Photoreceptor repair in response to RPE transplants in RCS rats: Outer segment regeneration
Purpose. We have previously shown that transplants of normal rat neonatal RPE cells rescued photoreceptor cells in retinas of Royal College of Surgeons (RCS) dystrophic rats for up to one year. In this study, we investigated the photoreceptor rescue effects in RCS rats within the first three weeks f...
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Veröffentlicht in: | Current eye research 1996-10, Vol.15 (10), p.1069-1077 |
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description | Purpose. We have previously shown that transplants of normal rat neonatal RPE cells rescued photoreceptor cells in retinas of Royal College of Surgeons (RCS) dystrophic rats for up to one year. In this study, we investigated the photoreceptor rescue effects in RCS rats within the first three weeks following transplantation in an attempt to determine if RPE transplants initiate repair mechanisms, specifically, outer segment (OS) regeneration.
Methods. Freshly isolated RPE cells from neonatal pigmented Long Evans rats were transplanted into the subretinal space of 22-23 day-old RCS rats using a transscleral approach. For controls, vehicle was similarly injected.
Results. When analyzed at 10 days post-transplantation, long inner segments were observed with short buds of outer segment growth in the area of the RPE-cell transplants. The outer segments were of insufficient length to be measured at 10 days, but by 14 and 21 days, OS were 2.02 ± 0.32 μm and 18.80 ± 2.78 μm, respectively. In vehicle-injected retinas from 10 to 21 days post-surgery, outer segments were not observed and the inner segments were three-fold shorter than in RPE-transplanted retinas. At 10 days post-transplantation, most RPE cells were seen in the sub-retinal space, but a few had attached to Bruch's membrane; however, by 21 days, many of the transplanted RPE cells had attached to Bruch's membrane, although a few were found free in the subretinal space.
Conclusions. This study has shown that transplants of normal rat neonatal RPE cells have the capacity to support not only photoreceptor cell survival but also initiate early repair mechanisms as exhibited by outer segment regeneration in RCS retinas. These results also conclusively show the important role that the RPE plays in outer segment growth and maturation. |
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Methods. Freshly isolated RPE cells from neonatal pigmented Long Evans rats were transplanted into the subretinal space of 22-23 day-old RCS rats using a transscleral approach. For controls, vehicle was similarly injected.
Results. When analyzed at 10 days post-transplantation, long inner segments were observed with short buds of outer segment growth in the area of the RPE-cell transplants. The outer segments were of insufficient length to be measured at 10 days, but by 14 and 21 days, OS were 2.02 ± 0.32 μm and 18.80 ± 2.78 μm, respectively. In vehicle-injected retinas from 10 to 21 days post-surgery, outer segments were not observed and the inner segments were three-fold shorter than in RPE-transplanted retinas. At 10 days post-transplantation, most RPE cells were seen in the sub-retinal space, but a few had attached to Bruch's membrane; however, by 21 days, many of the transplanted RPE cells had attached to Bruch's membrane, although a few were found free in the subretinal space.
Conclusions. This study has shown that transplants of normal rat neonatal RPE cells have the capacity to support not only photoreceptor cell survival but also initiate early repair mechanisms as exhibited by outer segment regeneration in RCS retinas. These results also conclusively show the important role that the RPE plays in outer segment growth and maturation.</description><identifier>ISSN: 0271-3683</identifier><identifier>EISSN: 1460-2202</identifier><identifier>DOI: 10.3109/02713689609017657</identifier><identifier>PMID: 8921247</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Animals ; Animals, Newborn ; Cell Survival ; Cell Transplantation ; Microscopy, Electron ; outer segment regeneration ; photo-receptor cell ; Photoreceptor Cells - physiology ; Photoreceptor Cells - ultrastructure ; Pigment Epithelium of Eye - cytology ; Pigment Epithelium of Eye - transplantation ; Pigment Epithelium of Eye - ultrastructure ; Rats ; Rats, Mutant Strains ; Regeneration - physiology ; Retinal Degeneration - pathology ; Retinal Degeneration - physiopathology ; Retinal Degeneration - surgery ; retinal pigment epithelium ; Rod Cell Outer Segment - physiology ; Rod Cell Outer Segment - ultrastructure ; Royal College of Surgeons rats ; transplantation</subject><ispartof>Current eye research, 1996-10, Vol.15 (10), p.1069-1077</ispartof><rights>1996 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1996</rights><rights>Copyright Swets & Zeitlinger bv Oct 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-44c46fc1330e77c875f73013b0953923239e6c91f2887dee20486746f312a2bc3</citedby><cites>FETCH-LOGICAL-c428t-44c46fc1330e77c875f73013b0953923239e6c91f2887dee20486746f312a2bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/02713689609017657$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/02713689609017657$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,59652,59758,60441,60547,61226,61261,61407,61442</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8921247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Ning</creatorcontrib><creatorcontrib>Fan, Wei</creatorcontrib><creatorcontrib>Sheedlo, Harold J.</creatorcontrib><creatorcontrib>Aschenbrenner, John E.</creatorcontrib><creatorcontrib>Turner, James E.</creatorcontrib><title>Photoreceptor repair in response to RPE transplants in RCS rats: Outer segment regeneration</title><title>Current eye research</title><addtitle>Curr Eye Res</addtitle><description>Purpose. We have previously shown that transplants of normal rat neonatal RPE cells rescued photoreceptor cells in retinas of Royal College of Surgeons (RCS) dystrophic rats for up to one year. In this study, we investigated the photoreceptor rescue effects in RCS rats within the first three weeks following transplantation in an attempt to determine if RPE transplants initiate repair mechanisms, specifically, outer segment (OS) regeneration.
