Immunohistological Study of Monkey Foveal Retina
The fovea centralis, an anatomically concave pit located at the center of the macula, is avascular, hypoxic, and characteristic of stem-cell niches of other tissues. We hypothesized that in the fovea, undifferentiated retinal-stem-cell-like cells may exist, and that neurogenesis may occur. Hence, we...
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description | The fovea centralis, an anatomically concave pit located at the center of the macula, is avascular, hypoxic, and characteristic of stem-cell niches of other tissues. We hypothesized that in the fovea, undifferentiated retinal-stem-cell-like cells may exist, and that neurogenesis may occur. Hence, we performed an immunohistological study using cynomolgus monkey retinas. After preparing frozen tissue sections of the retina including the foveal pit, immunostaining was performed for glial fibrillary acidic protein (GFAP), nestin, vimentin, neuron-specific class III β-tubulin (Tuj-1), arrestin 4, neurofilament, CD117, CD44, Ki67, and cellular retinaldehyde-binding protein (CRALBP), followed by fluorescence and/or confocal microscopy examinations. Immunostaining of the tissue sections enabled clear observation of strongly GFAP-positive cells that corresponded to the inner-half layer of the foveolar Müller cell cone. The surface layer of the foveal slope was partially costained with GFAP and vimentin. Tuj-1-positive cells were observed in the innermost layer of the foveolar retina, which spanned to the surrounding ganglion cell layer. Moreover, colocalization of Tuj-1 and GFAP was observed at the foveal pit. The coexpression of CD117 and CD44 was found in the interphotoreceptor matrix of the fovea. The foveolar cone stained positive for both nestin and arrestin 4, however, the photoreceptor layer outside of the foveola displayed weak staining for nestin. Colocalization of nestin and vimentin was observed in the inner half of the Henle layer, while colocalization of nestin and neurofilament was observed in the outer half, predominantly. Scattered Ki67-positive cells were observed in the cellular processes of the outer plexiform layer and the ganglion cell layer around the foveola. Immunostaining for CRALBP was negative in most parts of the GFAP-positive area. The Müller cell cone was divided into GFAP-strongly positive cells, presumably astrocytes, in the inner layer and nestin-positive/GFAP-weakly positive radial glia-like cells in the outer layer. These findings indicated that groups of such undifferentiated cells in the foveola might be involved in maintaining morphology and regeneration. |
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We hypothesized that in the fovea, undifferentiated retinal-stem-cell-like cells may exist, and that neurogenesis may occur. Hence, we performed an immunohistological study using cynomolgus monkey retinas. After preparing frozen tissue sections of the retina including the foveal pit, immunostaining was performed for glial fibrillary acidic protein (GFAP), nestin, vimentin, neuron-specific class III β-tubulin (Tuj-1), arrestin 4, neurofilament, CD117, CD44, Ki67, and cellular retinaldehyde-binding protein (CRALBP), followed by fluorescence and/or confocal microscopy examinations. Immunostaining of the tissue sections enabled clear observation of strongly GFAP-positive cells that corresponded to the inner-half layer of the foveolar Müller cell cone. The surface layer of the foveal slope was partially costained with GFAP and vimentin. Tuj-1-positive cells were observed in the innermost layer of the foveolar retina, which spanned to the surrounding ganglion cell layer. Moreover, colocalization of Tuj-1 and GFAP was observed at the foveal pit. The coexpression of CD117 and CD44 was found in the interphotoreceptor matrix of the fovea. The foveolar cone stained positive for both nestin and arrestin 4, however, the photoreceptor layer outside of the foveola displayed weak staining for nestin. Colocalization of nestin and vimentin was observed in the inner half of the Henle layer, while colocalization of nestin and neurofilament was observed in the outer half, predominantly. Scattered Ki67-positive cells were observed in the cellular processes of the outer plexiform layer and the ganglion cell layer around the foveola. Immunostaining for CRALBP was negative in most parts of the GFAP-positive area. The Müller cell cone was divided into GFAP-strongly positive cells, presumably astrocytes, in the inner layer and nestin-positive/GFAP-weakly positive radial glia-like cells in the outer layer. These findings indicated that groups of such undifferentiated cells in the foveola might be involved in maintaining morphology and regeneration.