Anatomy of the Globe 09 Hermann D. Schubert Basic and Clinical
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The Organization of the Inner Nuclear Layer of the Rabbit Retina
The Journal of Neuroscience. January 1995. 15(l): 875-888 The Organization of the Inner Nuclear Layer of the Rabbit Retina Enrica Strettoil and Richard H. Masland2 ‘Istituto di Neurofisiologia del C.N.R., Pisa, Italy; 2Program in Neuroscience and Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts The initial goal of this study was to establish an accounting function (reviewed by Kolb et al., 198 1; Masland, 1988; Cohen of the major classes of cells present in the inner nuclear and Sterling, 1990; WHssle and Boycott, 199 1; Masland, 1992). layer (INL) of the rabbit’s retina. Series of 80-100 radial What one does not know is how many more cell types there sections 1 pm thick were cut from retinal blocks dissected are-how many cells have not yet been encountered by current, at intervals along the vertical meridian. They were photo- essentially trial and error, methods. graphed at high magnification in the light microscope. By The missing cells-those invisible to present staining tech- visualizing the initial segments of processes leaving the so- niques-are important. They represent unseen actors in the ret- mata, we could identify each cell as a bipolar, amacrine, ina’s circuitry. The responses of the retinal ganglion cells are horizontal, or Muller cell. The identifications made by light controlled by all of the neurons afferent to them. If there are microscopy were confirmed by electron microscopy of al- unseen elements afferent to the ganglion cell, our understanding ternating ultrathin sections. On average, bipolar cells made of the creation of ganglion cell responses risks major error. -
MR Imaging of the Orbital Apex
J Korean Radiol Soc 2000;4 :26 9-0 6 1 6 MR Imaging of the Orbital Apex: An a to m y and Pat h o l o g y 1 Ho Kyu Lee, M.D., Chang Jin Kim, M.D.2, Hyosook Ahn, M.D.3, Ji Hoon Shin, M.D., Choong Gon Choi, M.D., Dae Chul Suh, M.D. The apex of the orbit is basically formed by the optic canal, the superior orbital fis- su r e , and their contents. Space-occupying lesions in this area can result in clinical d- eficits caused by compression of the optic nerve or extraocular muscles. Even vas c u l a r changes in the cavernous sinus can produce a direct mass effect and affect the orbit ap e x. When pathologic changes in this region is suspected, contrast-enhanced MR imaging with fat saturation is very useful. According to the anatomic regions from which the lesions arise, they can be classi- fied as belonging to one of five groups; lesions of the optic nerve-sheath complex, of the conal and intraconal spaces, of the extraconal space and bony orbit, of the cav- ernous sinus or diffuse. The characteristic MR findings of various orbital lesions will be described in this paper. Index words : Orbit, diseases Orbit, MR The apex of the orbit is a complex region which con- tains many nerves, vessels, soft tissues, and bony struc- Anatomy of the orbital apex tures such as the superior orbital fissure and the optic canal (1-3), and is likely to be involved in various dis- The orbital apex region consists of the optic nerve- eases (3). -
CHQ-GDL-01074 Acute Management of Open Globe Injuries
Acute management of Open Globe Injuries Document ID CHQ-GDL-01074 Version no. 2.0 Approval date 14/05/2020 Executive sponsor Executive Director Medical Services Effective date 14/05/2020 Author/custodian Director Infection Management and Prevention service, Review date 14/05/2022 Immunology and Rheumatology Supersedes 1.0 Applicable to All Children’s Health Queensland (CHQ) staff Authorisation Executive Director Clinical Services (QCH) Purpose This evidence-based guideline provides clinical practice advice for clinicians for the acute management of children with open globe injuries. A paediatric ophthalmology team must be actively involved in the management of all patients presenting with this condition. Scope This guideline applies to all Children’s Health Queensland (CHQ) Staff treating a child presenting for the management of open globe injury. Related documents • CHQ-GDL-01202 CHQ Paediatric Antibiocard: Empirical Antibiotic Guidelines • CHQ-PROC-01035 Antimicrobial Restrictions • CHQ Antimicrobial Restriction list • CHQ-GDL-01023 Tetanus Prophylaxis in Wound Management CHQ-GDL-01074- Acute management of Open Globe Injuries - 1 - Guideline Introduction Ocular trauma is an important cause of eye morbidity and is a leading cause of non-congenital mono-ocular blindness among children.1 A quarter of a million children present each year with serious ocular trauma. The vast majority of these are preventable.2 Open globe injuries are injuries where the cornea and/or sclera are breached and there is a full-thickness wound of the eye wall.3 It can be further delineated into globe rupture from blunt trauma and lacerations from sharp objects. When a large blunt object impacts onto the eye, there is an instant increase in intraocular pressure and the eye wall yields at its weakest point leading to tissue prolapse.4 Open globe lacerations are caused by sharp objects or projectiles and subdivided into either penetrating or perforating injuries. -
In Vivo Sublayer Analysis of Human Retinal Inner Plexiform Layer Obtained by Visible- Light Optical Coherence Tomography
bioRxiv preprint doi: https://doi.org/10.1101/2021.01.08.425925; this version posted January 10, 2021. 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. In Vivo Sublayer Analysis Of Human Retinal Inner Plexiform Layer Obtained By Visible- Light Optical Coherence Tomography Zeinab Ghassabi*1, Roman V. Kuranov*2,3, Mengfei Wu1, Behnam Tayebi1,4, Yuanbo Wang3, Ian Rubinoff2, Xiaorong Liu5, Gadi Wollstein1,6, Joel S. Schuman1,6, Hao F. Zhang2, and Hiroshi Ishikawa1,6 1 Department of Ophthalmology, NYU Langone Health, New York, NY, United States. 2 Department of Biomedical Engineering, Northwestern University, Evanston, IL, United States. 3 Opticent Inc., Evanston, IL, United States. 4 Neuroscience Institute, NYU Langone Health, NY, United States. 5 Department of Biology, University of Virginia, Charlottesville, VA, United States 6 Department of Biomedical Engineering, New York University Tandon School of Engineering, New York, NY, United States Funding: NIH: R01-EY013178, R01EY029121, R01EY026078, R44EY026466 * These authors contributed equally to this work Correspondence author: Dr. Hiroshi Ishikawa, [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2021.01.08.425925; this version posted January 10, 2021. 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. Purpose: Growing evidence suggests, in glaucoma, the dendritic degeneration of subpopulation of the retinal ganglion cells (RGCs) may precede RGCs soma death. Since different RGCs synapse in different IPL sublayers, visualization of the lamellar structure of the IPL could enable both clinical and fundamental advances in glaucoma understanding and management. -
The Ganglion Cell Complex and Glaucoma
28 MARCH 2014 The ganglion cell complex and glaucoma GLAUCOMA IN ALL its manifestations (Carl Zeiss Meditec) looks for loss Graham Lakkis and clinical variants ultimately leads to of ganglion cell birefringence in the destruction of retinal ganglion cells. circumpapillary retinal nerve fibre BScOptom GradCertOcTher FACO layer. Time domain (TD) and spectral Lead Optometrist, University of Different methods are available to domain (SD) OCTs measure the Melbourne Eyecare Glaucoma Clinic detect ganglion cell damage, such as ganglion cell axons around the optic structural losses at the optic nerve nerve head to determine nerve fibre head (for example, increased C/D ratio, layer thickness and the TSNIT curve. neuroretinal rim thinning or notching) These existing clinical instruments or changes in ganglion cell function concentrate on measuring the axons of such as threshold visual field defects. the retinal ganglion cells adjacent to Existing clinical methods are limited and on the optic nerve head. in their ability to detect ganglion cell damage until there is significant loss. However, retinal ganglion cells are Approximately 40 per cent of ganglion large and complex cells extending cells need to be lost before an early from the inner retina all the way to glaucomatous threshold visual field the lateral geniculate nucleus (LGN) in defect is manifested,1 and the typically the midbrain. Ganglion cells begin at slow progression in optic nerve head the inner plexiform layer (IPL) where changes makes structural glaucoma they synapse with the bipolar and detection difficult until significant rim amacrine cells of the middle retina. tissue is lost. Their cell bodies (soma) make up the ganglion cell layer (GCL) of the inner With the advent of scanning laser retina, and the ganglion cell axons that clinical instruments, newer methods emerge are the retinal nerve fibre layer have been developed to enhance earlier (NFL). -
