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In Vivo Imaging of Microglia-Mediated Axonal Pruning and Modulation By
Combined bioRxivsingle preprintmanuscript doi: https://doi.org/10.1101/2020.06.07.087221 file ; this version posted June 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 In vivo imaging of microglia-mediated axonal pruning and modulation 2 by the complement system 3 Tony K.Y. Lim1 and Edward S. Ruthazer1,2,* 4 1. Department of Neurology & Neurosurgery, Montreal Neurological Institute-Hospital, McGill 5 University, Montreal, Quebec, H3A 2B4; Canada 6 2. Lead Contact 7 *Correspondence: [email protected] 8 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.06.07.087221; this version posted June 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 9 Summary 10 Partial phagocytosis – called trogocytosis – of axons by microglia has been documented in ex vivo 11 preparations but has yet to be observed in vivo. Fundamental questions regarding the mechanisms that 12 modulate axon trogocytosis as well as its function in neural circuit development remain unanswered. 13 Here we used 2-photon live imaging of the developing Xenopus laevis retinotectal circuit to observe 14 axon trogocytosis by microglia in vivo. Amphibian regulator of complement activation 3 (aRCA3) was 15 identified as a neuronally expressed, synapse-associated complement inhibitory molecule. 16 Overexpression of aRCA3 enhanced axonal arborization and inhibited trogocytosis, while expression of 17 VAMP2-C3, a complement-enhancing fusion protein tethered to the axon surface, reduced axonal 18 arborization. -
Projections from the Trigeminal Nuclear Complex to the Cochlear Nuclei: a Retrograde and Anterograde Tracing Study in the Guinea Pig
Journal of Neuroscience Research 78:901–907 (2004) Projections From the Trigeminal Nuclear Complex to the Cochlear Nuclei: a Retrograde and Anterograde Tracing Study in the Guinea Pig Jianxun Zhou and Susan Shore* Department of Otolaryngology and Kresge Hearing Research Institute, University of Michigan, Ann Arbor, Michigan In addition to input from auditory centers, the cochlear cuneate nucleus innervation of cochlear nucleus has been nucleus (CN) receives inputs from nonauditory centers, hypothesized to convey information about head and pinna including the trigeminal sensory complex. The detailed position for the purpose of localizing a sound source in anatomy, however, and the functional implications of the space (Young et al., 1995). In addition, interactions be- nonauditory innervation of the auditory system are not tween somatosensory and auditory systems have been fully understood. We demonstrated previously that the linked increasingly to phantom sound perception, also trigeminal ganglion projects to CN, with terminal labeling known as tinnitus. This is demonstrated in the observa- most dense in the marginal cell area and secondarily in tions that injuries of the head and neck region can lead to the magnocellular area of the ventral cochlear nucleus the onset of tinnitus in patients with no hearing loss (VCN). We continue this line of study by investigating the (Lockwood et al., 1998). projection from the spinal trigeminal nucleus to CN in We demonstrated previously projections from the guinea pig. After injections of the retrograde tracers Flu- trigeminal ganglion to CN in guinea pigs (Shore et al., oroGold or biotinylated dextran amine (BDA) in VCN, 2000). Terminal labeling of trigeminal ganglion projec- labeled cells were found in the spinal trigeminal nuclei, tions to the CN was found to be most dense in the most densely in the pars interpolaris and pars caudalis marginal cell area and secondarily in the magnocellular with ipsilateral dominance. -
Microglia Control Glutamatergic Synapses in the Adult Mouse Hippocampus
