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The Genetic Basis of Mammalian Neurulation
REVIEWS THE GENETIC BASIS OF MAMMALIAN NEURULATION Andrew J. Copp*, Nicholas D. E. Greene* and Jennifer N. Murdoch‡ More than 80 mutant mouse genes disrupt neurulation and allow an in-depth analysis of the underlying developmental mechanisms. Although many of the genetic mutants have been studied in only rudimentary detail, several molecular pathways can already be identified as crucial for normal neurulation. These include the planar cell-polarity pathway, which is required for the initiation of neural tube closure, and the sonic hedgehog signalling pathway that regulates neural plate bending. Mutant mice also offer an opportunity to unravel the mechanisms by which folic acid prevents neural tube defects, and to develop new therapies for folate-resistant defects. 6 ECTODERM Neurulation is a fundamental event of embryogenesis distinct locations in the brain and spinal cord .By The outer of the three that culminates in the formation of the neural tube, contrast, the mechanisms that underlie the forma- embryonic (germ) layers that which is the precursor of the brain and spinal cord. A tion, elevation and fusion of the neural folds have gives rise to the entire central region of specialized dorsal ECTODERM, the neural plate, remained elusive. nervous system, plus other organs and embryonic develops bilateral neural folds at its junction with sur- An opportunity has now arisen for an incisive analy- structures. face (non-neural) ectoderm. These folds elevate, come sis of neurulation mechanisms using the growing battery into contact (appose) in the midline and fuse to create of genetically targeted and other mutant mouse strains NEURAL CREST the neural tube, which, thereafter, becomes covered by in which NTDs form part of the mutant phenotype7.At A migratory cell population that future epidermal ectoderm. -
Clonal Dispersion During Neural Tube Formation 4097 of Neuromeres
Development 126, 4095-4106 (1999) 4095 Printed in Great Britain © The Company of Biologists Limited 1999 DEV2458 Successive patterns of clonal cell dispersion in relation to neuromeric subdivision in the mouse neuroepithelium Luc Mathis1,*, Johan Sieur1, Octavian Voiculescu2, Patrick Charnay2 and Jean-François Nicolas1,‡ 1Unité de Biologie moléculaire du Développement, Institut Pasteur, 25, rue du Docteur Roux, 75724 Paris Cedex 15, France 2Unité INSERM 368, Ecole Normale Supérieure, 46 rue d’Ulm, 75230 Paris Cedex 05, France *Present address: Beckman Institute (139-74), California Institute of Technology, Pasadena, CA, 91125, USA ‡Author for correspondence (e-mail: [email protected]) Accepted 5 July; published on WWW 23 August 1999 SUMMARY We made use of the laacz procedure of single-cell labelling the AP and DV axis of the neural tube. A similar sequence to visualize clones labelled before neuromere formation, in of AP cell dispersion followed by an arrest of AP cell 12.5-day mouse embryos. This allowed us to deduce two dispersion, a preferential DV cell dispersion and then by a successive phases of cell dispersion in the formation of the coherent neuroepithelial growth, is also observed in the rhombencephalon: an initial anterior-posterior (AP) cell spinal cord and mesencephalon. This demonstrates that a dispersion, followed by an asymmetrical dorsoventral (DV) similar cascade of cell events occurs in these different cell distribution during which AP cell dispersion occurs in domains of the CNS. In the prosencephalon, differences in territories smaller than one rhombomere. We conclude that spatial constraints may explain the variability in the the general arrest of AP cell dispersion precedes the onset orientation of cell clusters. -
Fetal Brain Anomalies Associated with Ventriculomegaly Or Asymmetry: an MRI-Based Study