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-41793-y</identifier><identifier>PMID: 30918305</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 13/51 ; 14/19 ; 14/28 ; 631/532/2182 ; 692/308/2171 ; Animals ; Arrestin ; Arrestins - metabolism ; Astrocytes ; Carrier Proteins - metabolism ; CD44 antigen ; Confocal microscopy ; Eye ; Female ; Fovea Centralis - metabolism ; Glial fibrillary acidic protein ; Glial Fibrillary Acidic Protein - metabolism ; Humanities and Social Sciences ; Hyaluronan Receptors - metabolism ; Hypoxia ; Immunohistochemistry ; Ki-67 Antigen - metabolism ; Macaca fascicularis ; Male ; multidisciplinary ; Nestin ; Nestin - metabolism ; Neurogenesis ; Neuronal-glial interactions ; Proto-Oncogene Proteins c-kit - metabolism ; Radial glial cells ; Regeneration ; Retina ; Retina - metabolism ; Retinaldehyde ; Retinaldehyde-binding protein ; Science ; Science (multidisciplinary) ; Stem cells ; Tubulin ; Vimentin</subject><ispartof>Scientific reports, 2019-03, Vol.9 (1), p.5258-5258, Article 5258</ispartof><rights>The Author(s) 2019</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-84a0ca89b204794e6083b65fe3235d03001d808b4f1e9ab9cd00e04e097ab0de3</citedby><cites>FETCH-LOGICAL-c577t-84a0ca89b204794e6083b65fe3235d03001d808b4f1e9ab9cd00e04e097ab0de3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437146/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437146/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30918305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Tsunehiko</creatorcontrib><creatorcontrib>Nakamura, Kimitoshi</creatorcontrib><creatorcontrib>Oku, Hidehiro</creatorcontrib><creatorcontrib>Horie, Taeko</creatorcontrib><creatorcontrib>Kida, Teruyo</creatorcontrib><creatorcontrib>Takai, Shinji</creatorcontrib><title>Immunohistological Study of Monkey Foveal Retina</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The fovea centralis, an anatomically concave pit located at the center of the macula, is avascular, hypoxic, and characteristic of stem-cell niches of other tissues. We hypothesized that in the fovea, undifferentiated retinal-stem-cell-like cells may exist, and that neurogenesis may occur. Hence, we performed an immunohistological study using cynomolgus monkey retinas. After preparing frozen tissue sections of the retina including the foveal pit, immunostaining was performed for glial fibrillary acidic protein (GFAP), nestin, vimentin, neuron-specific class III β-tubulin (Tuj-1), arrestin 4, neurofilament, CD117, CD44, Ki67, and cellular retinaldehyde-binding protein (CRALBP), followed by fluorescence and/or confocal microscopy examinations. Immunostaining of the tissue sections enabled clear observation of strongly GFAP-positive cells that corresponded to the inner-half layer of the foveolar Müller cell cone. The surface layer of the foveal slope was partially costained with GFAP and vimentin. Tuj-1-positive cells were observed in the innermost layer of the foveolar retina, which spanned to the surrounding ganglion cell layer. Moreover, colocalization of Tuj-1 and GFAP was observed at the foveal pit. The coexpression of CD117 and CD44 was found in the interphotoreceptor matrix of the fovea. The foveolar cone stained positive for both nestin and arrestin 4, however, the photoreceptor layer outside of the foveola displayed weak staining for nestin. Colocalization of nestin and vimentin was observed in the inner half of the Henle layer, while colocalization of nestin and neurofilament was observed in the outer half, predominantly. Scattered Ki67-positive cells were observed in the cellular processes of the outer plexiform layer and the ganglion cell layer around the foveola. Immunostaining for CRALBP was negative in most parts of the GFAP-positive area. The Müller cell cone was divided into GFAP-strongly positive cells, presumably astrocytes, in the inner layer and nestin-positive/GFAP-weakly positive radial glia-like cells in the outer layer. These findings indicated that groups of such undifferentiated cells in the foveola might be involved in maintaining morphology and regeneration.