Choroidal Neovascular Membranes Express Toll-Like Receptor 3
Background: Recent evidence has suggested a role for toll-like receptor 3 (TLR3) in experimental models of age-related macular degeneration (AMD). To date, however, few data exist about TLR3 in human AMD. The purpose of this study was to investigate the expression of TLR3 in human choroidal neovascu...
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Veröffentlicht in: | Ophthalmic research 2010-01, Vol.44 (4), p.237-241 |
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creator | Maloney, Shawn C. Antecka, Emilia Orellana, Maria E. Fernandes, Bruno F. Odashiro, Alexandre N. Eghtedari, Masoomeh Burnier, Jr, Miguel N. |
description | Background: Recent evidence has suggested a role for toll-like receptor 3 (TLR3) in experimental models of age-related macular degeneration (AMD). To date, however, few data exist about TLR3 in human AMD. The purpose of this study was to investigate the expression of TLR3 in human choroidal neovascular (CNV) membranes. Methods: Immunostaining for TLR3 was performed on sections of CNV membranes from 8 AMD patients and eyes from 4 donors without CNV. Results: All CNV membranes expressed TLR3 in retinal pigment epithelial (RPE) cells. One was classified as having strong intensity, 5 as having moderate intensity and 2 as having weak intensity. All cases had ≧30% of the RPE cells staining for TLR3, ranging from 30 to 90%. No expression of TLR3 was observed in vascular endothelial cells or fibroblasts in any CNV membrane. In the donor eyes, the RPE cells near the ora serrata stained stronger than those at the posterior pole, where no staining was observed in 3 out of 4 cases. Conclusion: TLR3 was found in all CNV membranes and was expressed exclusively in RPE cells. The observed difference in RPE staining for TLR3 in donor eyes and CNV membranes suggests a possible role for this receptor in human neovascular AMD. |
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To date, however, few data exist about TLR3 in human AMD. The purpose of this study was to investigate the expression of TLR3 in human choroidal neovascular (CNV) membranes. Methods: Immunostaining for TLR3 was performed on sections of CNV membranes from 8 AMD patients and eyes from 4 donors without CNV. Results: All CNV membranes expressed TLR3 in retinal pigment epithelial (RPE) cells. One was classified as having strong intensity, 5 as having moderate intensity and 2 as having weak intensity. All cases had ≧30% of the RPE cells staining for TLR3, ranging from 30 to 90%. No expression of TLR3 was observed in vascular endothelial cells or fibroblasts in any CNV membrane. In the donor eyes, the RPE cells near the ora serrata stained stronger than those at the posterior pole, where no staining was observed in 3 out of 4 cases. Conclusion: TLR3 was found in all CNV membranes and was expressed exclusively in RPE cells. The observed difference in RPE staining for TLR3 in donor eyes and CNV membranes suggests a possible role for this receptor in human neovascular AMD.</description><identifier>ISSN: 0030-3747</identifier><identifier>EISSN: 1423-0259</identifier><identifier>DOI: 10.1159/000313989</identifier><identifier>PMID: 20699627</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Aged ; Aged, 80 and over ; Choroidal Neovascularization - metabolism ; Female ; Humans ; Immunoenzyme Techniques ; Macular Degeneration - metabolism ; Male ; Middle Aged ; Original Paper ; Retinal Pigment Epithelium - metabolism ; Tissue Donors ; Toll-Like Receptor 3 - metabolism</subject><ispartof>Ophthalmic research, 2010-01, Vol.44 (4), p.237-241</ispartof><rights>2010 S. Karger AG, Basel</rights><rights>Copyright © 2010 S. Karger AG, Basel.</rights><rights>Copyright (c) 2010 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-61f3d9a77c30f19f109b7a23e7244e0c9291034959d2a40eb66a7f7e64f1746f3</citedby><cites>FETCH-LOGICAL-c332t-61f3d9a77c30f19f109b7a23e7244e0c9291034959d2a40eb66a7f7e64f1746f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2422,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20699627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maloney, Shawn C.</creatorcontrib><creatorcontrib>Antecka, Emilia</creatorcontrib><creatorcontrib>Orellana, Maria E.</creatorcontrib><creatorcontrib>Fernandes, Bruno F.</creatorcontrib><creatorcontrib>Odashiro, Alexandre N.