ORIGINAL RESEARCH PEDIATRICS Fetal Brain Anomalies Associated with Ventriculomegaly or Asymmetry: An MRI-Based Study X E. Barzilay, X O. Bar-Yosef, X S. Dorembus, X R. Achiron, and X E. Katorza ABSTRACT BACKGROUND AND PURPOSE: Fetal lateral ventriculomegaly is a relatively common finding with much debate over its clinical signifi- cance. The purpose of this study was to examine the association between ventriculomegaly and asymmetry and concomitant CNS findings as seen in fetal brain MR imaging. MATERIALS AND METHODS: Fetal brain MR imaging performed for various indications, including ventriculomegaly, with or without additional ultrasound findings, was assessed for possible inclusion. Two hundred seventy-eight cases found to have at least 1 lateral ventricle with a width of Ն10 mm were included in the study. Ventriculomegaly was considered mild if the measurement was 10–11.9 mm; moderate if, 12–14.9 mm; and severe if, Ն15 mm. Asymmetry was defined as a difference of Ն2 mm between the 2 lateral ventricles. Fetal brain MR imaging findings were classified according to severity by predefined categories. RESULTS: The risk of CNS findings appears to be strongly related to the width of the ventricle (OR, 1.38; 95% CI, 1.08–1.76; P ϭ .009). The prevalence of associated CNS abnormalities was significantly higher (P ϭ .005) in symmetric ventriculomegaly compared with asymmetric ventriculomegaly (38.8% versus 24.2%, respectively, for all CNS abnormalities and 20% versus 7.1%, respectively, for major CNS abnormalities). CONCLUSIONS: In this study, we demonstrate that the rate of minor and major findings increased with each millimeter increase in ventricle width and that the presence of symmetric ventricles in mild and moderate ventriculomegaly was a prognostic indicator for CNS abnormalities. -
Mir-124 Regulates Early Neurogenesis in the Optic Vesicle and Forebrain, Targeting Neurod1
Published online 3 December 2010 Nucleic Acids Research, 2011, Vol. 39, No. 7 2869–2879 doi:10.1093/nar/gkq904 MiR-124 regulates early neurogenesis in the optic vesicle and forebrain, targeting NeuroD1 Kaili Liu1,2,3, Ying Liu1,2,*, Weichuan Mo1,3, Rong Qiu1, Xiumei Wang1,2, Jane Y. Wu1,4 and Rongqiao He1,3,5,* 1The State Key Laboratory of Brain and Cognitive Science, 2Key Laboratory of Noncoding RNA, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Chaoyang District, Beijing 100101, 3Graduate University of Chinese Academy of Sciences, Beijing 100049, China, 4Department of Neurology, Lurie Comprehensive Cancer Center, Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA and 5Key Laboratory of Mental Health, Chinese Academy of Sciences, Beijing 100101, China Received April 23, 2010; Revised September 5, 2010; Accepted September 23, 2010 ABSTRACT post-transcriptional mechanisms controlling their expres- sion are poorly understood. In recent years, systematic MicroRNAs (miRNAs) are involved in the fine control studies in zebrafish and mouse have determined specific of cell proliferation and differentiation during the microRNAs (miRNAs) expressed in the developing eye development of the nervous system. MiR-124, a and brain (1,2). MiR-7 and let-7 have been shown to be neural specific miRNA, is expressed from the begin- involved in Drosophila eye development (3,4). In Xenopus, ning of eye development in Xenopus, and has been miR-24a has been reported to play an essential role in shown to repress cell proliferation in the optic cup, repressing apoptosis in the developing neural retina (5). -
Differentiation of the Cerebellum 2463
Development 128, 2461-2469 (2001) 2461 Printed in Great Britain © The Company of Biologists Limited 2001 DEV1660 Inductive signal and tissue responsiveness defining the tectum and the cerebellum Tatsuya Sato, Isato Araki‡ and Harukazu Nakamura* Department of Molecular Neurobiology, Institute of Development, Aging and Cancer, Seiryo-machi 4-1, Aoba-ku, Sendai 980- 8575, Japan ‡Present address: Department of Neurobiology, University of Heidelberg, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany *Author for correspondence (e-mail: [email protected]) Accepted 11 April 2001 SUMMARY The mes/metencephalic boundary (isthmus) has an Fgf8b repressed Otx2 expression, but upregulated Gbx2 and organizing activity for mesencephalon and metencephalon. Irx2 expression in the mesencephalon. As a result, Fgf8b The candidate signaling molecule is Fgf8 whose mRNA is completely changed the fate of the mesencephalic alar plate localized in the region where the cerebellum