Hyalocytes in idiopathic epiretinal membranes: a correlative light and electron microscopic study
Purpose To describe characteristics of epiretinal cells at the vitreoretinal interface by correlative light and electron microscopy (CLEM). Methods Epiretinal membrane (ERM) specimens and internal limiting membrane (ILM) specimens were harvested by sequential peeling during vitrectomy from 27 eyes w...
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Veröffentlicht in: | Graefe's archive for clinical and experimental ophthalmology 2014-12, Vol.252 (12), p.1887-1894 |
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creator | Schumann, Ricarda G. Gandorfer, Arnd Ziada, Jean Scheler, Renate Schaumberger, Markus M. Wolf, Armin Kampik, Anselm Haritoglou, Christos |
description | Purpose
To describe characteristics of epiretinal cells at the vitreoretinal interface by correlative light and electron microscopy (CLEM).
Methods
Epiretinal membrane (ERM) specimens and internal limiting membrane (ILM) specimens were harvested by sequential peeling during vitrectomy from 27 eyes with idiopathic epiretinal gliosis, and processed for CLEM. Intraoperatively, the presence of posterior vitreous detachment (PVD) was documented. We used anti-vimentin, anti-α-smooth muscle actin (α-SMA), and anti-CD45 as primary antibodies. A fluorescein-tagged immunonanogold cluster was used as secondary antibody and visualized under the fluorescence and transmission electron microscope.
Results
We demonstrated CD45-positive cells specifically labelled at their plasma membranes with ultrastructural features known for hyalocytes, such as oval nucleus with marginal chromatin, vacuoles, dense granules, and thin cytoplasmic protrusions. CD45-positive cells were mostly located on a thick layer of native vitreous collagen. They were covered by newly formed collagen strands with multilayered proliferation of myofibroblasts. We also demonstrated immunoreactivity for vimentin and alpha-SMA. Cell fragments with positive labelling for α-SMA and vimentin were not only found on the vitreal side of the ILM, but also on the retinal side.
Conclusions
By CLEM, the majority of CD45-positive cells in epiretinal cell proliferation were characterized as hyalocytes. In the context of anomalous PVD and vitreoschisis, ultrastructural features and topographic localization of hyalocytes suggest that these cells play a significant role in ERM formation. CLEM enables a more accurate characterization of epiretinal cell proliferation, and therefore, contributes to a better understanding of the pathogenesis of diseases at the vitreoretinal interface. |
doi_str_mv | 10.1007/s00417-014-2841-x |
format | Article |
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To describe characteristics of epiretinal cells at the vitreoretinal interface by correlative light and electron microscopy (CLEM).
Methods
Epiretinal membrane (ERM) specimens and internal limiting membrane (ILM) specimens were harvested by sequential peeling during vitrectomy from 27 eyes with idiopathic epiretinal gliosis, and processed for CLEM. Intraoperatively, the presence of posterior vitreous detachment (PVD) was documented. We used anti-vimentin, anti-α-smooth muscle actin (α-SMA), and anti-CD45 as primary antibodies. A fluorescein-tagged immunonanogold cluster was used as secondary antibody and visualized under the fluorescence and transmission electron microscope.
Results
We demonstrated CD45-positive cells specifically labelled at their plasma membranes with ultrastructural features known for hyalocytes, such as oval nucleus with marginal chromatin, vacuoles, dense granules, and thin cytoplasmic protrusions. CD45-positive cells were mostly located on a thick layer of native vitreous collagen. They were covered by newly formed collagen strands with multilayered proliferation of myofibroblasts. We also demonstrated immunoreactivity for vimentin and alpha-SMA. Cell fragments with positive labelling for α-SMA and vimentin were not only found on the vitreal side of the ILM, but also on the retinal side.