</description><subject>13/100</subject><subject>13/51</subject><subject>14/19</subject><subject>14/28</subject><subject>631/532/2182</subject><subject>692/308/2171</subject><subject>Animals</subject><subject>Arrestin</subject><subject>Arrestins - metabolism</subject><subject>Astrocytes</subject><subject>Carrier Proteins - metabolism</subject><subject>CD44 antigen</subject><subject>Confocal microscopy</subject><subject>Eye</subject><subject>Female</subject><subject>Fovea Centralis - metabolism</subject><subject>Glial fibrillary acidic protein</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Hypoxia</subject><subject>Immunohistochemistry</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Macaca fascicularis</subject><subject>Male</subject><subject>multidisciplinary</subject><subject>Nestin</subject><subject>Nestin - metabolism</subject><subject>Neurogenesis</subject><subject>Neuronal-glial interactions</subject><subject>Proto-Oncogene Proteins c-kit - metabolism</subject><subject>Radial glial cells</subject><subject>Regeneration</subject><subject>Retina</subject><subject>Retina - metabolism</subject><subject>Retinaldehyde</subject><subject>Retinaldehyde-binding protein</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Stem cells</subject><subject>Tubulin</subject><subject>Vimentin</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kctOwzAQRS0EohXwAyxQJTZsAuNHGnuDhBAFJBASj7XlJJM2JYlLnFTK3-OSUgoLvLHlOXPncQk5pnBOgcsLJ2ioZABUBYJGigfdDhkyEGHAOGO7W-8BOXJuDv6ETAmq9smAg6KSQzgkcF-WbWVnuWtsYad5YorRS9Om3chmo0dbvWM3mtgl-u9nbPLKHJK9zBQOj9b3AXmb3Lxe3wUPT7f311cPQRJGURNIYSAxUsW-jUgJHIPk8TjMkDMepsABaCpBxiKjqEyskhQAQSCoyMSQIj8gl73uoo1LTBOsmtoUelHnpak7bU2uf0eqfKandqnHgkdUjL3A2Vqgth8tukaXuUuwKEyFtnWaUeWXEEklPHr6B53btq78eCtKhn5vbEWxnkpq61yN2aYZCnrlie490d4T_eWJ7nzSyfYYm5RvBzzAe8D5UDXF-qf2P7KfBB-W_w</recordid><startdate>20190327</startdate><enddate>20190327</enddate><creator>Ikeda, Tsunehiko</creator><creator>Nakamura, Kimitoshi</creator><creator>Oku, Hidehiro</creator><creator>Horie, Taeko</creator><creator>Kida, Teruyo</creator><creator>Takai, Shinji</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190327</creationdate><title>Immunohistological Study of Monkey Foveal Retina</title><author>Ikeda, Tsunehiko ; Nakamura, Kimitoshi ; Oku, Hidehiro ; Horie, Taeko ; Kida, Teruyo ; Takai, Shinji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-84a0ca89b204794e6083b65fe3235d03001d808b4f1e9ab9cd00e04e097ab0de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>13/100</topic><topic>13/51</topic><topic>14/19</topic><topic>14/28</topic><topic>631/532/2182</topic><topic>692/308/2171</topic><topic>Animals</topic><topic>Arrestin</topic><topic>Arrestins - metabolism</topic><topic>Astrocytes</topic><topic>Carrier Proteins - metabolism</topic><topic>CD44 antigen</topic><topic>Confocal microscopy</topic><topic>Eye</topic><topic>Female</topic><topic>Fovea Centralis - metabolism</topic><topic>Glial fibrillary acidic protein</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Hypoxia</topic><topic>Immunohistochemistry</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Macaca fascicularis</topic><topic>Male</topic><topic>multidisciplinary</topic><topic>Nestin</topic><topic>Nestin - metabolism</topic><topic>Neurogenesis</topic><topic>Neuronal-glial interactions</topic><topic>Proto-Oncogene Proteins c-kit - metabolism</topic><topic>Radial glial cells</topic><topic>Regeneration</topic><topic>Retina</topic><topic>Retina - metabolism</topic><topic>Retinaldehyde</topic><topic>Retinaldehyde-binding