differentiates. to cerebellum. Quantitative analysis showed that Fgf8b Responding to this signal, the cerebellum differentiates in signal is 100 times stronger than Fgf8a signal. Co- the metencephalon and the tectum differentiates in the transfection of Fgf8b with Otx2 indicates that Otx2 is a key mesencephalon. Based on the assumption that strong Fgf8 molecule in mesencephalic generation. We have shown by signal induces the cerebellum and that the Fgf8b signal is RT-PCR that both Fgf8a and Fgf8b are expressed, Fgf8b stronger than that of Fgf8a, we carried out experiments to expression prevailing in the isthmic region. The results all misexpress Fgf8b and Fgf8a in chick embryos. Fgf8a did not support our working hypothesis that the strong Fgf8 signal affect the expression pattern of Otx2, Gbx2 or Irx2. -
NERVOUS SYSTEM هذا الملف لالستزادة واثراء المعلومات Neuropsychiatry Block
NERVOUS SYSTEM هذا الملف لﻻستزادة واثراء المعلومات Neuropsychiatry block. قال تعالى: ) َو َل َق د َخ َل قنَا ا ِْلن َسا َن ِمن ُس ََل َل ة ِ من ِطي ن }12{ ثُ م َجعَ لنَاه ُ نُ ط َفة فِي َق َرا ر م ِكي ن }13{ ثُ م َخ َل قنَا ال ُّن ط َفة َ َع َل َقة َف َخ َل قنَا ا لعَ َل َقة َ ُم ضغَة َف َخ َل قنَا ا ل ُم ضغَة َ ِع َظا ما َف َك َس ونَا ا ل ِع َظا َم َل ح ما ثُ م أَن َشأنَاه ُ َخ ل قا آ َخ َر َفتَبَا َر َك ّللا ُ أَ ح َس ُن ا ل َخا ِل ِقي َن }14{( Resources BRS Embryology Book. Pathoma Book ( IN DEVELOPMENTAL ANOMALIES PART ). [email protected] 1 OVERVIEW A- Central nervous system (CNS) is formed in week 3 of development, during which time the neural plate develops. The neural plate, consisting of neuroectoderm, becomes the neural tube, which gives rise to the brain and spinal cord. B- Peripheral nervous system (PNS) is derived from three sources: 1. Neural crest cells 2. Neural tube, which gives rise to all preganglionic autonomic nerves (sympathetic and parasympathetic) and all nerves (-motoneurons and -motoneurons) that innervate skeletal muscles 3. Mesoderm, which gives rise to the dura mater and to connective tissue investments of peripheral nerve fibers (endoneurium, perineurium, and epineurium) DEVELOPMENT OF THE NEURAL TUBE Neurulation refers to the formation and closure of the neural tube. BMP-4 (bone morphogenetic protein), noggin (an inductor protein), chordin (an inductor protein), FGF-8 (fibroblast growth factor), and N-CAM (neural cell adhesion molecule) appear to play a role in neurulation. -
Locus Coeruleus Complex of the Family Delphinidae
www.nature.com/scientificreports OPEN Locus coeruleus complex of the family Delphinidae Simona Sacchini 1, Manuel Arbelo 1, Cristiano Bombardi2, Antonio Fernández1, Bruno Cozzi 3, Yara Bernaldo de Quirós1 & Pedro Herráez1 Received: 19 July 2017 The locus coeruleus (LC) is the largest catecholaminergic nucleus and extensively projects to widespread Accepted: 22 March 2018 areas of the brain and spinal cord. The LC is the largest source of noradrenaline in the brain. To date, the Published: xx xx xxxx only examined Delphinidae species for the LC has been a bottlenose dolphin (Tursiops truncatus). In our experimental series including diferent Delphinidae species, the LC was composed of fve subdivisions: A6d, A6v, A7, A5, and A4. The examined animals had the A4 subdivision, which had not been previously described in the only Delphinidae in which this nucleus was investigated. Moreover, the neurons had a large amount of neuromelanin in the interior of their perikarya, making this nucleus highly similar to that of humans and non-human primates. This report also presents the frst description of neuromelanin in the cetaceans’ LC complex, as well as in the cetaceans’ brain. Te locus coeruleus (LC) is a densely packed cluster of noradrenaline-producing neurons located in the upper part of the rostral rhombencephalon, on the lateral edge of the fourth ventricle. Te LC is the largest catechola- minergic nucleus of the brain, and it supplies noradrenaline to the entire central nervous system. Noradrenaline neurons are located in the medulla oblongata and pons (termed A1-A7 divisions), while adrenaline neurons are located only in the medulla oblongata, near A1-A3 (and termed C1-C3)1. -
