Histology Assignment
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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. -
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 The copyright holder for this preprint (which was not certified by peer review) is the author/funder.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. -
Openoptix NCLE Study Guide V0.2
OpenOptix NCLE Study Guide Ver. 0.2 This document is licensed under the Creative Commons Attribution 3.0 License. 6/15/2009 1 About This Document The OpenOptix NCLE Study Guide, sponsored by Laramy-K Optical has been written and is maintained by volunteer members of the optical community. This document is completely free to use, share, and distribute. For the latest version please, visit www.openoptix.org or www.laramyk.com. The quality, value, and success of this document are dependent upon your participation. If you benefit from this document, we only ask that you consider doing one or both of the following: 1. Make an effort to share this document with others whom you believe may benefit from its content. 2. Make a knowledge contribution to improve the quality of this document. Examples of knowledge contributions include original (non-copyrighted) written chapters, sections, corrections, clarifications, images, photographs, diagrams, or simple suggestions. With your help, this document will only continue to improve over time. The OpenOptix NCLE Study Guide is a product of the OpenOptix initiative. Taking a cue from the MIT OpenCourseWare initiative and similar programs from other educational institutions, OpenOptix is an initiative to encourage, develop, and host free and open optical education to improve optical care worldwide. By providing free and open access to optical education the goals of the OpenOptix initiative are to: • Improve optical care worldwide by providing free and open access to optical training materials, particularly for parts of the world where training materials and trained professionals may be limited. • Provide opportunities for optical professionals of all skill levels to review and improve their knowledge, allowing them to better serve their customers and patients • Provide staff training material for managers and practitioners • Encourage ABO certification and advanced education for opticians in the U.S. -
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 -
Shape of the Posterior Vitreous Chamber in Human Emmetropia and Myopia
City Research Online City, University of London Institutional Repository Citation: Gilmartin, B., Nagra, M. and Logan, N. S. (2013). Shape of the posterior vitreous chamber in human emmetropia and myopia. Investigative Ophthalmology and Visual Science, 54(12), pp. 7240-7251. doi: 10.1167/iovs.13-12920 This is the published version of the paper. This version of the publication may differ from the final published version. Permanent repository link: https://openaccess.city.ac.uk/id/eprint/14183/ Link to published version: http://dx.doi.org/10.1167/iovs.13-12920 Copyright: City Research Online aims to make research outputs of City, University of London available to a wider audience. Copyright and Moral Rights remain with the author(s) and/or copyright holders. URLs from City Research Online may be freely distributed and linked to. Reuse: Copies of full items can be used for personal research or study, educational, or not-for-profit purposes without prior permission or charge. Provided that the authors, title and full bibliographic details are credited, a hyperlink and/or URL is given for the original metadata page and the content is not changed in any way. City Research Online: http://openaccess.city.ac.uk/ [email protected] Visual Psychophysics and Physiological Optics Shape of the Posterior Vitreous Chamber in Human Emmetropia and Myopia Bernard Gilmartin, Manbir Nagra, and Nicola S. Logan School of Life and Health Sciences, Aston University, Birmingham, United Kingdom Correspondence: Bernard Gilmartin, PURPOSE. To compare posterior vitreous chamber shape in myopia to that in emmetropia. School of Life and Health Sciences, Aston University, Birmingham, UK, METHODS. -
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 -
Ophthalmology Ophthalmology 160.01