protein</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Stem cells</topic><topic>Tubulin</topic><topic>Vimentin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikeda, Tsunehiko</creatorcontrib><creatorcontrib>Nakamura, Kimitoshi</creatorcontrib><creatorcontrib>Oku, Hidehiro</creatorcontrib><creatorcontrib>Horie, Taeko</creatorcontrib><creatorcontrib>Kida, Teruyo</creatorcontrib><creatorcontrib>Takai, Shinji</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Tsunehiko</au><au>Nakamura, Kimitoshi</au><au>Oku, Hidehiro</au><au>Horie, Taeko</au><au>Kida, Teruyo</au><au>Takai, Shinji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistological Study of Monkey Foveal Retina</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-03-27</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>5258</spage><epage>5258</epage><pages>5258-5258</pages><artnum>5258</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The fovea centralis, an anatomically concave pit located at the center of the macula, is avascular, hypoxic, and characteristic of stem-cell niches of other tissues. We hypothesized that in the fovea, undifferentiated retinal-stem-cell-like cells may exist, and that neurogenesis may occur. Hence, we performed an immunohistological study using cynomolgus monkey retinas. After preparing frozen tissue sections of the retina including the foveal pit, immunostaining was performed for glial fibrillary acidic protein (GFAP), nestin, vimentin, neuron-specific class III β-tubulin (Tuj-1), arrestin 4, neurofilament, CD117, CD44, Ki67, and cellular retinaldehyde-binding protein (CRALBP), followed by fluorescence and/or confocal microscopy examinations. Immunostaining of the tissue sections enabled clear observation of strongly GFAP-positive cells that corresponded to the inner-half layer of the foveolar Müller cell cone. The surface layer of the foveal slope was partially costained with GFAP and vimentin. Tuj-1-positive cells were observed in the innermost layer of the foveolar retina, which spanned to the surrounding ganglion cell layer. Moreover, colocalization of Tuj-1 and GFAP was observed at the foveal pit. The coexpression of CD117 and CD44 was found in the interphotoreceptor matrix of the fovea. The foveolar cone stained positive for both nestin and arrestin 4, however, the photoreceptor layer outside of the foveola displayed weak staining for nestin. Colocalization of nestin and vimentin was observed in the inner half of the Henle layer, while colocalization of nestin and neurofilament was observed in the outer half, predominantly. Scattered Ki67-positive cells were observed in the cellular processes of the outer plexiform layer and the ganglion cell layer around the foveola. Immunostaining for CRALBP was negative in most parts of the GFAP-positive area. The Müller cell cone was divided into GFAP-strongly positive cells, presumably astrocytes, in the inner layer and nestin-positive/GFAP-weakly positive radial glia-like cells in the outer layer. These findings indicated that groups of such undifferentiated cells in the foveola might be involved in maintaining morphology and regeneration.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30918305</pmid><doi>10.1038/s41598-019-41793-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/100 13/51 14/19 14/28 631/532/2182 692/308/2171 Animals Arrestin Arrestins - metabolism Astrocytes Carrier Proteins - metabolism CD44 antigen Confocal microscopy Eye Female Fovea Centralis - metabolism Glial fibrillary acidic protein Glial Fibrillary Acidic Protein - metabolism Humanities and Social Sciences Hyaluronan Receptors - metabolism Hypoxia Immunohistochemistry Ki-67 Antigen - metabolism Macaca fascicularis Male multidisciplinary Nestin Nestin - metabolism Neurogenesis Neuronal-glial interactions Proto-Oncogene Proteins c-kit - metabolism Radial glial cells Regeneration Retina Retina - metabolism Retinaldehyde Retinaldehyde-binding protein Science Science (multidisciplinary) Stem cells Tubulin Vimentin |
title | Immunohistological Study of Monkey Foveal Retina |
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