bioRxiv preprint doi: https://doi.org/10.1101/2021.02.01.429096; this version posted February 2, 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. Microglia control glutamatergic synapses in the adult mouse hippocampus Short title: Microglia and glutamatergic synapses Bernadette Basilico1†*‡, Laura Ferrucci1‡, Patrizia Ratano2‡, Maria T. Golia1, Alfonso Grimaldi3, Maria Rosito3, Valentina Ferretti4, Ingrid Reverte1,5, Maria C. Marrone6, Maria Giubettini3,7, Valeria De Turris3, Debora Salerno3, Stefano Garofalo1, Marie-Kim St-Pierre8, Micael Carrier8, Massimiliano Renzi1, Francesca Pagani3, Marcello Raspa9, Ferdinando Scavizzi9, Cornelius T. Gross10, Silvia Marinelli5, Marie E. Tremblay8,11, Daniele Caprioli1,5, Laura Maggi1, Cristina Limatola1,2, Silvia Di Angelantonio1,3§, Davide Ragozzino1,5*§ 1Department of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy. 2IRCCS Neuromed, Via Atinese 18, 86077, Pozzilli, IS, Italy. 3Center for Life Nanoscience, Istituto Italiano di Tecnologia, Rome, Italy. 4Dipartimento di Biologia e Biotecnologie "Charles Darwin", Sapienza University of Rome, Rome, Italy. 5Santa Lucia Foundation (IRCCS Fondazione Santa Lucia), Rome, Italy. 6European Brain Research Institute-Rita Levi Montalcini, Rome, Italy. 7CrestOptics S.p.A., Via di Torre Rossa 66, 00165 Rome, Italy. 8Centre de Recherche du CHU de Québec, Axe Neurosciences Québec, QC, Canada; Département de médecine moléculaire, Université Laval Québec, QC, Canada. 9National Research Council, Institute of Biochemistry and Cell Biology (CNR- IBBC/EMMA/Infrafrontier/IMPC), International Campus “A. Buzzati-Traverso”, Monterotondo (Rome) Italy. -
Neuroglial Response to Neuron Injury. a Study Using Intraneural Injection of Ricinus Communis Agglutinin-60
J. Anat. (1989), 164, pp. 201-213 201 With 16 figures Printed in Great Britain Neuroglial response to neuron injury. A study using intraneural injection of ricinus communis agglutinin-60 E. A. LING, C. Y. WEN*, J. Y. SHIEH*, T. Y. YICK AND S. K. LEONG Department of Anatomy, Faculty of Medicine, National University of Singapore, Singapore 0511 and * Department of Anatomy, College of Medicine, National Taiwan University, Taipei, Taiwan 10018 (Accepted 27 September 1988) INTRODUCTION Several studies have shown that ricinus communis agglutinin (RCA), when injected into a nerve in minute amounts, is retrogradely transported by axons in the nerve, resulting in a selective destruction of the parental cell bodies. Thus, the administration of RCA into the vagus nerve would cause a selective destruction of the efferent neurons in the dorsal motor nucleus (Wiley, Blessing & Reis, 1982; Ling & Leong, 1987, 1988). Such a 'suicide transport' of the toxic lectin is also evident in sensory neurons (Yamamoto, Iwasaki & Konno, 1983, 1984; Johnson, Westrum, Henry & Canfield, 1985; Wiley & Oeltmann, 1986). Recently, the use of RCA has become increasingly important as a research tool for tracing the central projections of primary afferents of peripheral nerves (Yamamoto et al. 1983; Leong & Tan, 1987; Ling & Leong, 1987). While much is known about the consequent death of neurons following RCA application, little is known about the response of the non-neuronal cells either closely associated with, or in the vicinity of, the degenerating neurons. According to Yamamoto et al. (1984), the selective destruction of neurons in the trigeminal and dorsal root ganglia by RCA could possibly stimulate the capsule cells involved in the phagocytosis of the degenerating nerve cells. -
The Functional Organization of Descending Sensory-Motor 2 Pathways in Drosophila 3 4 5 Shigehiro Namiki,1 Michael H
bioRxiv preprint doi: https://doi.org/10.1101/231696; this version posted December 11, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 The functional organization of descending sensory-motor 2 pathways in Drosophila 3 4 5 Shigehiro Namiki,1 Michael H. Dickinson,2 Allan M. Wong,1 Wyatt Korff,1 Gwyneth M. 6 Card,1,* 7 8 1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA 9 2Division of Biology and Bioengineering, California Institute of Technology, Pasadena, CA 91125, USA 10 11 12 This manuscript includes 55 pages of typescript, 15 figures, 0 tables, 24 supplemental figures, and 6 13 supplementary tables. 14 15 KEYWORDS: command neuron; descending neuron; motor control; neuron database; ventral 16 nervous system 17 18 *Correspondence should be addressed to [email protected] (G.M.C) 19 1 bioRxiv preprint doi: https://doi.org/10.1101/231696; this version posted December 11, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 20 SUMMARY 21 22 In most animals, the brain controls the body via a set of descending neurons (DNs) that traverse the neck 23 and terminate in post-cranial regions of the nervous system. This critical neural population is thought to 24 activate, maintain and modulate locomotion and other behaviors. Although individual members of this 25 cell class have been well-studied across species ranging from insects to primates, little is known about the 26 overall connectivity pattern of DNs as a population. -