Introduction to Ophthalmology Ophthalmology 160.01 Fall 2019 Tuesdays 12:10-1 pm Location: Library, Room CL220&223 University of California, San Francisco WELCOME OBJECTIVES This is a 1-unit elective designed to provide 1st and 2nd year medical students with - General understanding of eye anatomy - Knowledge of the basic components of the eye exam - Recognition of various pathological processes that impact vision - Appreciation of the clinical and surgical duties of an ophthalmologist INFORMATION This elective is composed of 11 lunchtime didactic sessions. There is no required reading, but in this packet you will find some background information on topics covered in the lectures. You also have access to Vaughan & Asbury's General Ophthalmology online through the UCSF library. AGENDA 9/10 Introduction to Ophthalmology Neeti Parikh, MD CL220&223 9/17 Oculoplastics Robert Kersten, MD CL220&223 9/24 Ocular Effects of Systemic Processes Gerami Seitzman, MD CL220&223 10/01 Refractive Surgery Stephen McLeod, MD CL220&223 10/08 Comprehensive Ophthalmology Saras Ramanathan, MD CL220&223 10/15 BREAK- AAO 10/22 The Role of the Microbiome in Eye Disease Bryan Winn, MD CL220&223 10/29 Retinal imaging in patients with hereditary retinal degenerations Jacque Duncan, MD CL220&223 11/05 Pediatric Ophthalmology Maanasa Indaram, MD CL220&223 11/12 Understanding Glaucoma from a Retina Circuit Perspective Yvonne Ou, MD CL220&223 11/19 11/26 Break - Thanksgiving 12/03 Retina/Innovation/Research Daniel Schwartz, MD CL220&223 CONTACT Course Director Course Coordinator Dr. Neeti Parikh Shelle Libberton [email protected] [email protected] ATTENDANCE Two absences are permitted. -
Quantification of Retinal Layer Thickness Changes in Acute Macular
BJO Online First, published on May 11, 2016 as 10.1136/bjophthalmol-2016-308367 Clinical science Br J Ophthalmol: first published as 10.1136/bjophthalmol-2016-308367 on 11 May 2016. Downloaded from Quantification of retinal layer thickness changes in acute macular neuroretinopathy Marion R Munk,1,2,3 Marco Beck,1 Simone Kolb,1 Michael Larsen,4 Steffen Hamann,4 Christophe Valmaggia,5 Martin S Zinkernagel1,3,6 1Department of ABSTRACT METHODS Ophthalmology, Inselspital, Purpose To quantitatively evaluate retinal layer Patient selection and setting Bern University Hospital, University of Bern, Switzerland thickness changes in acute macular neuroretinopathy This retrospective study included 11 patients from 2Department of (AMN). three tertiary referring institutions: Department of Ophthalmology, Northwestern Methods AMN areas were identified using near- Ophthalmology, Inselspital, Bern University Hospital, University, Feinberg School of infrared reflectance (NIR) images. Intraretinal layer University of Bern, Switzerland; Hospital St Gallen, Medicine, Chicago, Illinois, segmentation using Heidelberg software was performed. St Gallen, Switzerland and Rigshospitalet—Glostrup, USA 3Bern Photographic Reading The inbuilt ETDRS -grid was moved onto the AMN lesion University of Copenhagen, Copenhagen, Denmark. Center, Inselspital, Bern and the mean retinal layer thicknesses of the central grid The study adhered to the tenets of the Declaration of University Hospital, University were recorded and compared with the corresponding Helsinki and was approved by the local review board. of Bern, Switzerland area of the fellow eye at initial presentation and during Retrospectively, patients diagnosed with AMN 4Department of Ophthalmology, Rigshospitalet—Glostrup, follow-up. were included in this study. Diagnosis was based on University of Copenhagen, Results Eleven patients were included (mean age the following clinical criteria: (1) Characteristic Glostrup, Denmark 26±6 years). -
Paraneoplastic Retinopathy Associated with Metastatic Cutaneous Melanoma of Unknown Primary Site
PARANEOPLASTIC RETINOPATHY ASSOCIATED WITH METASTATIC CUTANEOUS MELANOMA OF UNKNOWN PRIMARY SITE l 2 l I HA AM KIRATLI , CHARLES E. THIRKILL , SEVGUL BILGI(: , BORA ELDEM YY 1 and ARMAN KE(:ECI Ankara, Turkey and Sacramento, California SUMMARY features of a patient with this rare syndrome are Purpose: To describe further the clinical and immuno described here. logical features of cutaneous melanoma-associated retinopathy, which is an infrequent form of paraneo CASE REPORT plastic syndrome. Methods: We studied the salient clinical and immuno A 66-year-old man without any prior systemic or logical aspects of a 66-year-old man with metastatic ocular problems presented with the complaint of cutaneous melanoma to lymph nodes of unknown mild visual loss of recent onset in his left eye. He had primary site who developed melanoma-associated experienced occasional flashing lights but had no retinopathy. difficulty with night vision. A