Eye Embryology Made Simply Ridiculous
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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. -
Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
International Journal of Molecular Sciences Review Development and Maintenance of Epidermal Stem Cells in Skin Adnexa Jaroslav Mokry * and Rishikaysh Pisal Medical Faculty, Charles University, 500 03 Hradec Kralove, Czech Republic; [email protected] * Correspondence: [email protected] Received: 30 October 2020; Accepted: 18 December 2020; Published: 20 December 2020 Abstract: The skin surface is modified by numerous appendages. These structures arise from epithelial stem cells (SCs) through the induction of epidermal placodes as a result of local signalling interplay with mesenchymal cells based on the Wnt–(Dkk4)–Eda–Shh cascade. Slight modifications of the cascade, with the participation of antagonistic signalling, decide whether multipotent epidermal SCs develop in interfollicular epidermis, scales, hair/feather follicles, nails or skin glands. This review describes the roles of epidermal SCs in the development of skin adnexa and interfollicular epidermis, as well as their maintenance. Each skin structure arises from distinct pools of epidermal SCs that are harboured in specific but different niches that control SC behaviour. Such relationships explain differences in marker and gene expression patterns between particular SC subsets. The activity of well-compartmentalized epidermal SCs is orchestrated with that of other skin cells not only along the hair cycle but also in the course of skin regeneration following injury. This review highlights several membrane markers, cytoplasmic proteins and transcription factors associated with epidermal SCs. Keywords: stem cell; epidermal placode; skin adnexa; signalling; hair pigmentation; markers; keratins 1. Epidermal Stem Cells as Units of Development 1.1. Development of the Epidermis and Placode Formation The embryonic skin at very early stages of development is covered by a surface ectoderm that is a precursor to the epidermis and its multiple derivatives. -
AP-2Α and AP-2Β Cooperatively Function in the Craniofacial Surface Ectoderm to Regulate
bioRxiv preprint doi: https://doi.org/10.1101/2021.06.10.447717; this version posted June 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. AP-2α and AP-2β cooperatively function in the craniofacial surface ectoderm to regulate 2 chromatin and gene expression dynamics during facial development. 4 Eric Van Otterloo1,2,3,4,*, Isaac Milanda4, Hamish Pike4, Hong Li4, Kenneth L Jones5#, Trevor Williams4,6,7,* 6 1 Iowa Institute for Oral Health Research, College of Dentistry & Dental Clinics, University of Iowa, Iowa City, IA, 52242, USA 8 2 Department of Periodontics, College of Dentistry & Dental Clinics, University of Iowa, Iowa City, IA, 52242, USA 10 3 Department of Anatomy and Cell Biology, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242, USA 12 4 Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA 14 5 Department of Pediatrics, Section of Hematology, Oncology, and Bone Marrow Transplant, University of Colorado School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, 16 USA 6 Department of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, 18 Aurora, CO, 80045, USA 7 Department of Pediatrics, University of Colorado Anschutz Medical Campus, Children's Hospital 20 Colorado, Aurora, CO 80045, USA * Corresponding Authors 22 #Present Address: Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA 24 Keywords: Tfap2, AP-2, transcription factor, ectoderm, craniofacial, neural crest, Wnt signaling 26 bioRxiv preprint doi: https://doi.org/10.1101/2021.06.10.447717; this version posted June 10, 2021. -
Induction and Specification of Cranial Placodes ⁎ Gerhard Schlosser
Developmental Biology 294 (2006) 303–351 www.elsevier.com/locate/ydbio Review Induction and specification of cranial placodes ⁎ Gerhard Schlosser Brain Research Institute, AG Roth, University of Bremen, FB2, PO Box 330440, 28334 Bremen, Germany Received for publication 6 October 2005; revised 22 December 2005; accepted 23 December 2005 Available online 3 May 2006 Abstract Cranial placodes are specialized regions of the ectoderm, which give rise to various sensory ganglia and contribute to the pituitary gland and sensory organs of the vertebrate head. They include the adenohypophyseal, olfactory, lens, trigeminal, and profundal placodes, a series of epibranchial placodes, an otic placode, and a series of lateral line placodes. After a long period of neglect, recent years have seen a resurgence of interest in placode induction and