Mammalian Retinal Cell Quantification

Normal retina and its cell layers are essential for processing visual stimuli, and loss of its integrity has been documented in many disease processes. The numbers and the axonal processes of retinal ganglion cells are reduced substantially in glaucoma, leading to vision loss and blindness. Similarl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Toxicologic pathology 2021-04, Vol.49 (3), p.505-520
Hauptverfasser: Muthuswamy, Anantharaman, Chen, Henry, Hu, Ying, Turner, Oliver C., Aina, Olulanu H.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 520
container_issue 3
container_start_page 505
container_title Toxicologic pathology
container_volume 49
creator Muthuswamy, Anantharaman
Chen, Henry
Hu, Ying
Turner, Oliver C.
Aina, Olulanu H.
description Normal retina and its cell layers are essential for processing visual stimuli, and loss of its integrity has been documented in many disease processes. The numbers and the axonal processes of retinal ganglion cells are reduced substantially in glaucoma, leading to vision loss and blindness. Similarly, selective loss of photoreceptors in age-related macular degeneration and hereditary retinal dystrophies also results in the compromise of visual acuity. Development of genetically modified mice has led to increased understanding of the pathogenesis of many retinal diseases. Similarly, in this digital era, usage of modalities to quantify the retinal cell loss has grown exponentially leading to a better understanding of the suitability of animal models to study human retinal diseases. These quantification modalities provide valuable quantifiable data in studying pathogenesis and disease progression. This review will discuss the immunohistochemical markers for various retinal cells, available automated tools to quantify retinal cells, and present an example of retinal ganglion cell quantification using HALO image analysis platform. Additionally, we briefly review retinal cell types and subtypes, salient features of retina in various laboratory animal species, and a few of the main disease processes that affect retinal cell numbers in humans.
doi_str_mv 10.1177/0192623320976375
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2474465086</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_0192623320976375</sage_id><sourcerecordid>2474465086</sourcerecordid><originalsourceid>FETCH-LOGICAL-c290t-b9677d1f6ad9cd19c05041feaa7724b5c5be3678d009de7c11ecaefac1ffbb5a3</originalsourceid><addsrcrecordid>eNp1kDtPwzAUhS0EoqWwM6EuSCyBe-PYjkdUlYdUhEAwWzeOjVzlUeJk4N-TqoUBiekO5ztHVx9j5wjXiErdAOpUppynoJXkShywKQrOE5SAh2y6jZNtPmEnMa4BMMcMjtmEc55DqmDKLp-orqkK1MxfXR8aquYLV1Xzl4GaPvhgqQ9tc8qOPFXRne3vjL3fLd8WD8nq-f5xcbtKbKqhTwotlSrRSyq1LVFbEJChd0RKpVkhrCgclyovAXTplEV0lpwni94XhSA-Y1e73U3Xfg4u9qYO0Y7_UOPaIZo0U1kmBeRyRGGH2q6NsXPebLpQU_dlEMxWjvkrZ6xc7NeHonblb-HHxggkOyDShzPrduhGH_H_wW9Jnmso</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2474465086</pqid></control><display><type>article</type><title>Mammalian Retinal Cell Quantification</title><source>Access via SAGE</source><source>Alma/SFX Local Collection</source><creator>Muthuswamy, Anantharaman ; Chen, Henry ; Hu, Ying ; Turner, Oliver C. ; Aina, Olulanu H.</creator><creatorcontrib>Muthuswamy, Anantharaman ; Chen, Henry ; Hu, Ying ; Turner, Oliver C. ; Aina, Olulanu H.</creatorcontrib><description>Normal retina and its cell layers are essential for processing visual stimuli, and loss of its integrity has been documented in many disease processes. The numbers and the axonal processes of retinal ganglion cells are reduced substantially in glaucoma, leading to vision loss and blindness. Similarly, selective loss of photoreceptors in age-related macular degeneration and hereditary retinal dystrophies also results in the compromise of visual acuity. Development of genetically modified mice has led to increased understanding of the pathogenesis of many retinal diseases. Similarly, in this digital era, usage of modalities to quantify the retinal cell loss has grown exponentially leading to a better understanding of the suitability of animal models to study human retinal diseases. These quantification modalities provide valuable quantifiable data in studying pathogenesis and disease progression. This review will discuss the immunohistochemical markers for various retinal cells, available automated tools to quantify retinal cells, and present an example of retinal ganglion cell quantification using HALO image analysis platform. Additionally, we briefly review retinal cell types and subtypes, salient features of retina in various laboratory animal species, and a few of the main disease processes that affect retinal cell numbers in humans.</description><identifier>ISSN: 0192-6233</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1177/0192623320976375</identifier><identifier>PMID: 33380270</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><ispartof>Toxicologic pathology, 2021-04, Vol.49 (3), p.505-520</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c290t-b9677d1f6ad9cd19c05041feaa7724b5c5be3678d009de7c11ecaefac1ffbb5a3</cites><orcidid>0000-0003-2700-6317 ; 0000-0003-0512-1170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0192623320976375$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0192623320976375$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33380270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muthuswamy, Anantharaman</creatorcontrib><creatorcontrib>Chen, Henry</creatorcontrib><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Turner, Oliver C.</creatorcontrib><creatorcontrib>Aina, Olulanu H.