And Krox-20 and on Morphological Segmentation in the Hindbrain of Mouse Embryos
The EMBO Journal vol.10 no.10 pp.2985-2995, 1991 Effects of retinoic acid excess on expression of Hox-2.9 and Krox-20 and on morphological segmentation in the hindbrain of mouse embryos G.M.Morriss-Kay, P.Murphy1,2, R.E.Hill1 and in embryos are unknown, but in human embryonal D.R.Davidson' carcinoma cells they include the nine genes of the Hox-2 cluster (Simeone et al., 1990). Department of Human Anatomy, South Parks Road, Oxford OXI 3QX The hindbrain and the neural crest cells derived from it and 'MRC Human Genetics Unit, Western General Hospital, Crewe are of particular interest in relation to the developmental Road, Edinburgh EH4 2XU, UK functions of RA because they are abnormal in rodent 2Present address: Istituto di Istologia ed Embriologia Generale, embryos exposed to a retinoid excess during or shortly before Universita di Roma 'la Sapienza', Via A.Scarpa 14, 00161 Roma, early neurulation stages of development (Morriss, 1972; Italy Morriss and Thorogood, 1978; Webster et al., 1986). Communicated by P.Chambon Human infants exposed to a retinoid excess in utero at early developmental stages likewise show abnormalities of the Mouse embryos were exposed to maternally administered brain and of structures to which cranial neural crest cells RA on day 8.0 or day 73/4 of development, i.e. at or just contribute (Lammer et al., 1985). Retinoid-induced before the differentiation of the cranial neural plate, and abnormalities of hindbrain morphology in rodent embryos before the start of segmentation. On day 9.0, the RA- include shortening of the preotic region in relation to other treated embryos had a shorter preotic hindbrain than the head structures, so that the otocyst lies level with the first controls and clear rhombomeric segmentation was pharyngeal arch instead of the second (Morriss, 1972; absent. -
How Does the Human Brain Differentiate? —Normal and Abnormal Development—
Forum Forma, 27, S29–S31, 2012 How does the Human Brain Differentiate? —Normal and Abnormal Development— Yoshihiro Fukui Department of Anatomy and Developmental Neurobiology, University of Tokushima Graduate School, Institute of Health Biosciences, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan E-mail address: [email protected] (Received January 24, 2012; Accepted March 17, 2012) Keywords: Neural Tube, Brain Vesicle, Cerebrospinal Fluid, Hydrocephalus, Anencephaly, Microcephaly 1. Three Primary Brain Vesicles Convert into Five Sec- 2. Development of the Brain Ventricular System ondary Brain Vesicles The expanded primitive ventricles formed by the neural The central nervous system (CNS) appears during the 3rd canal in the secondary brain vesicles give rise to the ven- week as a neural plate growing out from the ectoderm of tricular system of the brain (Fig. 2). The ventricles of the the germ disc. The lateral edges elevate to form the neural brain include the lateral, third, and fourth ventricles. The folds, and finally fuse, forming the neural tube. Neurula- two lateral ventricles communicate through the interven- tion begins on day 22, and the cranial neuropore, which is tricular foramina (of Monro) with the third ventricle. The an opening at anterior end of the embryonic neural canal, third ventricle is connected to the fourth ventricle by the closes on day 24. The future eyes appear as outpouchings cerebral aqueduct (aqueduct of Sylvius). The fourth ven- from the forebrain neural folds by day 22. Before neu- tricle in turn is continuous with the narrow central canal of rulation begins, the primordia of the three primary brain the spinal cord and, through the three foramina in its roof, vesicles are visible as broadenings in the neural plate as with the subarachnoid space. -
Neuroanatomy Dr