Structural and Developmental Principles of Neuropil Assembly in C
Article Structural and developmental principles of neuropil assembly in C. elegans https://doi.org/10.1038/s41586-020-03169-5 Mark W. Moyle1, Kristopher M. Barnes2, Manik Kuchroo3, Alex Gonopolskiy3, Leighton H. Duncan1, Titas Sengupta1, Lin Shao1, Min Guo4, Anthony Santella2, Received: 21 April 2020 Ryan Christensen4, Abhishek Kumar5, Yicong Wu4, Kevin R. Moon6, Guy Wolf7, Accepted: 12 November 2020 Smita Krishnaswamy3,10, Zhirong Bao2,10, Hari Shroff4,5,10, William A. Mohler8,10 & Daniel A. Colón-Ramos1,5,9,10 ✉ Published online: xx xx xxxx Check for updates Neuropil is a fundamental form of tissue organization within the brain1, in which densely packed neurons synaptically interconnect into precise circuit architecture2,3. However, the structural and developmental principles that govern this nanoscale precision remain largely unknown4,5. Here we use an iterative data coarse-graining algorithm termed ‘difusion condensation’6 to identify nested circuit structures within the Caenorhabditis elegans neuropil, which is known as the nerve ring. We show that the nerve ring neuropil is largely organized into four strata that are composed of related behavioural circuits. The stratifed architecture of the neuropil is a geometrical representation of the functional segregation of sensory information and motor outputs, with specifc sensory organs and muscle quadrants mapping onto particular neuropil strata. We identify groups of neurons with unique morphologies that integrate information across strata and that create neural structures that cage the strata within the nerve ring. We use high resolution light-sheet microscopy7,8 coupled with lineage-tracing and cell-tracking algorithms9,10 to resolve the developmental sequence and reveal principles of cell position, migration and outgrowth that guide stratifed neuropil organization. -
The Nuclear Pattern of the Non-Tectal Portions of the Midbrain and Isthmus in Primates
THE NUCLEAR PATTERN OF THE NON-TECTAL PORTIONS OF THE MIDBRAIN AND ISTHMUS IN PRIMATES ELIZABETH C. CROSBY AND RUSSELL T. WOODBURNE Department of Anatomy, University of Michigan FOURTEEN PLATES (TWENTY-THREE FIGURES) INTRODUCTION The various nuclear groups in the midbrain of primates show marked resemblances to their homologues in subprimate forms, although certain regions are characterized by a marked increase and others by a definite decrease in development. The literature dealing with special regions is considerable in amount and some of it is of relatively early date. That pertinent to the present consideration of these regions has been reviewed under the account of the general literature placed at the end of this series of papers. Attention is called here to a few contributions that have been particularly helpful in the preparation of the primate descriptions. Among such are the studies of Ziehen on various regions of the midbrain, particularly his account of the periventricular regions, and the descriptive analysis of Ingram and Ranson ('35) of the nucleus of Darkschewitsch and the interstitial nucleus of the medial longitudinal fasciculus, which confirmed Stengel's ( '24) earlier account. There are innumerable figures and descrip- tions of various parts of the oculomotor and trochlear gray in primates. Among these may be mentioned the work of Panegrossi ('04), Ram6n y Cajal ('ll), Brouwer ('18, and elsewhere), Le Gros Clark ( '26) and Mingazzini ( '28). The differences in nomenclature with respect to the periventricular gray of caudal midbrain and isthmus regions are indicated 441 442 G. CARL HUBER ET AL. to some extent on the figures of the human brain as well as considered in the general literature. -
Oligodendrocyte Precursor Cells Sculpt the Visual System by Regulating Axonal Remodeling
