Cargando…
Intrinsisch photosensitive retinale Ganglienzellen
BACKGROUND: Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGC) area third class of photoreceptors in the retina in addition to rods and cones. They are a small heterogeneous population of cells primarily mediating non-image-forming visual functions. OBJECTIVE: This art...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Medizin
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005408/ https://www.ncbi.nlm.nih.gov/pubmed/34350494 http://dx.doi.org/10.1007/s00347-021-01476-4 |
_version_ | 1784686453607890944 |
---|---|
author | Kinder, Leonie Palumaa, Teele Lindner, Moritz |
author_facet | Kinder, Leonie Palumaa, Teele Lindner, Moritz |
author_sort | Kinder, Leonie |
collection | PubMed |
description | BACKGROUND: Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGC) area third class of photoreceptors in the retina in addition to rods and cones. They are a small heterogeneous population of cells primarily mediating non-image-forming visual functions. OBJECTIVE: This article provides an overview of the current understanding of the functions and the diversity of ipRGCs. It moreover gives an insight into clinically and translationally relevant aspects and treatment options. MATERIAL AND METHODS: Narrative review article. RESULTS: ipRGCs make up ~1–2% of all retinal ganglion cells and are divided into 6 specialized subtypes. With the photopigment melanopsin they can trigger light responses without rod or cone input and can relay irradiance information to various centers of the brain. Depending on the subtype, ipRGCs mediate non-image-forming tasks, such as the pupillary light reflex or synchronizing the circadian clock, and image-forming tasks, such as contrast optimization. ipRGCs exhibit differential resilience against optic nerve damage, making them an interesting study object for the development of neuroprotective strategies. In addition, melanopsin is an attractive optogenetic tool for vision restoration. CONCLUSION: Knowledge on ipRGC physiology is indispensable for understanding frequent clinical observations. Their functional and morphological features are the subject of active research, which highlights novel translational strategies. |
format | Online Article Text |
id | pubmed-9005408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Medizin |
record_format | MEDLINE/PubMed |
spelling | pubmed-90054082022-04-14 Intrinsisch photosensitive retinale Ganglienzellen Kinder, Leonie Palumaa, Teele Lindner, Moritz Ophthalmologe Übersichten BACKGROUND: Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGC) area third class of photoreceptors in the retina in addition to rods and cones. They are a small heterogeneous population of cells primarily mediating non-image-forming visual functions. OBJECTIVE: This article provides an overview of the current understanding of the functions and the diversity of ipRGCs. It moreover gives an insight into clinically and translationally relevant aspects and treatment options. MATERIAL AND METHODS: Narrative review article. RESULTS: ipRGCs make up ~1–2% of all retinal ganglion cells and are divided into 6 specialized subtypes. With the photopigment melanopsin they can trigger light responses without rod or cone input and can relay irradiance information to various centers of the brain. Depending on the subtype, ipRGCs mediate non-image-forming tasks, such as the pupillary light reflex or synchronizing the circadian clock, and image-forming tasks, such as contrast optimization. ipRGCs exhibit differential resilience against optic nerve damage, making them an interesting study object for the development of neuroprotective strategies. In addition, melanopsin is an attractive optogenetic tool for vision restoration. CONCLUSION: Knowledge on ipRGC physiology is indispensable for understanding frequent clinical observations. Their functional and morphological features are the subject of active research, which highlights novel translational strategies. Springer Medizin 2021-08-04 2022 /pmc/articles/PMC9005408/ /pubmed/34350494 http://dx.doi.org/10.1007/s00347-021-01476-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access Dieser Artikel wird unter der Creative Commons Namensnennung 4.0 International Lizenz veröffentlicht, welche die Nutzung, Vervielfältigung, Bearbeitung, Verbreitung und Wiedergabe in jeglichem Medium und Format erlaubt, sofern Sie den/die ursprünglichen Autor(en) und die Quelle ordnungsgemäß nennen, einen Link zur Creative Commons Lizenz beifügen und angeben, ob Änderungen vorgenommen wurden. Die in diesem Artikel enthaltenen Bilder und sonstiges Drittmaterial unterliegen ebenfalls der genannten Creative Commons Lizenz, sofern sich aus der Abbildungslegende nichts anderes ergibt. Sofern das betreffende Material nicht unter der genannten Creative Commons Lizenz steht und die betreffende Handlung nicht nach gesetzlichen Vorschriften erlaubt ist, ist für die oben aufgeführten Weiterverwendungen des Materials die Einwilligung des jeweiligen Rechteinhabers einzuholen. Weitere Details zur Lizenz entnehmen Sie bitte der Lizenzinformation auf http://creativecommons.org/licenses/by/4.0/deed.de (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Übersichten Kinder, Leonie Palumaa, Teele Lindner, Moritz Intrinsisch photosensitive retinale Ganglienzellen |
title | Intrinsisch photosensitive retinale Ganglienzellen |
title_full | Intrinsisch photosensitive retinale Ganglienzellen |
title_fullStr | Intrinsisch photosensitive retinale Ganglienzellen |
title_full_unstemmed | Intrinsisch photosensitive retinale Ganglienzellen |
title_short | Intrinsisch photosensitive retinale Ganglienzellen |
title_sort | intrinsisch photosensitive retinale ganglienzellen |
topic | Übersichten |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005408/ https://www.ncbi.nlm.nih.gov/pubmed/34350494 http://dx.doi.org/10.1007/s00347-021-01476-4 |
work_keys_str_mv | AT kinderleonie intrinsischphotosensitiveretinaleganglienzellen AT palumaateele intrinsischphotosensitiveretinaleganglienzellen AT lindnermoritz intrinsischphotosensitiveretinaleganglienzellen |