few days earlier an Results: There was gradual loss of vision in the left eye. incisional biopsy had been done from his right Colour vision and night vision were not affected. Visual axillary region, where rapid enlargement of four or fields showed arcuate defects. A full-field electroretino five lymph nodes each measuring 3 X 2 X 2 cm was gram demonstrated attenuation of the b-wave ampli noticed. tude in the left eye. The a-wave was intact. Indirect His best corrected visual acuity was 6/9 in the right immunofluorescence techniques showed that the anti eye and 6/18 in the left eye. There was no afferent body reactions took place mainly in the outer plexiform pupillary defect. -
Retinal Anatomy and Histology
1 Q Retinal Anatomy and Histology What is the difference between the retina and the neurosensory retina? 2 Q/A Retinal Anatomy and Histology What is the difference between the retina and the neurosensory retina? While often used interchangeably (including, on occasion, in this slide-set), these are technically not synonyms. The term neurosensory retina refers to the neural lining on the inside of the eye, whereas the term retina refers to this neural lining along with the retinal pigmentthree epithelium words (RPE). 3 A Retinal Anatomy and Histology What is the difference between the retina and the neurosensory retina? While often used interchangeably (including, on occasion, in this slide-set), these are technically not synonyms. The term neurosensory retina refers to the neural lining on the inside of the eye, whereas the term retina refers to this neural lining along with the retinal pigment epithelium (RPE). 4 Q Retinal Anatomy and Histology What is the difference between the retina and the neurosensory retina? While often used interchangeably (including, on occasion, in this slide-set), these are technically not synonyms. The term neurosensory retina refers to the neural lining on the inside of the eye, whereas the term retina refers to this neural lining along with the retinal pigment epithelium (RPE). The neurosensory retina contains three classes of cells—what are they? There are five types of neural elements—what are they? What are the three types of glial cells? The two vascular cell types? --? ----PRs ----Bipolar cells ----Ganglion cells ----Amacrine cells ----Horizontal cells --? ----Müeller cells ----Astrocytes ----Microglia --? ----Endothelial cells ----Pericytes 5 A Retinal Anatomy and Histology What is the difference between the retina and the neurosensory retina? While often used interchangeably (including, on occasion, in this slide-set), these are technically not synonyms. -
Anatomy and Physiology of the Afferent Visual System
Handbook of Clinical Neurology, Vol. 102 (3rd series) Neuro-ophthalmology C. Kennard and R.J. Leigh, Editors # 2011 Elsevier B.V. All rights reserved Chapter 1 Anatomy and physiology of the afferent visual system SASHANK PRASAD 1* AND STEVEN L. GALETTA 2 1Division of Neuro-ophthalmology, Department of Neurology, Brigham and Womens Hospital, Harvard Medical School, Boston, MA, USA 2Neuro-ophthalmology Division, Department of Neurology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA INTRODUCTION light without distortion (Maurice, 1970). The tear–air interface and cornea contribute more to the focusing Visual processing poses an enormous computational of light than the lens does; unlike the lens, however, the challenge for the brain, which has evolved highly focusing power of the cornea is fixed. The ciliary mus- organized and efficient neural systems to meet these cles dynamically adjust the shape of the lens in order demands. In primates, approximately 55% of the cortex to focus light optimally from varying distances upon is specialized for visual processing (compared to 3% for the retina (accommodation). The total amount of light auditory processing and 11% for somatosensory pro- reaching the retina is controlled by regulation of the cessing) (Felleman and Van Essen, 1991). Over the past pupil aperture. Ultimately, the visual image becomes several decades there has been an explosion in scientific projected upside-down and backwards on to the retina understanding of these complex pathways and net- (Fishman, 1973). works. Detailed knowledge of the anatomy of the visual The majority of the blood supply to structures of the system, in combination with skilled examination, allows eye arrives via the ophthalmic artery, which is the first precise localization of neuropathological processes.