Chapter 8 Nervous System
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Oligodendrocytes in Development, Myelin Generation and Beyond
cells Review Oligodendrocytes in Development, Myelin Generation and Beyond Sarah Kuhn y, Laura Gritti y, Daniel Crooks and Yvonne Dombrowski * Wellcome-Wolfson Institute for Experimental Medicine, Queen’s University Belfast, Belfast BT9 7BL, UK; [email protected] (S.K.); [email protected] (L.G.); [email protected] (D.C.) * Correspondence: [email protected]; Tel.: +0044-28-9097-6127 These authors contributed equally. y Received: 15 October 2019; Accepted: 7 November 2019; Published: 12 November 2019 Abstract: Oligodendrocytes are the myelinating cells of the central nervous system (CNS) that are generated from oligodendrocyte progenitor cells (OPC). OPC are distributed throughout the CNS and represent a pool of migratory and proliferative adult progenitor cells that can differentiate into oligodendrocytes. The central function of oligodendrocytes is to generate myelin, which is an extended membrane from the cell that wraps tightly around axons. Due to this energy consuming process and the associated high metabolic turnover oligodendrocytes are vulnerable to cytotoxic and excitotoxic factors. Oligodendrocyte pathology is therefore evident in a range of disorders including multiple sclerosis, schizophrenia and Alzheimer’s disease. Deceased oligodendrocytes can be replenished from the adult OPC pool and lost myelin can be regenerated during remyelination, which can prevent axonal degeneration and can restore function. Cell population studies have recently identified novel immunomodulatory functions of oligodendrocytes, the implications of which, e.g., for diseases with primary oligodendrocyte pathology, are not yet clear. Here, we review the journey of oligodendrocytes from the embryonic stage to their role in homeostasis and their fate in disease. We will also discuss the most common models used to study oligodendrocytes and describe newly discovered functions of oligodendrocytes. -
Neuron Morphology Influences Axon Initial Segment Plasticity1,2,3
New Research Neuronal Excitability Neuron Morphology Influences Axon Initial Segment Plasticity1,2,3 Allan T. Gulledge1 and Jaime J. Bravo2 DOI:http://dx.doi.org/10.1523/ENEURO.0085-15.2016 1Department of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire 03756, and 2Thayer School of Engineering at Dartmouth, Hanover, New Hampshire 03755 Visual Abstract In most vertebrate neurons, action potentials are initiated in the axon initial segment (AIS), a specialized region of the axon containing a high density of voltage-gated sodium and potassium channels. It has recently been proposed that neurons use plasticity of AIS length and/or location to regulate their intrinsic excitability. Here we quantify the impact of neuron morphology on AIS plasticity using computational models of simplified and realistic somatodendritic morphologies. In small neurons (e.g., den- tate granule neurons), excitability was highest when the AIS was of intermediate length and located adjacent to the soma. Conversely, neu- rons having larger dendritic trees (e.g., pyramidal neurons) were most excitable when the AIS was longer and/or located away from the soma. For any given somatodendritic morphology, increasing dendritic mem- brane capacitance and/or conductance favored a longer and more distally located AIS. Overall, changes to AIS length, with corresponding changes in total sodium conductance, were far more effective in regulating neuron excitability than were changes in AIS location, while dendritic capacitance had a larger impact on AIS performance than did dendritic conductance. The somatodendritic influence on AIS performance reflects modest soma- to-AIS voltage attenuation combined with neuron size-dependent changes in AIS input resistance, effective membrane time constant, and isolation from somatodendritic capacitance. -
How Does an Axon Grow?