Conclusions
By CLEM, the majority of CD45-positive cells in epiretinal cell proliferation were characterized as hyalocytes. In the context of anomalous PVD and vitreoschisis, ultrastructural features and topographic localization of hyalocytes suggest that these cells play a significant role in ERM formation. CLEM enables a more accurate characterization of epiretinal cell proliferation, and therefore, contributes to a better understanding of the pathogenesis of diseases at the vitreoretinal interface.</description><identifier>ISSN: 0721-832X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-014-2841-x</identifier><identifier>PMID: 25377434</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Actins - metabolism ; Aged ; Aged, 80 and over ; Basement Membrane - ultrastructure ; Biomarkers - metabolism ; Cell Proliferation ; Epiretinal Membrane - metabolism ; Epiretinal Membrane - pathology ; Female ; Humans ; Immunohistochemistry ; Leukocyte Common Antigens - metabolism ; Male ; Medicine ; Medicine & Public Health ; Microscopy, Electron ; Microscopy, Fluorescence ; Middle Aged ; Ophthalmology ; Retinal Disorders ; Vimentin - metabolism ; Vitrectomy ; Vitreous Body - cytology ; Vitreous Detachment - diagnosis</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2014-12, Vol.252 (12), p.1887-1894</ispartof><rights>Springer-Verlag Berlin Heidelberg 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-edabafc4431b2a4ed3e4115c0d92c86d3aa7623d68399106a8e824594b22b4dc3</citedby><cites>FETCH-LOGICAL-c442t-edabafc4431b2a4ed3e4115c0d92c86d3aa7623d68399106a8e824594b22b4dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00417-014-2841-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00417-014-2841-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25377434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schumann, Ricarda G.</creatorcontrib><creatorcontrib>Gandorfer, Arnd</creatorcontrib><creatorcontrib>Ziada, Jean</creatorcontrib><creatorcontrib>Scheler, Renate</creatorcontrib><creatorcontrib>Schaumberger, Markus M.</creatorcontrib><creatorcontrib>Wolf, Armin</creatorcontrib><creatorcontrib>Kampik, Anselm</creatorcontrib><creatorcontrib>Haritoglou, Christos</creatorcontrib><title>Hyalocytes in idiopathic epiretinal membranes: a correlative light and electron microscopic study</title><title>Graefe's archive for clinical and experimental ophthalmology</title><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><description>Purpose
To describe characteristics of epiretinal cells at the vitreoretinal interface by correlative light and electron microscopy (CLEM).
Methods
Epiretinal membrane (ERM) specimens and internal limiting membrane (ILM) specimens were harvested by sequential peeling during vitrectomy from 27 eyes with idiopathic epiretinal gliosis, and processed for CLEM. Intraoperatively, the presence of posterior vitreous detachment (PVD) was documented. We used anti-vimentin, anti-α-smooth muscle actin (α-SMA), and anti-CD45 as primary antibodies. A fluorescein-tagged immunonanogold cluster was used as secondary antibody and visualized under the fluorescence and transmission electron microscope.
Results
We demonstrated CD45-positive cells specifically labelled at their plasma membranes with ultrastructural features known for hyalocytes, such as oval nucleus with marginal chromatin, vacuoles, dense granules, and thin cytoplasmic protrusions. CD45-positive cells were mostly located on a thick layer of native vitreous collagen. They were covered by newly formed collagen strands with multilayered proliferation of myofibroblasts. We also demonstrated immunoreactivity for vimentin and alpha-SMA. Cell fragments with positive labelling for α-SMA and vimentin were not only found on the vitreal side of the ILM, but also on the retinal side.
Conclusions
By CLEM, the majority of CD45-positive cells in epiretinal cell proliferation were characterized as hyalocytes. In the context of anomalous PVD and vitreoschisis, ultrastructural features and topographic localization of hyalocytes suggest that these cells play a significant role in ERM formation. CLEM enables a more accurate characterization of epiretinal cell proliferation, and therefore, contributes to a better understanding of the pathogenesis of diseases at the vitreoretinal interface.</description><subject>Actins - metabolism</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Basement Membrane - ultrastructure</subject><subject>Biomarkers - metabolism</subject><subject>Cell Proliferation</subject><subject>Epiretinal Membrane - metabolism</subject><subject>Epiretinal Membrane - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Leukocyte Common Antigens - metabolism</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Fluorescence</subject><subject>Middle Aged</subject><subject>Ophthalmology</subject><subject>Retinal Disorders</subject><subject>Vimentin - metabolism</subject><subject>Vitrectomy</subject><subject>Vitreous Body - cytology</subject><subject>Vitreous Detachment - diagnosis</subject><issn>0721-832X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kE1r3DAQhkVoSbZJfkAuQdBLLm71ZUvurSxNUwjkkkBuQpZmdxVsy5Hkkv330eKklEJPGtAz78w8CF1Q8oUSIr8mQgSVFaGiYkrQ6uUIrajgdSUJe_yAVkQyWinOHk_Qp5SeSMF5TY_RCau5lIKLFTI3e9MHu8-QsB-xdz5MJu-8xTD5CNmPpscDDF00I6Rv2GAbYoTeZP8bcO-3u4zN6DD0YHMMIx68jSHZMJWIlGe3P0MfN6ZPcP72nqKH6x_365vq9u7nr_X328oKwXIFznRmU2pOO2YEOA6C0toS1zKrGseNkQ3jrlG8bSlpjALFRN2KjrFOOMtP0dWSO8XwPEPKevDJQt-XxcOcNG2YUlK1nBf08z_oU5hjuXShqBQNYYWiC3U4KEXY6Cn6wcS9pkQf_OvFvy7-9cG_fik9l2_JczeA-9PxLrwAbAFS-Rq3EP8a_d_UVw7akdQ</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Schumann, Ricarda G.