedema of stroma ee somatopleuric and -Enlarged glands splanchnopleuric layers -Increased Glycogen content of epithelial cells -Congestion ECTOPIC IMPLANTATION • Tubal • Ampullary • Interstitial • Low uterine •Ovarian • Secondary abdominal NOTOCHORD • Provides midline axis to the body. • Induces formation of neural plate. REMAINS OF NOTOCHORD 1. Nucleus pulposus. 2. Apical ligament. 3. Its cranial part is incorporated into basiocciput and basisphenoid. Approx. Age (Days) No. -
2. Blastogenesis. Implantation. Gastrulation. Notochord. Somites
Z. Tonar, M. Králíčková: Outlines of lectures on embryology for 2 nd year student of General medicine and Dentistry License Creative Commons - http://creativecommons.org/licenses/by-nc-nd/3.0/ 2. Blastogenesis. Implantation. Gastrulation. Notochord. Somites. Upon fertilization − restoration of the diploid number of chromosome − individual karyotype (set of chromosomes) completed − chromosomal determination of sex of the new individual (46 XX, 46XY) − mitoses = cleavage − zygote → blastomeres, un#l the day 4 s#ll within the zona pellucida o 30 hours: 2 blastomeres o 40 hours: 4 blastomeres o 3 days 16 blastomeres = morula − day 4 o late morula hatchin from the )P o cavities fusin into blastocoelom " blastocyst − day 6: outer + inner blastomeres et specialized to: o trophoblast cells later on ives rise to extraembryonic structures, fetal membranes o embryoblast later on ives rise to epiblast and hypoblast (embryonic,animal pole) Cleavage and gastrulation in man − oocyte o oli olecithal (little yolk only) o isolecithal (even distribution of yolk) − cleava e o total (the whole volume under oes the cleava e) o e-ual (uniform size of blastomeres) − astrulation o .euterostomia (Echinodermata, 0emochordata, 1hordata) o delamination (mi ration of cell layers) instead of inva ination Morula and blastocyst − day 3: 16 blastomeres = morula − day 4: o hatchin of the late morula o outer cell mass = trophoblast o inner cell mass = embryoblast o blastocoelom " blastocyst Implantation (nidation) − mostly in anterior or posterior uterine wall, in the cranial third of the uterine body − cave: ectopic implantation ( raviditas extrauterina 2 3E4) − day 6211 − adhesion of the trophoblast to the endometrium (secretory phase) o selectins produced by the trophoblast bind the oli osaccharides on the endometrial surface 1/5 Z. -
Reproductionresearch
REPRODUCTIONRESEARCH Staging of ovine embryos and expression of the T-box genes Brachyury and Eomesodermin around gastrulation Michel Guillomot, Annick Turbe, Isabelle Hue and Jean-Paul Renard UMR Biologie du De´veloppement et Reproduction, Institut National de la Recherche Agronomique, 78352 Jouy-en-Josas, France Correspondence should be addressed to Michel Guillomot; Email: [email protected] Abstract The high rates of embryonic mortalities which follow in vitro production of ruminant embryos have emphasized the need for increased knowledge of early development. It is likely that early failures in embryonic development and placenta formation involve abnormal differentiation of mesoderm. The aim of this study was to investigate the pattern of expression of two T-box genes known to control the gastrulation process, Brachyury and Eomesodermin, by whole-mount in situ hybridization. To allow a more precise comparison of both expression patterns between embryos, we describe a new staging of pre-implanted ovine embryos by gross morphology and histology from pre-gastrulation stages to the beginning of neurulation. In pre-streak embryos primitive mesoderm cells delaminated in between the primitive endoderm and the epiblast. At that stage, no expression of Brachyury or Eomesodermin could be detected in the embryos. Early expression of both T-genes was observed by the early-streak stages in epiblast cells located close to the presumptive posterior pole of the embryos. Later on, during gas- trulation both genes followed a pattern of expression similar to the ones described in other mammals. These observations suggest that other genes, which remain to be identified, are responsible for extra-embryonic mesoderm differentiation in rumi- nant embryos. -
Redalyc.From Hatching Into Fetal Life in The