specification. There is increasing evidence that all placodes despite their different developmental fates originate from a common panplacodal primordium around the neural plate. This common primordium is defined by the expression of transcription factors of the Six1/2, Six4/5, and Eya families, which later continue to be expressed in all placodes and appear to promote generic placodal properties such as proliferation, the capacity for morphogenetic movements, and neuronal differentiation. A large number of other transcription factors are expressed in subdomains of the panplacodal primordium and appear to contribute to the specification of particular subsets of placodes. This review first provides a brief overview of different cranial placodes and then synthesizes evidence for the common origin of all placodes from a panplacodal primordium. The role of various transcription factors for the development of the different placodes is addressed next, and it is discussed how individual placodes may be specified and compartmentalized within the panplacodal primordium. -
Endothelium Ii
Br J Ophthalmol: first published as 10.1136/bjo.42.11.667 on 1 November 1958. Downloaded from Brit. J. Ophthal. (1958) 42, 667. STUDIES ON THE CORNEAL AND TRABECULAR ENDOTHELIUM II. ENDOTHELIUM OF THE ZONE OF TRANSITION* BY F. VRABEC From the First Eye Clinic, University ofPrague, Czechoslovakia AT the periphery of the cornea the corneal endothelium passes over the margin of Descemet's membrane to the trabecular meshwork (Vrabec, 1957). The size and shape of the cells of the corneal endothelium undergo a peculiar change in approaching this region (Vrabec, 1958a). A study by means of the replica method (Vrabec, 1958b) demonstrated that the endothelial cells became elongated in the meridional direction and then lost their outlines in the region of the anterior border of Schwalbe's ring. Only a few nuclei were seen by the replica technique. The results of examining the endothelium of this zone of transition by various methods is described below. copyright. Material and Methods The eyes of the cat, rabbit, and rhesus monkey were studied, together with some human eyes with different pathological conditions, and one human eye which was clinically niormal but was enucleated because of an orbital tumour. The basic method used was again the silver impregnation method of McGovern (1955, 1956). The results were compared with those obtained by the replica and pseudo-replica methods, the latter mostly with additional staining. Even in the http://bjo.bmj.com/ apparently normal eye, the possibility of functional changes in the secretion of the cement substance as well as of the covering substance should be borne in mind. -
Corneal Endothelium Endothelium Cells Are Destroyed by Disease Or Trauma, Thelial Cells Per Year
Integrating the Best Davis EyeCare Technology Associates Specular Microscopy is a new tech- nique to monitor corneal cell loss due to damage from extended con- tact lens wear, surgery, or the ag- ing process. It is also an excellent tool for: educating patients, screening for corneal disease (fuchs-guttata, kerataconus, Corneal trauma, dry eye, glaucoma, diabe- tes and certain medications etc.) and observing the damaging ef- Endothelium fects of contact lens wear. Often we can avoid more serious complica- tions of con- tact lens wear by under- standing the condition of the cornea. In early stages simply ad- justing the wearing time or chang- ing to a different contact lens ma- terial avoids future issues. In our elderly population our cell counts diminish and with a specular mi- croscope we can monitor and treat Davis EyeCare Associates the aging cornea much more effec- tively. This is an essential tool in managing our contact lens patients 4663 West 95th Street www.daviseyecare.com and is very important in assessing Oak Lawn Il 60453 potential risks for cataracts and Phone: 708-636-0600 4663 West 95th Street refractive surgery. Oak Lawn IL 60453 Fax: 708-636-0606 708-636-0600 E-mail: www.daviseyecare.com mal aging, the central cornea loses 100 to 500 endo- Corneal Endothelium endothelium cells are destroyed by disease or trauma, thelial cells per year. When these cells die, they they are lost forever. slough off the posterior surface of the cornea into the We are pleased to offer Konan Microscopy to the anterior chamber, creating a gap in the endothelial Common ocular conditions, such as glaucoma, uveitis management of your eyecare. -
Notch Signaling Regulates the Differentiation of Neural Crest From