Downloaded from genesdev.cshlp.org on October 2, 2021 - Published by Cold Spring Harbor Laboratory Press REVIEW How does an axon grow? Jeffrey L. Goldberg1 Department of Neurobiology, Stanford University School of Medicine, Stanford, California 94305, USA How do axons grow during development, and why do cisions to advance, retract, pause, or turn (Fig. 1). All of they fail to regrow when injured? In the complicated these are potential regulatory sites that could control a mesh of our nervous system, the axon is the information neuron’s ability to elongate or regenerate its axon. superhighway, carrying all of the data we use to sense our environment and carry out behaviors. To wire up our Production of the building blocks, nervous system properly, neurons must elongate their both membrane and cytoplasmic axons during development to reach their targets. This is no simple task, however. The complex morphology of Rapid axon growth requires rapid manufacture and sup- axons and dendrites puts neurons among the most intri- ply of cytoplasm and membrane. Where are the lipid and cate and beautiful cells in the body. Knowledge of how protein building blocks made? It was known from classic neurons extend axons and dendrites, elongate at a par- experiments that axons cut off from the cell bodies of ticular rate, and stop growing at the proper time is criti- adult sensory neurons continue to elongate in culture cal to understanding the development of our nervous (Shaw and Bray 1977), but evidence for local production system, yet the regulation of these processes is poorly of membrane and cytoplasmic elements went lacking for understood. -
Regulation of Myelin Structure and Conduction Velocity by Perinodal Astrocytes
Correction NEUROSCIENCE Correction for “Regulation of myelin structure and conduc- tion velocity by perinodal astrocytes,” by Dipankar J. Dutta, Dong Ho Woo, Philip R. Lee, Sinisa Pajevic, Olena Bukalo, William C. Huffman, Hiroaki Wake, Peter J. Basser, Shahriar SheikhBahaei, Vanja Lazarevic, Jeffrey C. Smith, and R. Douglas Fields, which was first published October 29, 2018; 10.1073/ pnas.1811013115 (Proc. Natl. Acad. Sci. U.S.A. 115,11832–11837). The authors note that the following statement should be added to the Acknowledgments: “We acknowledge Dr. Hae Ung Lee for preliminary experiments that informed the ultimate experimental approach.” Published under the PNAS license. Published online June 10, 2019. www.pnas.org/cgi/doi/10.1073/pnas.1908361116 12574 | PNAS | June 18, 2019 | vol. 116 | no. 25 www.pnas.org Downloaded by guest on October 2, 2021 Regulation of myelin structure and conduction velocity by perinodal astrocytes Dipankar J. Duttaa,b, Dong Ho Wooa, Philip R. Leea, Sinisa Pajevicc, Olena Bukaloa, William C. Huffmana, Hiroaki Wakea, Peter J. Basserd, Shahriar SheikhBahaeie, Vanja Lazarevicf, Jeffrey C. Smithe, and R. Douglas Fieldsa,1 aSection on Nervous System Development and Plasticity, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892; bThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD 20817; cMathematical and Statistical Computing Laboratory, Office of Intramural Research, Center for Information -
Cortex Brainstem Spinal Cord Thalamus Cerebellum Basal Ganglia
Harvard-MIT Division of Health Sciences and Technology HST.131: Introduction to Neuroscience Course Director: Dr. David Corey Motor Systems I 1 Emad Eskandar, MD Motor Systems I - Muscles & Spinal Cord Introduction Normal motor function requires the coordination of multiple inter-elated areas of the CNS. Understanding the contributions of these areas to generating movements and the disturbances that arise from their pathology are important challenges for the clinician and the scientist. Despite the importance of diseases that cause disorders of movement, the precise function of many of these areas is not completely clear. The main constituents of the motor system are the cortex, basal ganglia, cerebellum, brainstem, and spinal cord. Cortex Basal Ganglia Cerebellum Thalamus Brainstem Spinal Cord In very broad terms, cortical motor areas initiate voluntary movements. The cortex projects to the spinal cord directly, through the corticospinal tract - also known as the pyramidal tract, or indirectly through relay areas in the brain stem. The cortical output is modified by two parallel but separate re entrant side loops. One loop involves the basal ganglia while the other loop involves the cerebellum. The final outputs for the entire system are the alpha motor neurons of the spinal cord, also called the Lower Motor Neurons. Cortex: Planning and initiation of voluntary movements and integration of inputs from other brain areas. Basal Ganglia: Enforcement of desired movements and suppression of undesired movements. Cerebellum: Timing and precision of fine movements, adjusting ongoing movements, motor learning of skilled tasks Brain Stem: Control of balance and posture, coordination of head, neck and eye movements, motor outflow of cranial nerves Spinal Cord: Spontaneous reflexes, rhythmic movements, motor outflow to body. -
NEURAL CONNECTIONS: Some You Use, Some You Lose