</creatorcontrib><title>Mammalian Retinal Cell Quantification</title><title>Toxicologic pathology</title><addtitle>Toxicol Pathol</addtitle><description>Normal retina and its cell layers are essential for processing visual stimuli, and loss of its integrity has been documented in many disease processes. The numbers and the axonal processes of retinal ganglion cells are reduced substantially in glaucoma, leading to vision loss and blindness. Similarly, selective loss of photoreceptors in age-related macular degeneration and hereditary retinal dystrophies also results in the compromise of visual acuity. Development of genetically modified mice has led to increased understanding of the pathogenesis of many retinal diseases. Similarly, in this digital era, usage of modalities to quantify the retinal cell loss has grown exponentially leading to a better understanding of the suitability of animal models to study human retinal diseases. These quantification modalities provide valuable quantifiable data in studying pathogenesis and disease progression. This review will discuss the immunohistochemical markers for various retinal cells, available automated tools to quantify retinal cells, and present an example of retinal ganglion cell quantification using HALO image analysis platform. Additionally, we briefly review retinal cell types and subtypes, salient features of retina in various laboratory animal species, and a few of the main disease processes that affect retinal cell numbers in humans.</description><issn>0192-6233</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kDtPwzAUhS0EoqWwM6EuSCyBe-PYjkdUlYdUhEAwWzeOjVzlUeJk4N-TqoUBiekO5ztHVx9j5wjXiErdAOpUppynoJXkShywKQrOE5SAh2y6jZNtPmEnMa4BMMcMjtmEc55DqmDKLp-orqkK1MxfXR8aquYLV1Xzl4GaPvhgqQ9tc8qOPFXRne3vjL3fLd8WD8nq-f5xcbtKbKqhTwotlSrRSyq1LVFbEJChd0RKpVkhrCgclyovAXTplEV0lpwni94XhSA-Y1e73U3Xfg4u9qYO0Y7_UOPaIZo0U1kmBeRyRGGH2q6NsXPebLpQU_dlEMxWjvkrZ6xc7NeHonblb-HHxggkOyDShzPrduhGH_H_wW9Jnmso</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Muthuswamy, Anantharaman</creator><creator>Chen, Henry</creator><creator>Hu, Ying</creator><creator>Turner, Oliver C.</creator><creator>Aina, Olulanu H.</creator><general>SAGE Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2700-6317</orcidid><orcidid>https://orcid.org/0000-0003-0512-1170</orcidid></search><sort><creationdate>202104</creationdate><title>Mammalian Retinal Cell Quantification</title><author>Muthuswamy, Anantharaman ; Chen, Henry ; Hu, Ying ; Turner, Oliver C. ; Aina, Olulanu H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c290t-b9677d1f6ad9cd19c05041feaa7724b5c5be3678d009de7c11ecaefac1ffbb5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muthuswamy, Anantharaman</creatorcontrib><creatorcontrib>Chen, Henry</creatorcontrib><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Turner, Oliver C.</creatorcontrib><creatorcontrib>Aina, Olulanu H.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muthuswamy, Anantharaman</au><au>Chen, Henry</au><au>Hu, Ying</au><au>Turner, Oliver C.</au><au>Aina, Olulanu H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mammalian Retinal Cell Quantification</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2021-04</date><risdate>2021</risdate><volume>49</volume><issue>3</issue><spage>505</spage><epage>520</epage><pages>505-520</pages><issn>0192-6233</issn><eissn>1533-1601</eissn><abstract>Normal retina and its cell layers are essential for processing visual stimuli, and loss of its integrity has been documented in many disease processes. The numbers and the axonal processes of retinal ganglion cells are reduced substantially in glaucoma, leading to vision loss and blindness. Similarly, selective loss of photoreceptors in age-related macular degeneration and hereditary retinal dystrophies also results in the compromise of visual acuity. Development of genetically modified mice has led to increased understanding of the pathogenesis of many retinal diseases. Similarly, in this digital era, usage of modalities to quantify the retinal cell loss has grown exponentially leading to a better understanding of the suitability of animal models to study human retinal diseases. These quantification modalities provide valuable quantifiable data in studying pathogenesis and disease progression. This review will discuss the immunohistochemical markers for various retinal cells, available automated tools to quantify retinal cells, and present an example of retinal ganglion cell quantification using HALO image analysis platform. Additionally, we briefly review retinal cell types and subtypes, salient features of retina in various laboratory animal species, and a few of the main disease processes that affect retinal cell numbers in humans.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>33380270</pmid><doi>10.1177/0192623320976375</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-2700-6317</orcidid><orcidid>https://orcid.org/0000-0003-0512-1170</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0192-6233
ispartof Toxicologic pathology, 2021-04, Vol.49 (3), p.505-520
issn 0192-6233
1533-1601
language eng
recordid cdi_proquest_miscellaneous_2474465086
source Access via SAGE; Alma/SFX Local Collection
title Mammalian Retinal Cell Quantification
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T01%3A48%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mammalian%20Retinal%20Cell%20Quantification&rft.jtitle=Toxicologic%20pathology&rft.au=Muthuswamy,%20Anantharaman&rft.date=2021-04&rft.volume=49&rft.issue=3&rft.spage=505&rft.epage=520&rft.pages=505-520&rft.issn=0192-6233&rft.eissn=1533-1601&rft_id=info:doi/10.1177/0192623320976375&rft_dat=%3Cproquest_cross%3E2474465086%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2474465086&rft_id=info:pmid/33380270&rft_sage_id=10.1177_0192623320976375&rfr_iscdi=true