Placenta • the Syncytiotrophoblast Grows Into Endometrium
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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. -
Human Pluripotent Stem Cells As a Model of Trophoblast Differentiation in Both Normal Development and Disease
Human pluripotent stem cells as a model of trophoblast differentiation in both normal development and disease Mariko Horiia,b,1, Yingchun Lia,b,1, Anna K. Wakelanda,b,1, Donald P. Pizzoa, Katharine K. Nelsona,b, Karen Sabatinib,c, Louise Chang Laurentb,c, Ying Liud,e,f, and Mana M. Parasta,b,2 aDepartment of Pathology, University of California, San Diego, La Jolla, CA 92093; bSanford Consortium for Regenerative Medicine, University of California, San Diego, La Jolla, CA 92093; cDepartment of Reproductive Medicine, University of California, San Diego, La Jolla, CA 92093; dDepartment of Neurosurgery, Center for Stem Cell and Regenerative Medicine, University of Texas Health Sciences Center, Houston, TX 77030; eThe Senator Lloyd and B. A. Bentsen Center for Stroke Research, University of Texas Health Sciences Center, Houston, TX 77030; and fThe Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases, University of Texas Health Sciences Center, Houston, TX 77030 Edited by R. Michael Roberts, University of Missouri–Columbia, Columbia, MO, and approved May 25, 2016 (received for review March 24, 2016) Trophoblast is the primary epithelial cell type in the placenta, a Elf5 (Ets domain transcription factor) and Eomes (Eomeso- transient organ required for proper fetal growth and develop- dermin), also have been shown to be required for maintenance of ment. Different trophoblast subtypes are responsible for gas/nutrient the TSC fate in the mouse (8, 9). exchange (syncytiotrophoblasts, STBs) and invasion and maternal Significantly less is known about TE specification and the TSC vascular remodeling (extravillous trophoblasts, EVTs). Studies of niche in the human embryo (10, 11). -
Mammalogy Lecture 12
Mammalogy Lecture 11 - Reproduction I: General Patterns I. Obviously, reproduction is a very important aspect of biology and whole courses are dedicated to it. It’s easy to understand why reproductive traits would be subject to strong selection because of their direct effects on fitness. II. As we might expect, there are three basic types of mammalian reproduction. These correspond to the three major groups of mammals. Differences among these types reflect the degree of intimacy of fetal-maternal contact. A. Monotreme Type - Retain the primitive amniote pattern, but add a period of lactation. - Egg is very large at ovulation, about 3 mm. It moves down the oviduct where it is fertilized, then it’s coated with albumin, then a shell is laid down by a shell gland, and the shell is mineralized (with CaCO3). - Embryo spends 2-3 weeks in the uterus, then it’s laid. It’s large, 15 mm, when it’s laid. - Embryo growth is supported entirely by the yolk that’s enclosed in the egg. B. Metatherian type: - In some superficial ways it’s similar to monotremes, in that metatherians retain a shell membrane around the fertilized egg; a shell gland is present in Müllerian ducts. - However the shell is never mineralized and young are born live after only ca. 12 days, as we’ve seen, they are very altricial (poorly developed). - Initial intrauterine growth is supported by maternally by a placenta. - Metatherian placenta is the choriovitelline type - yolk-sac placenta (Eutherian placenta is called chorioallantoic placenta) C. Placenta Formation - Let’s look at formation of the placenta in Meta- & Eutherians. -
Adhesive and Degradative Properties of Human Placental Cytotrophoblast Cells in Vitro Susan J
Adhesive and Degradative Properties of Human Placental Cytotrophoblast Cells In Vitro Susan J. Fisher, Tian-yi Cui, Li Zhang, Lynn Hartman, Kim Grahl, Zhang Guo-Yang, John Tarpey, and Caroline H. Damsky Departments of Stomatology, Anatomy, and Pharmaceutical Chemistry, University of California at San Francisco, San Francisco, California 94143 Abstract. Human fetal development depends on the ponents into the medium. No similar degradative ac- embryo rapidly gaining access to the maternal circula- tivity was observed when second or third trimester tion. The trophoblast cells that form the fetal portion cytotrophoblast cells, first trimester human placental of the human placenta have solved this problem by fibroblasts, or the human choriocarcinoma cell lines transiently exhibiting certain tumor-like properties. BeWo and JAR were cultured on radiolabeled matrices. Thus, during early pregnancy fetal cytotrophoblast To begin to understand the biochemical basis