NEURAL CONNECTIONS: Some You Use, Some You Lose by JOHN T. BRUER SOURCE: Phi Delta Kappan 81 no4 264-77 D 1999 . The magazine publisher is the copyright holder of this article and it is reproduced with permission. Further reproduction of this article in violation of the copyright is prohibited JOHN T. BRUER is president of the James S. McDonnell Foundation, St. Louis. This article is adapted from his new book, The Myth of the First Three Years (Free Press, 1999), and is reprinted by arrangement with The Free Press, a division of Simon Schuster Inc. ©1999, John T. Bruer . OVER 20 YEARS AGO, neuroscientists discovered that humans and other animals experience a rapid increase in brain connectivity -- an exuberant burst of synapse formation -- early in development. They have studied this process most carefully in the brain's outer layer, or cortex, which is essentially our gray matter. In these studies, neuroscientists have documented that over our life spans the number of synapses per unit area or unit volume of cortical tissue changes, as does the number of synapses per neuron. Neuroscientists refer to the number of synapses per unit of cortical tissue as the brain's synaptic density. Over our lifetimes, our brain's synaptic density changes in an interesting, patterned way. This pattern of synaptic change and what it might mean is the first neurobiological strand of the Myth of the First Three Years. (The second strand of the Myth deals with the notion of critical periods, and the third takes up the matter of enriched, or complex, environments.) Popular discussions of the new brain science trade heavily on what happens to synapses during infancy and childhood. -
Nomina Histologica Veterinaria, First Edition
NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria. -
New Approaches to Analyse Axon- Oligodendrocyte Communication In
Neuroforum 2017; 23(4): A175–A181 Tim Czopka* and Franziska Auer New Approaches to Analyse Axon- Oligodendrocyte Communication in vivo https://doi.org/10.1515/nf-2017-A010 the temporal timing, with which signals are exchanged between neurons. Abstract: A major challenge for understanding our nerv- The regions in which axons exchange information ous system is to elucidate how its constituting cells coordi- between different brain areas are called the ‘white mat- nate each other to form and maintain a functional organ. ter’ (the grey matter being the areas where neuronal cell The interaction between neurons and oligodendrocytes bodies reside). White matter appears white due to the represents a unique cellular entity. Oligodendrocytes mye- presence of myelin, a fatty coating that surrounds most ax- linate axons by tightly ensheathing them. Myelination reg- ons. Myelin is an evolutionary acquisition of vertebrates, ulates speed of signal transduction, thus communication which electrically insulates axons and enables rapid between neurons, and supports long-term axonal health. and energy efficient signal transmission. It is likely that Despite their importance, we still have large gaps in our these properties have in fact enabled the evolution of our understanding of the mechanisms underlying myelinated complex nervous system with its high cell number. In the axon formation, remodelling and repair. Zebrafish repre- central nervous system (CNS), myelin is produced by spe- sent an increasingly popular model organism, particular- cialised glial cells, the Oligodendrocytes. Genetic defects ly due to their suitability for live cell imaging and genetic that perturb formation or maintenance of myelin (e.g. in manipulation. Here, we provide an overview about this Leukodystrophies) lead to severe motoric and cognitive research area, describe how zebrafish have helped under- symptoms. -
11 Introduction to the Nervous System and Nervous Tissue
11 Introduction to the Nervous System and Nervous Tissue ou can’t turn on the television or radio, much less go online, without seeing some- 11.1 Overview of the Nervous thing to remind you of the nervous system. From advertisements for medications System 381 Yto treat depression and other psychiatric conditions to stories about celebrities and 11.2 Nervous Tissue 384 their battles with illegal drugs, information about the nervous system is everywhere in 11.3 Electrophysiology our popular culture. And there is good reason for this—the nervous system controls our of Neurons 393 perception and experience of the world. In addition, it directs voluntary movement, and 11.4 Neuronal Synapses 406 is the seat of our consciousness, personality, and learning and memory. Along with the 11.5 Neurotransmitters 413 endocrine system, the nervous system regulates many aspects of homeostasis, including 11.6 Functional Groups respiratory rate, blood pressure, body temperature, the sleep/wake cycle, and blood pH. of Neurons 417 In this chapter we introduce the multitasking nervous system and its basic functions and divisions. We then examine the structure and physiology of the main tissue of the nervous system: nervous tissue. As you read, notice that many of the same principles you discovered in the muscle tissue chapter (see Chapter 10) apply here as well. MODULE 11.1 Overview of the Nervous System Learning Outcomes 1. Describe the major functions of the nervous system. 2. Describe the structures and basic functions of each organ of the central and peripheral nervous systems. 3. Explain the major differences between the two functional divisions of the peripheral nervous system. -
Cerebral Cortex