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.11.434829; this version posted March 12, 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. 1 Oligodendrocyte Precursor Cells Sculpt the Visual System by Regulating 2 Axonal Remodeling 3 4 Yan Xiao1, Laura J Hoodless2, Luigi Petrucco3,4, Ruben Portugues2,4,5, Tim Czopka1,2,5 5 1) Institute of Neuronal Cell Biology, Technical University of Munich, Germany 6 2) Centre for Clinical Brain Sciences, University of Edinburgh, United Kingdom 7 3) Max Planck Institute of Neurobiology, Sensorimotor Control Research Group, Martinsried 82152, 8 Germany 9 4) Institute of Neuroscience, Technical University of Munich, Germany 10 5) Munich Cluster for Systems Neurology (SyNergy), Germany 11 12 13 *Correspondence to 14 15 Dr. Tim Czopka 16 University of Edinburgh 17 Centre for Clinical Brain Sciences 18 Chancellor's Building 19 49 Little France Crescent 20 Edinburgh EH16 4SB, United Kingdom 21 [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2021.03.11.434829; this version posted March 12, 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. 22 Abstract 23 Many oligodendrocyte precursor cells (OPCs) do not differentiate to form myelin, suggesting 24 additional roles of this cell population. -
Somatotopic Organization of Perioral Musculature Innervation Within the Pig Facial Motor Nucleus
Original Paper Brain Behav Evol 2005;66:22–34 Received: September 20, 2004 Returned for revision: November 10, 2004 DOI: 10.1159/000085045 Accepted after revision: December 7, 2004 Published online: April 8, 2005 Somatotopic Organization of Perioral Musculature Innervation within the Pig Facial Motor Nucleus Christopher D. Marshall a Ron H. Hsu b Susan W. Herring c aTexas A&M University at Galveston, Galveston, Tex., bDepartment of Pediatric Dentistry, University of North Carolina, Chapel Hill, N.C., and cDepartment of Orthodontics, University of Washington, Seattle, Wash., USA Key Words pools of the lateral 4 of the 7 subnuclei of the facial motor Somatotopy W Innervation W Facial nucleus W Perioral nucleus. The motor neuron pools of the perioral muscles muscles W Orbicularis oris W Buccinator W Mammals were generally segregated from motoneurons innervat- ing other facial muscles of the rostrum. However, motor neuron pools were not confined to single nuclei but Abstract instead spanned across 3–4 subnuclei. Perioral muscle The orbicularis oris and buccinator muscles of mammals motor neuron pools overlapped but were organized so- form an important subset of the facial musculature, the matotopically. Motor neuron pools of portions of the perioral muscles. In many taxa, these muscles form a SOO overlapped greatly with each other but exhibited a robust muscular hydrostat capable of highly manipula- crude somatotopy within the SOO motor neuron pool. tive fine motor movements, likely accompanied by a spe- The large and somatotopically organized SOO motor cialized pattern of innervation. We conducted a retro- neuron pool in pigs suggests that the upper lip might be grade nerve-tracing study of cranial nerve (CN) VII in pigs more richly innervated than the other perioral muscles (Sus scrofa) to: (1) map the motor neuron pool distribu- and functionally divided. -
Monosynaptic Premotor Circuit Tracing Reveals Neural Substrates for Oro-Motor Coordination
1 Title 2 3 Monosynaptic Premotor Circuit Tracing Reveals Neural Substrates 4 for Oro-motor Coordination 5 6 7 8 9 10 11 Authors and affiliations 12 13 Edward Stanek IV1, Steven Cheng1, Jun Takatoh1, Bao-Xia Han1, and Fan Wang1, 2 * 14 15 1. Department of Neurobiology, Duke University Medical Center, Durham, NC 27710. 16 2. Department of Cell Biology, Duke University Medical Center, Durham, NC 27710. 17 18 19 20 21 22 Corresponding author 23 24 *Fan Wang 25 Department of Neurobiology, Box 3209 26 Duke University Medical Center 27 Durham, NC 27710 28 Phone: 919-684-3682 29 e-mail: [email protected] 30 31 Number of pages: 59 32 Number of Figures: 10 33 Number of Movies: 4 34 Number of Tables: 2 35 Number of words, Abstract: 237 36 Number of words, Main Text: 5,168 1 37 ABSTRACT 38 39 Feeding behaviors require intricately coordinated activation among the muscles of the jaw, 40 tongue, and face, but the neural anatomical substrates underlying such coordination remain 41 unclear. Here we investigate whether the premotor circuitry of jaw and tongue motoneurons 42 contain elements for coordination. Using a modified monosynaptic rabies virus based 43 transsynaptic tracing strategy, we systematically mapped premotor neurons for the jaw-closing 44 masseter muscle and the tongue-protruding genioglossus muscle. The maps revealed that the two 45 groups of premotor neurons are distributed in regions implicated in rhythmogenesis, descending 46 motor control, and sensory feedback. Importantly, we discovered several premotor connection 47 configurations that are ideally suited for coordinating bilaterally symmetric jaw movements, and 48 for enabling co-activation of specific jaw, tongue, and facial muscles. -