of this cells invade the uterus and its arterial network. This degradative behavior, the substrate gel technique was process peaks during the twelfth week of pregnancy used to analyze the cell-associated and secreted pro- and declines rapidly thereafter, suggesting that the teinase activities expressed by early, mid, and late highly specialized, invasive behavior of the cytotropho- gestation cytotrophoblasts. Several gelatin-degrading blast cells is closely regulated. Since little is known proteinases were uniquely expressed by early gesta- about the actual mechanisms involved, we developed tion, invasive cytotrophoblasts, and all these activities an isolation procedure for cytotrophoblasts from could be abolished by inhibitors of metalloproteinases. placentas of different gestational ages to study their By early second trimester, the time when cytotropho- adhesive and invasive properties in vitro. -
MA 5.4 NUMA SI GA RBHAVIKA S KRAM Completed Fetus in Prsava- Vastha Rasanufj*^SIK GARBHAVRUDHI
MA 5.4 NUMA SI GA RBHAVIKA S KRAM Completed Fetus in prsava- vastha rASANUfJ*^SIK GARBHAVRUDHI I N Ayurvedic classics, the embryonit*««,^jie.uaJf6f'ment has been narrated monthwise while the modern Medical literature has considered the development of embryo in months as well as in weeks. "KALALAV/ASTHA (first month) ^ T ^.?1T. 3/14 Susruta and both Vagbhattas us.ed the word 'K a la la ' forthe shape of the embryo in the first month of intrauterine life. I Caraka has described the first month embryo as a mass ofcells like mucoid character in which all body parts though present are not conspicuous. T Incorporated within it all the five basic elements, ' Panchmah'abhuta' i.e. Pruthvi, Ap , Teja, Vayu and Akas . During the first month the organs of Embryo are both manifested and latent. It is from this stage of Embryo that various organs of the fetus develop, thus they are menifested. But these organs are not well menifested for differentiation and recongnisiation hence they are simultenously described as latent as well as manifested. 3T.f.^. 1/37 Astang - hrudayakar has described the embryo of first month as 'Kalala' but in 'avyakta' form. The organs of an embryo is in indistingushed form. Modern embryologist has described this first month development in week divisions. First Week - No fertile ova of the first week has been examined. Our knowledge of the first week of I embryo is of other mammals as amphibian. The egg is fertilised in the upper end of the uterine tube, and segments into about cells, before it I passes in to the uterus, it continues to segment and develop into a blastocyst (Budbuda) with a trophoblastic cells and inner cell mass. -
What Is the Role of the Placenta—Does It Protect Against Or Is It a Target for Insult?
Teratology Primer, 3rd Edition www.teratology.org/primer What Is the Role of the Placenta—Does It Protect Against or Is It a Target for Insult? Richard K. Miller University of Rochester School of Medicine & Dentistry Rochester, New York The placenta is not just a barrier but has many functions that are vital to the health of the embryo/fetus. The placenta is the anchor, the conduit, and the controller of pregnancy—and it can also be a target for toxicant action. The placenta encompasses not only the chorioallantoic placenta but all of its extraembryonic membranes (chorion/amnion) and the yolk sac. (Figure 1). The placenta and its membranes secure the embryo and fetus to the decidua (uterine lining) and release a variety of steroid and protein hormones that characterize the physiology of the pregnant female. Figure 1. Placental Structure in the Mouse. Figures depict early development of the mouse conceptus at embryonic days (E3.5, E7.5, E12.5). In the fetus, the visceral yolk sac (vYS) inverts and remains active throughout the entire gestation providing for transfer of selective large molecules, e.g., immunoglobulins IgG and vitamin B12. Abbreviations: Al, allantois; Am, amnion; Ch, chorion; Dec, decidua; Emb, embryo; Epc, ectoplacental cone; ICM, inner cell mass; Lab, Labyrinth; pYS, parietal yolk sac; SpT, spongiotrophoblast; TCG, trophoblast giant cell; Umb Cord, umbilical cord; vYS, visceral yolk sac; C-TGC, maternal blood canal trophoblast giant cell; P-TGC, parietal trophoblast giant cell; S-TGC, sinusoidal trophoblast giant cell; SpA-TGC, Spiral artery-associated trophoblast giant cell; Cyan-trophectoderm and trophoblast lineage, Black- inner cell mass and embryonic ectoderm; Gray -endoderm, Red-maternal vasculature, Purple-mesoderm, Yellow- decidua, Pink-fetal blood vessels in labyrinth. -
Equine Placenta – Marvelous Organ and a Lethal Weapon