ß 2014. Published by The Company of Biologists Ltd | Journal of Cell Science (2014) 127, 2083–2094 doi:10.1242/jcs.145755 RESEARCH ARTICLE Notch signaling regulates the differentiation of neural crest from human pluripotent stem cells Parinya Noisa1,2, Carina Lund2, Kartiek Kanduri3, Riikka Lund3, Harri La¨hdesma¨ki3, Riitta Lahesmaa3, Karolina Lundin2, Hataiwan Chokechuwattanalert2, Timo Otonkoski4,5, Timo Tuuri5,6,* and Taneli Raivio2,4,*,` ABSTRACT Kokta et al., 2013). Neural crest cells originate from neuroectoderm at the border between the neural plate and the Neural crest cells are specified at the border between the neural epiderm (Meulemans and Bronner-Fraser, 2004), and they are plate and the epiderm. They are capable of differentiating into marked by the expression of genes that are specific for the neural- various somatic cell types, including craniofacial and peripheral plate border, such as DLX5, MSX1, MSX2 and ZIC1. Later, during nerve tissues. Notch signaling plays important roles during the neural-tube folding process, neural crest cells remain within neurogenesis; however, its function during human neural crest the neural folds and subsequently localize inside the dorsal development is poorly understood. Here, we generated self- portion of the neural tube. These premigratory neural crest cells renewing premigratory neural-crest-like cells (pNCCs) from human express specifier genes, such as SNAIL (also known as SNAI1), pluripotent stem cells (hPSCs) and investigated the roles of Notch SLUG (also known as SNAI2), SOX10 and TWIST1 (LaBonne and signaling during neural crest differentiation. pNCCs expressed Bronner-Fraser, 2000; Mancilla and Mayor, 1996). Following the various neural-crest-specifier genes, including SLUG (also known formation of the neural tube, premigratory neural crest cells as SNAI2), SOX10 and TWIST1, and were able to differentiate into undergo an epithelial-to-mesenchymal transition (EMT) and most neural crest derivatives. -
Tissue Engineering of the Corneal Endothelium: a Review of Carrier Materials
J. Funct. Biomater. 2013, 4, 178-208; doi:10.3390/jfb4040178 Journal of Functional Biomaterials ISSN 2079-4983 www.mdpi.com/journal/jfb/ Review Tissue Engineering of the Corneal Endothelium: A Review of Carrier Materials Juliane Teichmann 1,2,†, Monika Valtink 2,†,*, Mirko Nitschke 1, Stefan Gramm 1, Richard H.W. Funk 2,3, Katrin Engelmann 3,4 and Carsten Werner 1,3 1 Leibniz Institute of Polymer Research Dresden, Max Bergmann Center of Biomaterials, Institute of Biofunctional Polymer Materials, Hohe Straße 6, Dresden 01069, Germany; E-Mails: [email protected] (J.T.); [email protected] (M.N.); [email protected] (S.G.); [email protected] (C.W.) 2 Institute of Anatomy, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Fetscherstraße 74, Dresden 01307, Germany; E-Mail: [email protected] 3 CRTD/DFG-Center for Regenerative Therapies Dresden—Cluster of Excellence, Fetscherstraße 105, Dresden 01307, Germany 4 Department of Ophthalmology, Klinikum Chemnitz gGmbH, Flemmingstraße 2, Chemnitz 09116, Germany; E-Mail: [email protected] † These authors contribute equally to the work. * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +49-351-458-6124; Fax: +49-351-458-6303. Received: 3 August 2013; in revised form: 13 September 2013 / Accepted: 24 September 2013 / Published: 22 October 2013 Abstract: Functional impairment of the human corneal endothelium can lead to corneal blindness. In order to meet the high demand for transplants with an appropriate human corneal endothelial cell density as a prerequisite for corneal function, several tissue engineering techniques have been developed to generate transplantable endothelial cell sheets. -
The Migration of Neural Crest Cells and the Growth of Motor Axons Through the Rostral Half of the Chick Somite
/. Embryol. exp. Morph. 90, 437-455 (1985) 437 Printed in Great Britain © The Company of Biologists Limited 1985 The migration of neural crest cells and the growth of motor axons through the rostral half of the chick somite M. RICKMANN, J. W. FAWCETT The Salk Institute and The Clayton Foundation for Research, California division, P.O. Box 85800, San Diego, CA 92138, U.S.A. AND R. J. KEYNES Department of Anatomy, University of Cambridge, Downing St, Cambridge, CB2 3DY, U.K. SUMMARY We have studied the pathway of migration of neural crest cells through the somites of the developing chick embryo, using the monoclonal antibodies NC-1 and HNK-1 to stain them. Crest cells, as they migrate ventrally from the dorsal aspect of the neural tube, pass through the lateral part of the sclerotome, but only through that part of the sclerotome which lies in the rostral half of each somite. This migration pathway is almost identical to the path which pre- sumptive motor axons take when they grow out from the neural tube shortly after the onset of neural crest migration. In order to see whether the ventral root axons are guided along this pathway by neural crest cells, we surgically excised the neural crest from a series of embryos, and examined the pattern of axon outgrowth approximately 24 h later. In somites which contained no neural crest cells, ventral root axons were still found only in the rostral half of the somite, although axonal growth was slightly delayed. These axons were surrounded by sheath cells, which had presumably migrated out of the neural tube, to a point about 50 jan proximal to the growth cones. -