Characterization of Oligodendrocyte Lineage Precursor Cells in the Mouse Cerebral Cortex: a Confocal Microscopy Approach to Demyelinating Diseases
IJAE Vol. 115, n. 1/2: 95-102, 2010 ITALIAN JOURNAL OF ANATOMY AND EMBRYOLOGY Characterization of oligodendrocyte lineage precursor cells in the mouse cerebral cortex: a confocal microscopy approach to demyelinating diseases Francesco Girolamo*, Maurizio Strippoli, Mariella Errede, Vincenzo Benagiano, Luisa Roncali, Glauco Ambrosi, Daniela Virgintino Dipartimento di Anatomia Umana e di Istologia ‘Rodolfo Amprino’, Facoltà di Medicina e Chirurgia – Policlinico – Università di Bari, Italia. *Corresponding author, Email: [email protected] Presented at a meeting in honour of Prof. G. Orlandini, Florence, February 15, 2010 Summary The identifi cation of stem cells resident in the adult central nervous system has redirected the focus of research into demyelinating diseases, such as multiple sclerosis, mainly affecting the brain white matter. This immunocytochemical and morphometrical study was carried out by confocal microscopy in the adult mouse cerebral cortex, with the aim of analysing, in the brain grey matter, the characteristics of the oligodendrocyte lineage cells, whose capability to remyeli nate is still controversial. The observations demonstrated the presence in all the cortex layers of glial restricted progenitors, reactive to A2B5 marker, oligodendrocyte precursor cells, expressing the NG2 proteoglycan, and preoligodendrocytes and premyelinating oligodendrocytes, reac tive to the specifi c marker O4. NG2 expressing cells constitute the major immature population of the cortex, since not only oligodendrocyte precursor cells and preoligodendrocytes but also a part of the glial restrict progenitors express the NG2 proteoglycan. Together with the popula tion of these immature cells, a larger population of mature oligodendrocytes was revealed by the classical oligodendrocyte and myelin markers, 2’,3’cyclic nucleotide 3’phosphodiesterase, myelin basic protein and myelin oligodendrocyte glycoprotein. -
Lecture (6) Internal Structures of the Brainstem.Pdf
Internal structures of the Brainstem Neuroanatomy block-Anatomy-Lecture 6 Editing file Objectives At the end of the lecture, students should be able to: ● Distinguish the internal structure of the components of the brain stem in different levels and the specific criteria of each level. 1. Medulla oblongata (closed, mid and open medulla) 2. Pons (caudal and rostral). 3. Midbrain ( superior and inferior colliculi). Color guide ● Only in boys slides in Green ● Only in girls slides in Purple ● important in Red ● Notes in Grey Medulla oblongata Caudal (Closed) Medulla Traversed by the central canal Motor decussation (decussation of the pyramids) ● Formed by pyramidal fibers, (75-90%) cross to the opposite side ● They descend in the lateral white column of the spinal cord as the lateral corticospinal tract. ● The uncrossed fibers form the ventral corticospinal tract Trigeminal sensory nucleus. ● it is the larger sensory nucleus. ● The Nucleus Extends Through the whole length of the brainstem and its note :All CN V afferent sensory information enters continuation of the substantia gelatinosa of the spinal cord. the brainstem through the nerve itself located in the pons. Thus, to reach the spinal nucleus (which ● It lies in all levels of M.O, medial to the spinal tract of the trigeminal. spans the entire brain stem length) in the Caudal ● It receives pain and temperature from face, forehead. Medulla those fibers have to "descend" in what's known as the Spinal Tract of the Trigeminal ● Its tract present in all levels of M.O. is formed of descending (how its sensory and descend?see the note) fibers that terminate in the trigeminal nucleus.