Meet the Choroid N Optometric Management Joe Pizzimenti, OD, FAAO O Scientific Advisory Boards [email protected] N Zeiss N Zeavision N Thrombogenics N Genentech
10/29/19 Financial Disclosures o Honoraria n Review of Optometry Meet The Choroid n Optometric Management Joe Pizzimenti, OD, FAAO o Scientific Advisory Boards [email protected] n Zeiss n Zeavision n Thrombogenics n Genentech Financial Disclosures Goals for This Course o Consulting Fees n Zeiss o Functional anatomy review n Zeavision n Choroid n Maculogix o Choroid examination and evaluation o Proprietary Interests o Case examples n None o Interactive o Stockholder: Zeavision Questions? 1 10/29/19 The Choroid The Choroid: Structure, o Located between the Function, and Evaluation sclera and the RPE n Extends from ora serrata to optic nerve o Pigmented/vascular tissue .75mm thick o Nourishes the RPE n Choroiocapillaris designed to leak o Absorbs light that passes through retina The Choriod RPE Bruch’s Membrane thickness o Loose connective tissue o Basal lamina of RPE o Melanocytes o Anterior collagenous o Choriocapillaris layer Mel. n Fenestrated endothelium o Elastic layer allows diffusion of o Posterior collagenous proteins CC layer n S__________ regulation o Basal lamina of CC BM n High blood flow endothelium n Very little O-2 extracted, o Contamination of so high venous O-2 Bruch’s can result in sclera d________, CNVM Nourishing the Retina Choroid Microstructure o 2 main sources of blood supply to retina: • Choriocapillaris o Choroidal BVs n Supplies outer retinal • Sattler’s layer layers, including PRs o CRA • Haller’s layer n 4 branches nourish inner retina • Supra - choroid n Run radially toward fovea 2 10/29/19 Imaging the Vascular Layers Imaging the Choroid of the Choroid WHAT IS ENHANCED Imaging the Choroid-EDI DEPTH OCT IMAGING? • EDI-OCT • Enhanced-depth imaging (EDI) OCT modifies the standard technique of image acquisition to better reveal the structural details of the choroid. -
The Distribution of Immune Cells in the Uveal Tract of the Normal Eye
THE DISTRIBUTION OF IMMUNE CELLS IN THE UVEAL TRACT OF THE NORMAL EYE PAUL G. McMENAMIN Perth, Western Australia SUMMARY function of these cells in the normal iris, ciliary body Inflammatory and immune-mediated diseases of the and choroid. The role of such cell types in ocular eye are not purely the consequence of infiltrating inflammation, which will be discussed by other inflammatory cells but may be initiated or propagated authors in this issue, is not the major focus of this by immune cells which are resident or trafficking review; however, a few issues will be briefly through the normal eye. The uveal tract in particular considered where appropriate. is the major site of many such cells, including resident tissue macro phages, dendritic cells and mast cells. This MACRO PHAGES review considers the distribution and location of these and other cells in the iris, ciliary body and choroid in Mononuclear phagocytes arise from bone marrow the normal eye. The uveal tract contains rich networks precursors and after a brief journey in the blood as of both resident macrophages and MHe class 11+ monocytes immigrate into tissues to become macro dendritic cells. The latter appear strategically located to phages. In their mature form they are widely act as sentinels for capturing and sampling blood-borne distributed throughout the body. Macrophages are and intraocular antigens. Large numbers of mast cells professional phagocytes and play a pivotal role as are present in the choroid of most species but are effector cells in cell-mediated immunity and inflam virtually absent from the anterior uvea in many mation.1 In addition, due to their active secretion of a laboratory animals; however, the human iris does range of important biologically active molecules such contain mast cells. -
Ciliary Zonule Sclera (Suspensory Choroid Ligament)