From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal Interactions During Embryonic Development
International Journal of Molecular Sciences Review From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal Interactions during Embryonic Development Nitza Kahane and Chaya Kalcheim * Department of Medical Neurobiology, Institute of Medical Research Israel-Canada (IMRIC) and the Edmond and Lily Safra Center for Brain Sciences (ELSC), Hebrew University of Jerusalem-Hadassah Medical School, P.O. Box 12272, Jerusalem 9112102, Israel; [email protected] * Correspondence: [email protected] Abstract: To ensure the formation of a properly patterned embryo, multiple processes must operate harmoniously at sequential phases of development. This is implemented by mutual interactions between cells and tissues that together regulate the segregation and specification of cells, their growth and morphogenesis. The formation of the spinal cord and paraxial mesoderm derivatives exquisitely illustrate these processes. Following early gastrulation, while the vertebrate body elongates, a pop- ulation of bipotent neuromesodermal progenitors resident in the posterior region of the embryo generate both neural and mesodermal lineages. At later stages, the somitic mesoderm regulates aspects of neural patterning and differentiation of both central and peripheral neural progenitors. Reciprocally, neural precursors influence the paraxial mesoderm to regulate somite-derived myogen- esis and additional processes by distinct mechanisms. Central to this crosstalk is the activity of the axial notochord, which, via sonic hedgehog signaling, plays pivotal roles in neural, skeletal muscle and cartilage ontogeny. Here, we discuss the cellular and molecular basis underlying this complex Citation: Kahane, N.; Kalcheim, C. developmental plan, with a focus on the logic of sonic hedgehog activities in the coordination of the From Bipotent Neuromesodermal Progenitors to Neural-Mesodermal neural-mesodermal axis. -
Pluripotency Factors Regulate Definitive Endoderm Specification Through Eomesodermin
Downloaded from genesdev.cshlp.org on September 23, 2021 - Published by Cold Spring Harbor Laboratory Press Pluripotency factors regulate definitive endoderm specification through eomesodermin Adrian Kee Keong Teo,1,2 Sebastian J. Arnold,3 Matthew W.B. Trotter,1 Stephanie Brown,1 Lay Teng Ang,1 Zhenzhi Chng,1,2 Elizabeth J. Robertson,4 N. Ray Dunn,2,5 and Ludovic Vallier1,5,6 1Laboratory for Regenerative Medicine, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; 2Institute of Medical Biology, A*STAR (Agency for Science, Technology, and Research), Singapore 138648; 3Renal Department, Centre for Clinical Research, University Medical Centre, 79106 Freiburg, Germany; 4Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom Understanding the molecular mechanisms controlling early cell fate decisions in mammals is a major objective toward the development of robust methods for the differentiation of human pluripotent stem cells into clinically relevant cell types. Here, we used human embryonic stem cells and mouse epiblast stem cells to study specification of definitive endoderm in vitro. Using a combination of whole-genome expression and chromatin immunoprecipitation (ChIP) deep sequencing (ChIP-seq) analyses, we established an hierarchy of transcription factors regulating endoderm specification. Importantly, the pluripotency factors NANOG, OCT4, and SOX2 have an essential function in this network by actively directing differentiation. Indeed, these transcription factors control the expression of EOMESODERMIN (EOMES), which marks the onset of endoderm specification. In turn, EOMES interacts with SMAD2/3 to initiate the transcriptional network governing endoderm formation. Together, these results provide for the first time a comprehensive molecular model connecting the transition from pluripotency to endoderm specification during mammalian development. -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal.