Cells of the Spinal Cord. Rexed Zones. Spinal Reflexes. Receptors and Effectors
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NS201C Anatomy 1: Sensory and Motor Systems
NS201C Anatomy 1: Sensory and Motor Systems 25th January 2017 Peter Ohara Department of Anatomy [email protected] The Subdivisions and Components of the Central Nervous System Axes and Anatomical Planes of Sections of the Human and Rat Brain Development of the neural tube 1 Dorsal and ventral cell groups Dermatomes and myotomes Neural crest derivatives: 1 Neural crest derivatives: 2 Development of the neural tube 2 Timing of development of the neural tube and its derivatives Timing of development of the neural tube and its derivatives Gestational Crown-rump Structure(s) age (Weeks) length (mm) 3 3 cerebral vesicles 4 4 Optic cup, otic placode (future internal ear) 5 6 cerebral vesicles, cranial nerve nuclei 6 12 Cranial and cervical flexures, rhombic lips (future cerebellum) 7 17 Thalamus, hypothalamus, internal capsule, basal ganglia Hippocampus, fornix, olfactory bulb, longitudinal fissure that 8 30 separates the hemispheres 10 53 First callosal fibers cross the midline, early cerebellum 12 80 Major expansion of the cerebral cortex 16 134 Olfactory connections established 20 185 Gyral and sulcul patterns of the cerebral cortex established Clinical case A 68 year old woman with hypertension and diabetes develops abrupt onset numbness and tingling on the right half of the face and head and the entire right hemitrunk, right arm and right leg. She does not experience any weakness or incoordination. Physical Examination: Vitals: T 37.0° C; BP 168/87; P 86; RR 16 Cardiovascular, pulmonary, and abdominal exam are within normal limits. Neurological Examination: Mental Status: Alert and oriented x 3, 3/3 recall in 3 minutes, language fluent. -
Deconstructing Spinal Interneurons, One Cell Type at a Time Mariano Ignacio Gabitto
Deconstructing spinal interneurons, one cell type at a time Mariano Ignacio Gabitto Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy under the Executive Committee of the Graduate School of Arts and Sciences COLUMBIA UNIVERSITY 2016 © 2016 Mariano Ignacio Gabitto All rights reserved ABSTRACT Deconstructing spinal interneurons, one cell type at a time Mariano Ignacio Gabitto Abstract Documenting the extent of cellular diversity is a critical step in defining the functional organization of the nervous system. In this context, we sought to develop statistical methods capable of revealing underlying cellular diversity given incomplete data sampling - a common problem in biological systems, where complete descriptions of cellular characteristics are rarely available. We devised a sparse Bayesian framework that infers cell type diversity from partial or incomplete transcription factor expression data. This framework appropriately handles estimation uncertainty, can incorporate multiple cellular characteristics, and can be used to optimize experimental design. We applied this framework to characterize a cardinal inhibitory population in the spinal cord. Animals generate movement by engaging spinal circuits that direct precise sequences of muscle contraction, but the identity and organizational logic of local interneurons that lie at the core of these circuits remain unresolved. By using our Sparse Bayesian approach, we showed that V1 interneurons, a major inhibitory population that controls motor output, fractionate into diverse subsets on the basis of the expression of nineteen transcription factors. Transcriptionally defined subsets exhibit highly structured spatial distributions with mediolateral and dorsoventral positional biases. These distinctions in settling position are largely predictive of patterns of input from sensory and motor neurons, arguing that settling position is a determinant of inhibitory microcircuit organization. -
Delineating the Diversity of Spinal Interneurons in Locomotor Circuits
The Journal of Neuroscience, November 8, 2017 • 37(45):10835–10841 • 10835 Mini-Symposium Delineating the Diversity of Spinal Interneurons in Locomotor Circuits Simon Gosgnach,1 Jay B. Bikoff,2 XKimberly J. Dougherty,3 Abdeljabbar El Manira,4 XGuillermo M. Lanuza,5 and Ying Zhang6 1Department of Physiology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada, 2Department of Neuroscience, Columbia University, New York, New York 10032, 3Department of Neurobiology and Anatomy, Drexel University, Philadelphia, Pennsylvania 19129, 4Department of Neuroscience, Karolinska Institutet, Stockholm SE-171 77, Sweden, 5Department of Developmental Neurobiology, Fundacion Instituto Leloir, Buenos Aires C1405BWE, Argentina, and 6Department of Medical Neuroscience, Dalhousie University. Halifax, Nova Scotia B3H 4R2, Canada Locomotion is common to all animals and is essential for survival. Neural circuits located in the spinal cord have been shown to be necessary and sufficient for the generation and control of the basic locomotor rhythm by activating muscles on either side of the body in a specific sequence. Activity in these neural circuits determines the speed, gait pattern, and direction of movement, so the specific locomotor pattern generated relies on the diversity of the neurons within spinal locomotor circuits. Here, we review findings demon- strating that developmental genetics can be used to identify populations of neurons that comprise these circuits and focus on recent work indicating that many of these populations can be further subdivided -
The Spinal Cord Is a Nerve Column That Passes Downward from Brain Into the Vertebral Canal
The spinal cord is a nerve column that passes downward from brain into the vertebral canal. Recall that it is part of the CNS. Spinal nerves extend to/from the spinal cord and are part of the PNS. Length = about 17 inches Start = foramen magnum End = tapers to point (conus medullaris) st nd and terminates 1 –2 lumbar (L1-L2) vertebra Contains 31 segments à gives rise to 31 pairs of spinal nerves Note cervical and lumbar enlargements. cauda equina (“horse’s tail”) –collection of spinal nerves at inferior end of vertebral column (nerves coming off end of spinal cord) Meninges- cushion and protected by same 3 layers as brain. Extend past end of cord into vertebral canal à spinal tap because no cord A cross-section of the spinal cord resembles a butterfly with its wings outspread (gray matter) surrounded by white matter. GRAY MATTER or “butterfly” = bundles of cell bodies Posterior (dorsal) horns=association or interneurons (incoming somatosensory information) Lateral horns=autonomic neurons Anterior (ventral) horns=cell bodies of motor neurons Central canal-found within gray matter and filled with CSF White Matter: 3 Regions: Posterior (dorsal) white column or funiculi – contains only ASCENDING tracts à sensory only Lateral white column or funiculi – both ascending and descending tracts à sensory and motor Anterior (ventral) white column or funiculi – both ascending and descending tracts à sensory and motor All nerve tracts made of mylinated axons with same destination and function Associated Structures: Dorsal Roots = made -
Spinal Cord Organization
Lecture 4 Spinal Cord Organization The spinal cord . Afferent tract • connects with spinal nerves, through afferent BRAIN neuron & efferent axons in spinal roots; reflex receptor interneuron • communicates with the brain, by means of cell ascending and descending pathways that body form tracts in spinal white matter; and white matter muscle • gives rise to spinal reflexes, pre-determined gray matter Efferent neuron by interneuronal circuits. Spinal Cord Section Gross anatomy of the spinal cord: The spinal cord is a cylinder of CNS. The spinal cord exhibits subtle cervical and lumbar (lumbosacral) enlargements produced by extra neurons in segments that innervate limbs. The region of spinal cord caudal to the lumbar enlargement is conus medullaris. Caudal to this, a terminal filament of (nonfunctional) glial tissue extends into the tail. terminal filament lumbar enlargement conus medullaris cervical enlargement A spinal cord segment = a portion of spinal cord that spinal ganglion gives rise to a pair (right & left) of spinal nerves. Each spinal dorsal nerve is attached to the spinal cord by means of dorsal and spinal ventral roots composed of rootlets. Spinal segments, spinal root (rootlets) nerve roots, and spinal nerves are all identified numerically by th region, e.g., 6 cervical (C6) spinal segment. ventral Sacral and caudal spinal roots (surrounding the conus root medullaris and terminal filament and streaming caudally to (rootlets) reach corresponding intervertebral foramina) collectively constitute the cauda equina. Both the spinal cord (CNS) and spinal roots (PNS) are enveloped by meninges within the vertebral canal. Spinal nerves (which are formed in intervertebral foramina) are covered by connective tissue (epineurium, perineurium, & endoneurium) rather than meninges. -
Review of Spinal Cord Basics of Neuroanatomy Brain Meninges
Review of Spinal Cord with Basics of Neuroanatomy Brain Meninges Prof. D.H. Pauža Parts of Nervous System Review of Spinal Cord with Basics of Neuroanatomy Brain Meninges Prof. D.H. Pauža Neurons and Neuroglia Neuron Human brain contains per 1011-12 (trillions) neurons Body (soma) Perikaryon Nissl substance or Tigroid Dendrites Axon Myelin Terminals Synapses Neuronal types Unipolar, pseudounipolar, bipolar, multipolar Afferent (sensory, centripetal) Efferent (motor, centrifugal, effector) Associate (interneurons) Synapse Presynaptic membrane Postsynaptic membrane, receptors Synaptic cleft Synaptic vesicles, neuromediator Mitochondria In human brain – neurons 1011 (100 trillions) Synapses – 1015 (quadrillions) Neuromediators •Acetylcholine •Noradrenaline •Serotonin •GABA •Endorphin •Encephalin •P substance •Neuronal nitric oxide Adrenergic nerve ending. There are many 50-nm-diameter vesicles (arrow) with dark, electron-dense cores containing norepinephrine. x40,000. Cell Types of Neuroglia Astrocytes - Oligodendrocytes – Ependimocytes - Microglia Astrocytes – a part of hemoencephalic barrier Oligodendrocytes Ependimocytes and microglial cells Microglia represent the endogenous brain defense and immune system, which is responsible for CNS protection against various types of pathogenic factors. After invading the CNS, microglial precursors disseminate relatively homogeneously throughout the neural tissue and acquire a specific phenotype, which clearly distinguish them from their precursors, the blood-derived monocytes. The ´resting´ microglia -
Neuropathology of the Brainstem and Spinal Cord in End Stage Rheumatoid Arthritis: Implications for Treatment
Annals of the Rheumatic Diseases 1993; 52: 629-637 629 EXTENDED REPORTS Ann Rheum Dis: first published as 10.1136/ard.52.9.629 on 1 September 1993. Downloaded from Neuropathology of the brainstem and spinal cord in end stage rheumatoid arthritis: implications for treatment Fraser C Henderson, Jennian F Geddes, H Alan Crockard Abstract Methods Objective-To study the detailed histo- This study includes nine patients with sero- pathological changes in the brainstem and positive rheumatoid arthritis (eight women, spinal cord in nine patients with severe one man) from our ongoing prospective study, end stage rheumatoid arthritis, all with who underwent necropsy at the National clinical myelopathy and craniocervical Hospitals for Neurology and Neurosurgery compression. between 1987 and 1991. All patients were Methods-At necropsy the sites of bony evaluated by rheumatologists, a neurosurgeon pathology were related exactly to cord (HAC), two neuroradiologists, a physio- segments and histological changes, and therapist, and a research nurse. The clinical correlated with clinical and radiological assessment included a full neurological exam- findings. ination and a detailed questionnaire about Results-Cranial nerve and brainstem neurological symptoms. In addition, all pathology was rare. In addition to the patients were graded according to Ranawat obvious craniocervical compression, there et al'9 and Steinbrocker et al.20 The radiological were widespread subaxial changes in assessment included plain lateral films of the the spinal cord. Pathology was localised cervical spine and high definition computed primarily to the dorsal white matter and myelotomography with multiplanar refor- there was no evidence of vasculitis or matting.2' All operations were carried out by or ischaemic changes. -
Theory on How Syrinxes Form
Theories | 02.04 Key Points New Theory On How Syrinxes Form 1. Mathematical model, or Many theories on syrinx formation have come and gone over the years. While they vary in their details, most analysis, of the CSF system in modern theories focus on the dynamics of how CSF flows and under what conditions it would create a syrinx. Chiari and syringomyelia was Cerebrospinal fluid bathes the brain and spinal cord and acts as a protective cushion and shock absorber. In a created healthy person, CSF flows freely from the brain to the spinal region (around the cerebellar tonsils) and back again in concert with a person's heartbeat. When the cerebellar tonsils descend out of the skull and crowd the 2. It models the system as two, spinal cord, one of the main passages for this CSF can be blocked. For decades now, doctors and scientists co-axial tubes filled with fluid have been trying to understand how this blockage can lead to a syrinx forming in the spinal cord.. (CSF) Gardner kicked it all off with a theory that stated if a Chiari malformation blocks the natural flow of CSF out of the 3. New theory says that during a brain, it will be redirected and flow down the central canal of the spinal cord instead and create a syrinx. This cough or sneeze, a pressure theory may work for a subset of cases, but it has since been shown that in most adults, the central canal closes wave travels up the spine and off and would not allow this type of CSF flow. -
MENINGES and CEREBROSPINAL FLUID' by LEWIS H
MENINGES AND CEREBROSPINAL FLUID' By LEWIS H. WEED Department of Anatomy, John Hopkins University THE divorce of structure from function is particularly difficult in any ana- tomical study: it was only 85 years ago that the two subjects of morphology and physiology were considered to justify separate departments as academic disciplines. But with this cleavage which fortunately has not at any time been a rigid one, only certain investigations could go forward without loss of in- spiration and interpretation when studied apart from the sister science; other researches were enormously hampered and could be attacked only with due regard to structure and function. So it is without apologies that I begin the presentation of the problem of the coverings of the central nervous system -coverings which encompass a characteristic body fluid. Here then is a problem of membranes serving to contain a clear, limpid liquid as a sac might hold it. Immediately many questions of biological significance are at hand: how does it happen that these structures retain fluid; where does the fluid come from; where does it go; is the fluid constantly produced or is it an inert, non-circu- lating medium; is the fluid under pressure above that of the atmosphere; does it move about with changes in the animal body?-but the list of problems springing into one's mind grows too long. Knowledge regarding these many questions has progressed since the first accounts of hydrocephalus were given by writers in the Hippocratic corpus, since discovery of the normal ventricular fluid in Galen's time, since its meningeal existence was first uncovered by Valsalva (1911) and advanced by Cotugno (1779), since the first adequate description by Magendie (1825) 100 years ago. -
Evoked Spinal Cord Potentials.Pdf
EVPPR 11/29/05 12:39 PM Page I K. Shimoji, W.D. Willis, Jr. (Eds.) Evoked Spinal Cord Potentials An Illustrated Guide to Physiology, Pharmacology, and Recording Techniques EVPPR 11/29/05 12:39 PM Page III K. Shimoji, W.D. Willis, Jr. (Eds.) Evoked Spinal Cord Potentials An Illustrated Guide to Physiology, Pharmacology, and Recording Techniques With 130 Figures EVPPR 11/30/05 10:06 AM Page IV Editors: Koki Shimoji, M.D., Ph.D., FRCA Professor, Frontier University Ube Graduate School of Human Sciences 2-1-1 Bunkyodai, Ube, Yamaguchi 755-0805,Japan Professor Emeritus, Niigata University Visiting Professor, Saitama Medical College William D. Willis, Jr., M.D., Ph.D. Professor of Neuroscience and Cell Biology University of Texas Medical Branch 301 University Blvd., Galveston, TX 77555-1069, USA Authors: Tatsuhiko Kano, M.D., Ph.D. Professor and Chairman Department of Anesthesiology Kurume University School of Medicine Yoichi Katayama, M.D., Ph.D. Professor and Chairman Department of Neurosurgery Nihon University School of Medicine Satoru Fukuda, M.D., Ph.D. Professor and Chairman Department of Anesthesiology and Reanimation Fukui University School of Medicine Library of Congress Control Number: 2005935847 ISBN-10 4-431-24026-8 Springer-Verlag Tokyo Berlin Heidelberg New York ISBN-13 978-4-431-24026-6 Springer-Verlag Tokyo Berlin Heidelberg New York This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broad- casting, reproduction on microfilms or in other ways, and storage in data banks. -
Wnt/Β-Catenin Signaling Regulates Ependymal Cell Development and Adult Homeostasis
Wnt/β-catenin signaling regulates ependymal cell development and adult homeostasis Liujing Xinga, Teni Anbarchiana, Jonathan M. Tsaia, Giles W. Plantb, and Roeland Nussea,c,1 aDepartment of Developmental Biology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305; bDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305; and cHoward Hughes Medical Institute, Stanford, CA 94305 Contributed by Roeland Nusse, May 22, 2018 (sent for review February 23, 2018; reviewed by Bin Chen and Samuel Pleasure) In the adult mouse spinal cord, the ependymal cell population that precursors and are present before the onset of neurogenesis. surrounds the central canal is thought to be a promising source of They give rise to radial glial cells, which then become the pre- quiescent stem cells to treat spinal cord injury. Relatively little is dominant progenitors during gliogenesis (19, 20). Eventually, known about the cellular origin of ependymal cells during spinal ependymal cells are formed as the ventricle and the ventricular cord development, or the molecular mechanisms that regulate zone retract through the process of obliteration. This process is ependymal cells during adult homeostasis. Using genetic lineage accompanied by terminal differentiation and exit of radial glial tracing based on the Wnt target gene Axin2, we have character- cells from the ventricular zone (18, 19, 21–24). ized Wnt-responsive cells during spinal cord development. Our Compared with our knowledge about ependymal cells in the results revealed that Wnt-responsive progenitor cells are restricted brain, little is known about the cellular origin of spinal cord to the dorsal midline throughout spinal cord development, which ependymal cells. -
Correlation of Diffusion Tensor Imaging Indices with Histological
Marquette University e-Publications@Marquette Master's Theses (2009 -) Dissertations, Theses, and Professional Projects Correlation of Diffusion Tensor Imaging Indices with Histological Parameters in Rat Cervical Spinal Cord Gray Matter Following Distal Contusion Spinal Cord Injury Robin Easow Mottackel Marquette University Recommended Citation Mottackel, Robin Easow, "Correlation of Diffusion Tensor Imaging Indices with Histological Parameters in Rat Cervical Spinal Cord Gray Matter Following Distal Contusion Spinal Cord Injury" (2010). Master's Theses (2009 -). Paper 69. http://epublications.marquette.edu/theses_open/69 CORRELATION OF DIFFUSION TENSOR IMAGING INDICES WITH HISTOLOGICAL PARAMETERS IN RAT CERVICAL SPINAL CORD GRAY MATTER FOLLOWING DISTAL CONTUSION SPINAL CORD INJURY By Robin E. Mottackel, B.E. A Thesis submitted to the Faculty of the Graduate School, Marquette University, in Partial Fulfillment of the Requirements for the Degree of Master of Science Milwaukee, Wisconsin December 2010 ABSTRACT CORRELATION OF DIFFUSION TENSOR IMAGING INDICES WITH HISTOLOGICAL PARAMETERS IN RAT CERVICAL SPINAL CORD GRAY MATTER FOLLOWING DISTAL CONTUSION SPINAL CORD INJURY Robin E. Mottackel, B.E. Marquette University, 2010 The purpose of this study was to delineate the diffusion tensor imaging (DTI) parameters across the cervical spinal cord gray matter (GM) in a distal (T8) rat contusion spinal cord injury (SCI) model. DTI data were obtained from ex vivo rat spinal cords and registered to corresponding histological slices in samples from the acute through chronic stages of SCI including uninjured control, 2 weeks post injury, 15 weeks post injury and 25 weeks post injury groups (n = 5 in all groups). After imaging, samples were dehydrated, blocked in paraffin, sliced axially and stained with eriochrome cyanine R stain and H&E counter-stain.