</creatorcontrib><creatorcontrib>Eghtedari, Masoomeh</creatorcontrib><creatorcontrib>Burnier, Jr, Miguel N.</creatorcontrib><title>Choroidal Neovascular Membranes Express Toll-Like Receptor 3</title><title>Ophthalmic research</title><addtitle>Ophthalmic Res</addtitle><description>Background: Recent evidence has suggested a role for toll-like receptor 3 (TLR3) in experimental models of age-related macular degeneration (AMD). To date, however, few data exist about TLR3 in human AMD. The purpose of this study was to investigate the expression of TLR3 in human choroidal neovascular (CNV) membranes. Methods: Immunostaining for TLR3 was performed on sections of CNV membranes from 8 AMD patients and eyes from 4 donors without CNV. Results: All CNV membranes expressed TLR3 in retinal pigment epithelial (RPE) cells. One was classified as having strong intensity, 5 as having moderate intensity and 2 as having weak intensity. All cases had ≧30% of the RPE cells staining for TLR3, ranging from 30 to 90%. No expression of TLR3 was observed in vascular endothelial cells or fibroblasts in any CNV membrane. In the donor eyes, the RPE cells near the ora serrata stained stronger than those at the posterior pole, where no staining was observed in 3 out of 4 cases. Conclusion: TLR3 was found in all CNV membranes and was expressed exclusively in RPE cells. The observed difference in RPE staining for TLR3 in donor eyes and CNV membranes suggests a possible role for this receptor in human neovascular AMD.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Choroidal Neovascularization - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Macular Degeneration - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original Paper</subject><subject>Retinal Pigment Epithelium - metabolism</subject><subject>Tissue Donors</subject><subject>Toll-Like Receptor 3 - metabolism</subject><issn>0030-3747</issn><issn>1423-0259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpd0E1Lw0AQBuBFFFurB-8iwYt4iM5-ZNcFL1LqB1QFqeewSWY1beLG3Ub037vS2oOngeGZYeYl5JDCOaWZvgAATrm-1FtkSAXjKbBMb5NhbEPKlVADshfCHCBiDbtkwEBqLZkakqvxm_OurkyTPKL7NKHsG-OTB2wLb94xJJOvzmMIycw1TTqtF5g8Y4nd0vmE75Mda5qAB-s6Ii83k9n4Lp0-3d6Pr6dpyTlbppJaXmmjVMnBUm0p6EIZxlExIRBKzTQFLnSmK2YEYCGlUVahFJYqIS0fkdPV3s67jx7DMm_rUGLTxAtdH3Il42dMZCzKk39y7nr_Ho-LKAqgjEd0tkKldyF4tHnn69b475xC_htovgk02uP1wr5osdrIvwQjOFqBhfGv6DdgPf8DNFd2HA</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Maloney, Shawn C.</creator><creator>Antecka, Emilia</creator><creator>Orellana, Maria E.</creator><creator>Fernandes, Bruno F.</creator><creator>Odashiro, Alexandre N.</creator><creator>Eghtedari, Masoomeh</creator><creator>Burnier, Jr, Miguel N.</creator><general>S. 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To date, however, few data exist about TLR3 in human AMD. The purpose of this study was to investigate the expression of TLR3 in human choroidal neovascular (CNV) membranes. Methods: Immunostaining for TLR3 was performed on sections of CNV membranes from 8 AMD patients and eyes from 4 donors without CNV. Results: All CNV membranes expressed TLR3 in retinal pigment epithelial (RPE) cells. One was classified as having strong intensity, 5 as having moderate intensity and 2 as having weak intensity. All cases had ≧30% of the RPE cells staining for TLR3, ranging from 30 to 90%. No expression of TLR3 was observed in vascular endothelial cells or fibroblasts in any CNV membrane. In the donor eyes, the RPE cells near the ora serrata stained stronger than those at the posterior pole, where no staining was observed in 3 out of 4 cases. Conclusion: TLR3 was found in all CNV membranes and was expressed exclusively in RPE cells. The observed difference in RPE staining for TLR3 in donor eyes and CNV membranes suggests a possible role for this receptor in human neovascular AMD.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>20699627</pmid><doi>10.1159/000313989</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Choroidal Neovascularization - metabolism Female Humans Immunoenzyme Techniques Macular Degeneration - metabolism Male Middle Aged Original Paper Retinal Pigment Epithelium - metabolism Tissue Donors Toll-Like Receptor 3 - metabolism |
title | Choroidal Neovascular Membranes Express Toll-Like Receptor 3 |
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