Acta Scientiae Veterinariae ISSN: 1678-0345 [email protected] Universidade Federal do Rio Grande do Sul Brasil Hyttel, Poul; Kamstrup, Kristian M.; Hyldig, Sara From Hatching into Fetal Life in the Pig Acta Scientiae Veterinariae, vol. 39, núm. 1, 2011, pp. s203-s221 Universidade Federal do Rio Grande do Sul Porto Alegre, Brasil Available in: http://www.redalyc.org/articulo.oa?id=289060016027 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative R.C. Chebel. 2011. Use of Applied Reproductive Technologies (FTAI, FTET) to Improve the Reproductive Efficiency in Dairy Cattle. Acta Scientiae Veterinariae. 39(Suppl 1): s203 - s221. Acta Scientiae Veterinariae, 2011. 39(Suppl 1): s203 - s221. ISSN 1679-9216 (Online) From Hatching into Fetal Life in the Pig Poul Hyttel, Kristian M. Kamstrup & Sara Hyldig ABSTRACT Background: Potential adverse effects of assisted reproductive technologies may have long term consequences on embryonic and fetal development. However, the complex developmental phases occurring after hatching from the zona pellucida are less studied than those occurring before hatching. The aim of the present review is to introduce the major post-hatching developmental features bringing the embryo form the blastocyst into fetal life in the pig. Review: In the pre-hatching mouse blastocyst, the pluripotency of the inner cell mass (ICM) is sustained through expression of OCT4 and NANOG. In the pre-hatching porcine blastocyst, a different and yet unresolved mechanism is operating as OCT4 is expressed in both the ICM and trophectoderm, and NANOG is not expressed at all. -
Divisions of Embryology
DivisionsDivisions ofof embryologyembryology GeneralGeneral eembryologymbryology Gametogenesis: conversion of germ cells into male and female gametes 1st week of development: ovulation to implantation 2nd week of development: bilaminar germ disc 3rd week of development: trilaminar germ disc 3rd to 8th week: embryonic period 3rd month to birth: fetus and placenta SpecialSpecial eembryologymbryology Skeletal system Cardiovascular system Respiratory syste m Nervous system, etc …. systems GASTRULATION (Gr., belly ) BBilaminarilaminar diskdisk →→ trilaminartrilaminar diskdisk TheThe embryoembryo hashas reachedreached aa pointpoint ofof balancebalance inin itsits efeffortsforts toto :: draw nourishment from the mother (trophoblast layers and their derivatives) to be protected against cellular assault (several ensheathing layers & protective cavities) to harbor enough of its own food (secondary yolk sac ) TimeTime toto movemove –– thethe innerinner cellcell massmass derivativesderivatives differentiatedifferentiate intointo thethe threethree functionalfunctional cellcell layerslayers ofof lifelife outer layer → protective and sensitive inner layer → energy -absorbing connective layer between them → contractile movement GastrulationGastrulation startsstarts withwith primitiveprimitive streakstreak cut trophoblast 90 ° rotation PrimitivePrimitive streakstreak –– dayday 1414 Formed by cells of the epiblast which choose one of the two fates: pass deep to the epiblast layer to form the populations of cells within the embryo -
Gene Expression Analysis of Bovine Embryonic Disc, Trophoblast and Parietal Hypoblast at the Start of Gastrulation
The University of Notre Dame Australia ResearchOnline@ND Medical Papers and Journal Articles School of Medicine 2017 Gene expression analysis of bovine embryonic disc, trophoblast and parietal hypoblast at the start of gastrulation P Pfeffer C Smith The University of Notre Dame Australia, [email protected] P Maclean D Berg Follow this and additional works at: https://researchonline.nd.edu.au/med_article Part of the Medicine and Health Sciences Commons This article was originally published as: Pfeffer, P., Smith, C., Maclean, P., & Berg, D. (2017). Gene expression analysis of bovine embryonic disc, trophoblast and parietal hypoblast at the start of gastrulation. Zygote, 25 (3), 265-278. http://doi.org/10.1017/S0967199417000090 This article is posted on ResearchOnline@ND at https://researchonline.nd.edu.au/med_article/883. For more information, please contact [email protected]. This article originally published in Zygote available at https://www.cambridge.org/core/journals/zygote/article/gene-expression-analysis-of-bovine- embryonic-disc-trophoblast-and-parietal-hypoblast-at-the-start-of- gastrulation/797D7C7B660E4A0B021F3FB01D81F5FE Pfeffer, P., Smith, C., Maclean, P., Berg, D. (2017). Gene expression analysis of bovine embryonic disc, trophoblast and parietal hypoblast at the start of gastrulation. Zygote. 25(3), 265-278. doi:10.1017/S0967199417000090 Zygote Ge ne expression analysis of bovine embryonic disc, trophoblast and parietal hypoblast at the start of gastrulation Journal: Zygote Manuscript ID ZYG-2017-0003.R1 Manuscript