ACTIVITIES Complete Diagrams PNS 18 and 19 Complete PNS 23 Worksheet 3 #1 only Complete PNS 24 Practice Quiz THE SPECIAL SENSES Introduction Vision RECEPTORS Structures designed to respond to stimuli Variable complexity GENERAL PROPERTIES OF RECEPTORS Transducers Receptor potential Generator potential GENERAL PROPERTIES OF RECEPTORS Stimulus causing receptor potentials Generator potential in afferent neuron Nerve impulse SENSATION AND PERCEPTION Stimulatory input Conscious level = perception Awareness = sensation GENERAL PROPERTIES OF RECEPTORS Information conveyed by receptors . Modality . Location . Intensity . Duration ADAPTATION Reduction in rate of impulse transmission when stimulus is prolonged CLASSIFICATION OF RECEPTORS Stimulus Modality . Chemoreceptors . Thermoreceptors . Nociceptors . Mechanoreceptors . Photoreceptors CLASSIFICATION OF RECEPTORS Origin of stimuli . Exteroceptors . Interoceptors . Proprioceptors SPECIAL SENSES Vision Hearing Olfaction Gustation VISION INTRODUCTION 70% of all sensory receptors are in the eye Nearly half of the cerebral cortex is involved in processing visual information Optic nerve is one of body’s largest nerve tracts VISION INTRODUCTION The eye is a photoreceptor organ Refraction Conversion (transduction) of light into AP’s Information is interpreted in cerebral cortex Eyebrow Eyelid Eyelashes Site where conjunctiva merges with cornea Palpebral fissure Lateral commissure Eyelid Medial commissure (a) Surface anatomy of the right eye Figure 15.1a Orbicularis oculi muscle -
The Nature of Foveal Representation Projections from the Nasal Part of the Retinae to Reach the Ipsilateral Hemispheres
PERSPECTIVES OPINION hemiretina, project to the ‘wrong’ laminae of the LGN. These results were taken to show that the crossing of the nasal retinal fibres in the optic chiasm is incomplete, allowing some The nature of foveal representation projections from the nasal part of the retinae to reach the ipsilateral hemispheres. Normally, Michal Lavidor and Vincent Walsh however, foveal stimuli received by the nasal retinae are projected to the contralateral visual Abstract | A fundamental question in visual the visual midline. This is what Descartes1 cortex. A later study10 indicated that the perception is whether the representation of suggested in his description of the visual dendritic coverage of the centre of the fovea the fovea is split at the midline between the system — he identified the pineal gland as the by RGCs provides a possible neural basis for two hemispheres, or bilaterally represented organ of integration (FIG. 1).Unfortunately, 2–3° of bilateral representation of the fovea by overlapping projections of the fovea in this intuitive, appealing explanation is in the central visual pathways. There is also each hemisphere. Here we examine not true, and we therefore have to assume evidence that the nasotemporal overlap psychophysical, anatomical, that the two cerebral hemispheres cooperate increases towards the upper and lower regions neuropsychological and brain stimulation or compete over the representation of the of the retina11. experiments that have addressed this human foveal area. Most studies that have labelled RGCs with question, and argue for a shift from the When a person is fixating centrally (looking HRP after unilateral injections into the mon- current default view of bilateral straight ahead), information that is to key optic tract have found a nasotemporal representation to that of a split the right of fixation (in the right visual field) is overlap zone along the vertical meridian12. -
Affections of Uvea Affections of Uvea
AFFECTIONS OF UVEA AFFECTIONS OF UVEA Anatomy and physiology: • Uvea is the vascular coat of the eye lying beneath the sclera. • It consists of the uvea and uveal tract. • It consists of 3 parts: Iris, the anterior portion; Ciliary body, the middle part; Choroid, the third and the posterior most part. • All the parts of uvea are intimately associated. Iris • It is spongy having the connective tissue stroma, muscular fibers and abundance of vessels and nerves. • It is lined anteriorly by endothelium and posteriorly by a pigmented epithelium. • Its color is because of amount of melanin pigment. Mostly it is brown or golden yellow. • Iris has two muscles; the sphincter which encircles the pupil and has parasympathetic innervation; the dilator which extends from near the sphincter and has sympathetic innervation. • Iris regulates the amount of light