Equine placenta – marvelous organ and a lethal weapon Malgorzata Pozor, DVM, PhD, Diplomate ACT Introduction Placenta has been defined as: „an apposition between parent (usually maternal) and fetal tissue in order to establish physiological exchange” (1). Another definition of this important organ was proposed by Steven and Morris: „a device consisting of one or more transport epithelia located between fetal and maternal blood supply” (2). The main function of placenta is to provide an interface between the dam and the the fetus and to allow the metabolic exchange of the the nutrients, oxygen and waste material. The maternal circulation is brought into a close apposition to the fetal circulation, while a separation of these two circulatory systems remain separated (3). A degree and complexity of this „intimate relationship” varies greately between species mostly due to the structural diversity of the extraembryonic membranes of the vertebrates. The early feto-maternal exchange in the equine pregnancy is established as early as on day 22 after fertilization. The fetal and choriovitellin circulations are already present, the capsule ruptures and the allantois is already visible (4). The allantois starts expanding by day 32 and vascularizes approximately 90% of the chorion and fuses with it to form chorioallantois by day 38 of gestation (5). The equine placenta continues increasing its complexity till approximately day 150 of gestation. Equids have epitheliochorial placenta, there are six leyers separating maternal and fetal circulation, and there are no erosion of the luminal, maternal epithelium, like in ruminants (6). Thousands of small chorionic microvilli develop and penetrate into endometrial invaginations. -
4 Extraembryonic Membranes
Implantation, Extraembryonic Membranes, Placental Structure and Classification A t t a c h m e n t and Implantation Implantation is the first stage in development of the placenta. In most cases, implantation is preceded by a close interaction of embryonic trophoblast and endometrial epithelial cells that is known as adhesion or attachment. Implantation also is known as the stage where the blastocyst embeds itself in the endometrium, the inner membrane of the uterus. This usually occurs near the top of the uterus and on the posterior wall. Among other things, attachment involves a tight intertwining of microvilli on the maternal and embryonic cells. Following attachment, the blastocyst is no longer easily flushed from the lumen of the uterus. In species that carry multiple offspring, attachment is preceeded by a remarkably even spacing of embryos through the uterus. This process appears to result from uterine contractions and in some cases involves migration of embryos from one uterine horn to another (transuterine migration). The effect of implantation in all cases is to obtain very close apposition between embryonic and maternal tissues. There are, however, substantial differences among species in the process of implantation, particularly with regard to "invasiveness," or how much the embryo erodes into maternal tissue. In species like horses and pigs, attachment and implantation are essentially equivalent. In contrast, implantation in humans involves the embryo eroding deeply into the substance of the uterus. •Centric: the embryo expands to a large size before implantation, then remains in the center of the uterus. Examples include carnivores, ruminants, horses, and pigs. •Eccentric: The blastocyst is small and implants within the endometrium on the side of the uterus, usually opposite to the mesometrium. -
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. -
Placenta-4-2-15.Pdf
3.2.2015 PLACENTA Dr. Archana Rani Associate Professor Department of Anatomy KGMU UP, Lucknow Implantation • Begins on the 6th day after fertilization • Embedding of blastocyst in the wall of uterus • Disappearance of zona pellucida • Cells of the trophoblast stick to the endometrium • After implantation of the embryo, the uterine endometrium is called the decidua Implantation Site of implantation • Normal site - At the junction of fundus and posterior wall of uterus - At upper uterine segment Interstitial Implantation The Decidua After implantation of the embryo, the uterine endometrium is called the decidua. Subdivisions of Decidua Formation of Chorionic Villi • Villi are the essential functional elements of the placenta. • Small finger like processes. • Surrounded by maternal blood. • Fetal blood circulates in their substance through capillaries. • Called as Chorionic villi as arises as offshoots from chorion. Stages in formation of Chorionic villi Early stages in formation of Chorionic villi (9th day) Formation of Chorionic villi Lacunar spaces filled with maternal blood Primary Villus (Day 13-14) All elements (syncytium, cytotrophoblast and extraembryonic mesoderm) take part in formation of chorionic villi. Three stages in formation of chorionic villi are seen: Primary villus: central core of cytotrophoblast covered by a layer of syncytiotrophoblast. Adjoining villi are separated by an intervillous space. Secondary Villus (Early 3rd week) Central core of extraembryonic mesoderm covered successively by cyto and syncytiotrophoblasts. Tertiary Villus (End of 3rd week) Appearance of blood vessels in the mesoderm forming core of each villus. Formation of cytotrophoblastic shell Anchoring villi & its subdivisions Fully formed Placenta (4th month) DEFINITION • Placenta is a fetomaternal organ which is the primary site of nutrient and gas exchange between the fetus and the mother. -
Single-Cell Transcriptomics of the Human Placenta: Inferring the Cell Communication Network of the Maternal-Fetal Interface
Downloaded from genome.cshlp.org on September 26, 2021 - Published by Cold Spring Harbor Laboratory Press Research Single-cell transcriptomics of the human placenta: inferring the cell communication network of the maternal-fetal interface Mihaela Pavličev,1,2 Günter P. Wagner,3,4,5,6 Arun Rajendra Chavan,3 Kathryn Owens,7 Jamie Maziarz,3 Caitlin Dunn-Fletcher,2 Suhas G. Kallapur,1,2 Louis Muglia,1,2 and Helen Jones7,8 1Center for Prevention of Preterm Birth, Perinatal Institute, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio 45229, USA; 2Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA; 3Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut 06511, USA; 4Yale Systems Biology Institute, Yale University, West Haven, Connecticut 06516, USA; 5Department of Obstetrics, Gynecology and Reproductive Sciences, Yale Medical School, Yale University, New Haven, Connecticut 06510, USA; 6Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan 48201, USA; 7Center for Fetal Cellular and Molecular Therapy, Perinatal Institute, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio 45229, USA; 8Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA Organismal function is, to a great extent, determined by interactions among their fundamental building blocks, the cells. In this work, we studied the cell-cell interactome of fetal placental trophoblast cells and maternal endometrial stromal cells, using single-cell transcriptomics. The placental interface mediates the interaction between two semiallogenic individuals, the mother and the fetus, and is thus the epitome of cell interactions. To study these, we inferred the cell-cell interactome by assessing the gene expression of receptor-ligand pairs across cell types. -
Placental Pathology: Its Impact on Explaining Prenatal and Perinatal Death
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2004 Placental pathology: its impact on explaining prenatal and perinatal death Stallmach, Thomas ; Hebisch, Gundula Abstract: This review considers six main situations in which pathologists are expected to report and interpret placental messages for obstetricians, neonatologists and, indirectly, parents: (1) abortion is the body’s corrective response to the embryonic defect suggested by malformed chorionic villi; (2) in- fection causing chorionic villous inflammation is specific and haematogenous; pathogen identification is mandatory, in contrast to chorioamnionitis caused by increased local immunosuppression allowing indis- criminate bacterial entry; (3) prematurity and (4) intrauterine growth restriction are often associated with pregnancy-specific disease (pre-eclampsia) or pre-existing maternal conditions (systemic lupus); parental studies may improve outcome in subsequent pregnancies; (5) intrauterine death near term is often due to placental dysmaturity featuring a severely reduced number of syncytiocapillary membranes; it accounts for the death in utero of 3 in 1000 pregnancies; detection helps to minimise recurrence in subsequent pregnancies; (6) twins are best confirmed as monozygous by the absence of chorionic tissue in thedivid- ing membranes; most monochorionic twins have vascular connections whose detailed analysis is requested only if there are inter-twin differences in growth and colour. From a formal point of view, many morebits of pathology than discussed in this review can be found in placentas and, with the advances in ultrasonog- raphy, might even be seen prior to birth. The extent of such a disturbance might ultimately affect fetal growth, which is amenable to prenatal detection offering the chances for an appropriate management.