Neuroanatomy Dr. Maha ELBeltagy Assistant Professor of Anatomy Faculty of Medicine The University of Jordan 2018 Prof Yousry 10/15/17 A F B K G C H D I M E N J L Ventricular System, The Cerebrospinal Fluid, and the Blood Brain Barrier The lateral ventricle Interventricular foramen It is Y-shaped cavity in the cerebral hemisphere with the following parts: trigone 1) A central part (body): Extends from the interventricular foramen to the splenium of corpus callosum. 2) 3 horns: - Anterior horn: Lies in the frontal lobe in front of the interventricular foramen. - Posterior horn : Lies in the occipital lobe. - Inferior horn : Lies in the temporal lobe. rd It is connected to the 3 ventricle by body interventricular foramen (of Monro). Anterior Trigone (atrium): the part of the body at the horn junction of inferior and posterior horns Contains the glomus (choroid plexus tuft) calcified in adult (x-ray&CT). Interventricular foramen Relations of Body of the lateral ventricle Roof : body of the Corpus callosum Floor: body of Caudate Nucleus and body of the thalamus. Stria terminalis between thalamus and caudate. (connects between amygdala and venteral nucleus of the hypothalmus) Medial wall: Septum Pellucidum Body of the fornix (choroid fissure between fornix and thalamus (choroid plexus) Relations of lateral ventricle body Anterior horn Choroid fissure Relations of Anterior horn of the lateral ventricle Roof : genu of the Corpus callosum Floor: Head of Caudate Nucleus Medial wall: Rostrum of corpus callosum Septum Pellucidum Anterior column of the fornix Relations of Posterior horn of the lateral ventricle •Roof and lateral wall Tapetum of the corpus callosum Optic radiation lying against the tapetum in the lateral wall. -
Cephalic Neurulation in the Mouse Embryo Analyzed by SEM and Morphometry
THE ANATOMICAL RECORD 203:375-396 (1982) Cephalic Neurulation in the Mouse Embryo Analyzed by SEM and Morphometry ANTONE G. JACOBSON AND PATRICK P.L. TAM Department of Zoology. Uniuersity of Texas, Austin, TX 78712 (A.G.J.) and Department of Anatomy, (‘hinese University of Hong Kong, Shatin, N.T., Hong Kong IP.PL.T) ABSTRACT A detailed account of mouse neurulation is given based mostly on SEM analysis over 20 hr of development. Many observations and measure- ments were made on staged living embryos and on embryos prepared for scanning and light microscopy to help deduce what mechanisms may contribute to neural tube formation. Each lateral half of the early cephalic neural plate makes a convex bulge, opposite to the way it must fold to form a tube. Underlying mesenchyme and matrix are reported to have a role in forming these bulges. Processes that form the tube must overcome this opposed folding and the forces that produce it. Crani- al flexure begins long before tube formation. The flexure commences at the rostra1 tip of the cephalic neural plate, then the apex of the flexure migrates caudally to the mesencephalic region. Early appearance of this flexure imposes a mechanical impediment to tube closure in forebrain and midbrain regions. Tube closure begins in the cervical region exactly where the neural plate is reflected dorsally by a bend in the embryo. This bend may mechanically assist closure in this region. Cells of the mouse neural plate are reported to contain organized microfilaments and mi- crotubules, and the plate cells appear to change shape (reduce apical area and in- crease cell height) in the same manner as that suggested in embryos of some other species to contribute to neural tube formation. -
Neuroanatomy
Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Neuroanatomy W. Jeffrey Wilson Fall 2012 \Without education we are in a horrible and deadly danger of taking educated people seriously." { Gilbert Keith Chesterton [LATEX in use { a Microsoft- & PowerPoint-free presentation] Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Blood-Brain Barrier Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Peripheral Nervous System • Somatic N.S.: skeletal muscles, skin, joints • Autonomic N.S.: internal organs, glands • Sympathetic N.S.: rapid expenditure of energy • Parasympathetic N.S.: restoration of energy Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Spinal Cord Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain | Ventricles Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain Midline Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain Midline Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Hindbrain Myelencephalon & Metencephalon Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Reticular