admitted to the interior through pupil. • The iris separates the anterior chamber from the posterior chamber of the eye. Ciliary Body: • It extends backward from the base of the iris to the anterior part of the choroid. • It has ciliary muscle and the ciliary processes (70 to 80 in number) which are covered by ciliary epithelium. Choroid: • It is located between the sclera and the retina. • It extends from the ciliaris retinae to the opening of the optic nerve. • It is composed mainly of blood vessels and the pigmented tissue., The pupil • It is circular and regular opening formed by the iris and is larger in dogs in comparison to man. • It contracts or dilates depending upon the light source, due the sphincter and dilator muscles of the iris, respectively. -
Radial and Tangential Dispersion Patterns in the Mouse Retina Are Cell
Proc. Natl. Acad. Sci. USA Vol. 92, pp. 2494-2498, March 1995 Neurobiology Radial and tangential dispersion patterns in the mouse retina are cell-class specific (cell migration/cell lineage/retinal development/transgenic mice/X chromosome inactivation) B. E. REESE*, A. R. HARvEyt, AND S.-S. TANt§ *Neuroscience Research Institute and Department of Psychology, University of California, Santa Barbara, CA 93106; tDepartment of Anatomy and Human Biology, University of Western Australia, Nedlands, WA 6009 Australia; and tDepartment of Anatomy and Cell Biology, University of Melbourne, Parkville, Victoria 3052, Australia Communicated by Pasko Rakic, Yale University School ofMedicine, New Haven, CT, December 16, 1994 ABSTRACT The retina is derived from a pseudostratified retinal cells remain clonally segregated, they should appear as germinal zone in which the relative position of a progenitor distinct groups of blue versus white cells. We have used this cell is believed to determine the position ofthe progeny aligned approach to address the issue of whether radially aligned cells in the radial axis. Such a developmental mechanism would in the mature retina reflect such a clonal derivation. ensure that radial arrays of cells which comprise functional units in the mature central nervous system are also clonally MATERIALS AND METHODS related. The present study has tested this hypothesis by using Retinas from adult transgenic mice, derived from founder line X chromosome-inactivation transgenic mosaic mice. We re- H253, which carries a lacZ transgene -
Semaphorin3a/Neuropilin-1 Signaling Acts As a Molecular Switch Regulating Neural Crest Migration During Cornea Development
Developmental Biology 336 (2009) 257–265 Contents lists available at ScienceDirect Developmental Biology journal homepage: www.elsevier.com/developmentalbiology Semaphorin3A/neuropilin-1 signaling acts as a molecular switch regulating neural crest migration during cornea development Peter Y. Lwigale a,⁎, Marianne Bronner-Fraser b a Department of Biochemistry and Cell Biology, MS 140, Rice University, P.O. Box 1892, Houston, TX 77251, USA b Division of Biology, 139-74, California Institute of Technology, Pasadena, CA 91125, USA article info abstract Article history: Cranial neural crest cells migrate into the periocular region and later contribute to various ocular tissues Received for publication 2 April 2009 including the cornea, ciliary body and iris. After reaching the eye, they initially pause before migrating over Revised 11 September 2009 the lens to form the cornea. Interestingly, removal of the lens leads to premature invasion and abnormal Accepted 6 October 2009 differentiation of the cornea. In exploring the molecular mechanisms underlying this effect, we find that Available online 13 October 2009 semaphorin3A (Sema3A) is expressed in the lens placode and epithelium continuously throughout eye development. Interestingly, neuropilin-1 (Npn-1) is expressed by periocular neural crest but down- Keywords: Semaphorin3A regulated, in a manner independent of the lens, by the subpopulation that migrates into the eye and gives Neuropilin-1 rise to the cornea endothelium and stroma. In contrast, Npn-1 expressing neural crest cells remain in the Neural crest periocular region and contribute to the anterior uvea and ocular blood vessels. Introduction of a peptide that Cornea inhibits Sema3A/Npn-1 signaling results in premature entry of neural crest cells over the lens that Lens phenocopies lens ablation.