Cerebral Cortex • Research on the structure and function of the brain reveals that there are both specialized and diffuse areas of function • Motor and sensory areas are localized in discrete cortical areas called domains • Many higher mental functions such as memory and language appear to have overlapping domains and are more diffusely located • Broadmann areas are areas of localized function Cerebral Cortex - Generalizations • The cerebral cortex has three types of functional areas – Motor areas / control voluntary motor function – Sensory areas / provide conscious awareness of sensation – Association areas / act mainly to integrate diverse information for purposeful action • Each hemisphere is chiefly concerned with the sensory and motor functions of the opposite (contralateral) side of the body Motor Areas • Cortical areas controlling motor functions lie in the posterior part of the frontal lobes • Motor areas include the primary motor cortex, the premotor cortex, Broca’s area, and the front eye field Primary Motor Cortex • The primary motor cortex is located in the precentral gyrus of the frontal lobe of each hemisphere • Large neurons (pyramidal cells) in these gyri allow us to consciously control the precise or skill voluntary movements of our skeletal muscles Pyramidal cells • These long axons, which project to the spinal cord, form the massive Dendrites voluntary motor tracts called the pyramidal, or corticospinal tracts • All other descending motor tracts issue from brain stem nuclei and consists of chains of two, three, or -
Optimal Feedback Control and the Neural Basis of Volitional Motor Control
REVIEWS OPTIMAL FEEDBACK CONTROL AND THE NEURAL BASIS OF VOLITIONAL MOTOR CONTROL Stephen H. Scott Skilled motor behaviour, from the graceful leap of a ballerina to a precise pitch by a baseball player, appears effortless but reflects an intimate interaction between the complex mechanical properties of the body and control by a highly distributed circuit in the CNS. An important challenge for understanding motor function is to connect these three levels of the motor system — motor behaviour, limb mechanics and neural control. Optimal feedback control theory might provide the important link across these levels of the motor system and help to unravel how the primary motor cortex and other regions of the brain plan and control movement. Perhaps the most surprising feature of the motor system The goal of this review is to bring all three levels of is the ease with which humans and other animals can the motor system together, to illustrate how M1 is move. It is only when we observe the clumsy movements linked to limb physics and motor behaviour. The key of a child, or the motor challenges faced by individuals ingredient is the use of optimal feedback control as a with neurological disorders, that we become aware of model of motor control in which sophisticated behav- the inherent difficulties of motor control. iours are created by low-level control signals (BOX 2). The efforts of systems neuroscientists to understand I begin with a brief review of each level of the motor how the brain controls movement include studies system, followed by a more detailed description of how on the physics of the musculoskeletal system, neuro- optimal feedback control predicts many features of physiological studies to explore neural control, and neural processing in M1. -
Nervous System -I
Body Tissues Epithelial Connective Tissues Muscle Nervous Nervous system Controlling & Coordinating System Conducts nerve impulses between body structures and controls body functions Functions • Sensory Internal External • Integration> Analysis> storage>interpret>decide • Motor> Response • Regulates all activity (Voluntary & Involuntary) • Adjust according to changing external and internal environment Nervous System Subdivisions: CNS (Central Nervous System) PNS( Peripheral Nervous System) ANS (Autonomic Nervous system) Nervous tissue - Cell Types Functionally • Neuron (Nerve Cell) -Conduction Variable Shape , Size, Function • Neuroglia - Supportive -- Macroglia -- Microglia • Ependymal Cells • Schwann Cells - In PNS Neuron ( Nerve Cell) Components 1.Cell Body 2.Cell Processes (Neurites) Cell Body - Size vary from 5 µm - 120 µm (Perikaryon) – Plasma membrane Nucleus Cytoplasm Axon Hillock Neuronal Skeleton Cell Processes 1.Dendrites : Short , irregular thickness. Freely Branching, Afferent processes , Contain Nissl Granules 2. Axon – Long , Single, Efferent process of Uniform Diameter, Devoid of Nissl Granules, Ensheathed by Schwann cells, Gives collateral branches Terminal branches called telodendria (axon terminals) Terminate – within CNS - Always with another neuron Outside CNS – Either may end in relation to the effector organ or Synapse with neurons of Peripheral ganglia Types Of Neuron 1.Acc. To no of Processes Bipolar Multipolar Pseudounipolar 2. Acc. To Function Sensory Motor 3. Acc. To Axon Length Golgi type-1(long) Golgi type-II Synapse site of junction of neuron Types Axo- Dendritic Axo – Somatic Axo- Axonal Neuroglia • Astrocytes : Fibrous Protoplasmic Metabolism of neurotransmitters K+ Balance Contribute in brain development Blood brain barrier Link between neurons and blood vessels • Oligodendrocytes: Form a supporting network around neurons Produce myelin sheath around several neurons Neuroglia- contd. • Microglia: Phagocytic cells; Migrate to area of injured nervous tissue.