</creator><creator>Gandorfer, Arnd</creator><creator>Ziada, Jean</creator><creator>Scheler, Renate</creator><creator>Schaumberger, Markus M.</creator><creator>Wolf, Armin</creator><creator>Kampik, Anselm</creator><creator>Haritoglou, Christos</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Hyalocytes in idiopathic epiretinal membranes: a correlative light and electron microscopic study</title><author>Schumann, Ricarda G. ; Gandorfer, Arnd ; Ziada, Jean ; Scheler, Renate ; Schaumberger, Markus M. ; Wolf, Armin ; Kampik, Anselm ; Haritoglou, Christos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-edabafc4431b2a4ed3e4115c0d92c86d3aa7623d68399106a8e824594b22b4dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Actins - metabolism</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Basement Membrane - ultrastructure</topic><topic>Biomarkers - metabolism</topic><topic>Cell Proliferation</topic><topic>Epiretinal Membrane - metabolism</topic><topic>Epiretinal Membrane - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Leukocyte Common Antigens - metabolism</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Fluorescence</topic><topic>Middle Aged</topic><topic>Ophthalmology</topic><topic>Retinal Disorders</topic><topic>Vimentin - metabolism</topic><topic>Vitrectomy</topic><topic>Vitreous Body - cytology</topic><topic>Vitreous Detachment - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schumann, Ricarda G.</creatorcontrib><creatorcontrib>Gandorfer, Arnd</creatorcontrib><creatorcontrib>Ziada, Jean</creatorcontrib><creatorcontrib>Scheler, Renate</creatorcontrib><creatorcontrib>Schaumberger, Markus M.</creatorcontrib><creatorcontrib>Wolf, Armin</creatorcontrib><creatorcontrib>Kampik, Anselm</creatorcontrib><creatorcontrib>Haritoglou, Christos</creatorcontrib><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>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma 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 Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schumann, Ricarda G.</au><au>Gandorfer, Arnd</au><au>Ziada, Jean</au><au>Scheler, Renate</au><au>Schaumberger, Markus M.</au><au>Wolf, Armin</au><au>Kampik, Anselm</au><au>Haritoglou, Christos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hyalocytes in idiopathic epiretinal membranes: a correlative light and electron microscopic study</atitle><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle><stitle>Graefes Arch Clin Exp Ophthalmol</stitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>252</volume><issue>12</issue><spage>1887</spage><epage>1894</epage><pages>1887-1894</pages><issn>0721-832X</issn><eissn>1435-702X</eissn><abstract>Purpose
To describe characteristics of epiretinal cells at the vitreoretinal interface by correlative light and electron microscopy (CLEM).
Methods
Epiretinal membrane (ERM) specimens and internal limiting membrane (ILM) specimens were harvested by sequential peeling during vitrectomy from 27 eyes with idiopathic epiretinal gliosis, and processed for CLEM. Intraoperatively, the presence of posterior vitreous detachment (PVD) was documented. We used anti-vimentin, anti-α-smooth muscle actin (α-SMA), and anti-CD45 as primary antibodies. A fluorescein-tagged immunonanogold cluster was used as secondary antibody and visualized under the fluorescence and transmission electron microscope.
Results
We demonstrated CD45-positive cells specifically labelled at their plasma membranes with ultrastructural features known for hyalocytes, such as oval nucleus with marginal chromatin, vacuoles, dense granules, and thin cytoplasmic protrusions. CD45-positive cells were mostly located on a thick layer of native vitreous collagen. They were covered by newly formed collagen strands with multilayered proliferation of myofibroblasts. We also demonstrated immunoreactivity for vimentin and alpha-SMA. Cell fragments with positive labelling for α-SMA and vimentin were not only found on the vitreal side of the ILM, but also on the retinal side.
Conclusions
By CLEM, the majority of CD45-positive cells in epiretinal cell proliferation were characterized as hyalocytes. In the context of anomalous PVD and vitreoschisis, ultrastructural features and topographic localization of hyalocytes suggest that these cells play a significant role in ERM formation. CLEM enables a more accurate characterization of epiretinal cell proliferation, and therefore, contributes to a better understanding of the pathogenesis of diseases at the vitreoretinal interface.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25377434</pmid><doi>10.1007/s00417-014-2841-x</doi><tpages>8</tpages></addata></record> |
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subjects | Actins - metabolism Aged Aged, 80 and over Basement Membrane - ultrastructure Biomarkers - metabolism Cell Proliferation Epiretinal Membrane - metabolism Epiretinal Membrane - pathology Female Humans Immunohistochemistry Leukocyte Common Antigens - metabolism Male Medicine Medicine & Public Health Microscopy, Electron Microscopy, Fluorescence Middle Aged Ophthalmology Retinal Disorders Vimentin - metabolism Vitrectomy Vitreous Body - cytology Vitreous Detachment - diagnosis |
title | Hyalocytes in idiopathic epiretinal membranes: a correlative light and electron microscopic study |
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