Methods. Freshly isolated RPE cells from neonatal pigmented Long Evans rats were transplanted into the subretinal space of 22-23 day-old RCS rats using a transscleral approach. For controls, vehicle was similarly injected.
Results. When analyzed at 10 days post-transplantation, long inner segments were observed with short buds of outer segment growth in the area of the RPE-cell transplants. The outer segments were of insufficient length to be measured at 10 days, but by 14 and 21 days, OS were 2.02 ± 0.32 μm and 18.80 ± 2.78 μm, respectively. In vehicle-injected retinas from 10 to 21 days post-surgery, outer segments were not observed and the inner segments were three-fold shorter than in RPE-transplanted retinas. At 10 days post-transplantation, most RPE cells were seen in the sub-retinal space, but a few had attached to Bruch's membrane; however, by 21 days, many of the transplanted RPE cells had attached to Bruch's membrane, although a few were found free in the subretinal space.
Conclusions. This study has shown that transplants of normal rat neonatal RPE cells have the capacity to support not only photoreceptor cell survival but also initiate early repair mechanisms as exhibited by outer segment regeneration in RCS retinas. These results also conclusively show the important role that the RPE plays in outer segment growth and maturation.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Cell Survival</subject><subject>Cell Transplantation</subject><subject>Microscopy, Electron</subject><subject>outer segment regeneration</subject><subject>photo-receptor cell</subject><subject>Photoreceptor Cells - physiology</subject><subject>Photoreceptor Cells - ultrastructure</subject><subject>Pigment Epithelium of Eye - cytology</subject><subject>Pigment Epithelium of Eye - transplantation</subject><subject>Pigment Epithelium of Eye - ultrastructure</subject><subject>Rats</subject><subject>Rats, Mutant Strains</subject><subject>Regeneration - physiology</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal Degeneration - physiopathology</subject><subject>Retinal Degeneration - surgery</subject><subject>retinal pigment epithelium</subject><subject>Rod Cell Outer Segment - physiology</subject><subject>Rod Cell Outer Segment - ultrastructure</subject><subject>Royal College of Surgeons rats</subject><subject>transplantation</subject><issn>0271-3683</issn><issn>1460-2202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF9r2zAUxcVoSdNuH2APBdOHvXnVP1tSu5cR2q5QSEi7pz0YRblOXGzJlWRGv31lEsbWkacrdM7vcO9B6DPBXxnB6hJTQVgpVYkVJqIsxAc0JbzEOaWYHqHpqOfJwE7QaQjPGI8ffIImUlFCuZiiX4uti86DgT6NzEOvG581Nr1C72yALLpsubjJotc29K22MYzycvaYeR3DVTYfIvgswKYDGxO2AQtJaZz9iI5r3Qb4tJ9n6OftzdPsR_4wv7uffX_IDacy5pwbXtaGMIZBCCNFUQuGCVthVTBFGWUKSqNITaUUawCKuSxFQhihmq4MO0Nfdrm9dy8DhFh1TTDQpmXBDaESsuAFxyoZL94Zn93gbdqtIqqglJRSJBPZmYx3IXioq943nfavFcHV2Hr1X-uJOd8HD6sO1n-Ifc1J_7bTG1s73-nfzrfrKurX1vk6FWuaMEYfjr_-B9-CbuPWaA9_HXCQfgPzzKB7</recordid><startdate>19961001</startdate><enddate>19961001</enddate><creator>Lin, Ning</creator><creator>Fan, Wei</creator><creator>Sheedlo, Harold J.</creator><creator>Aschenbrenner, John E.</creator><creator>Turner, James E.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Swets & Zeitlinger bv</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>7X8</scope></search><sort><creationdate>19961001</creationdate><title>Photoreceptor repair in response to RPE transplants in RCS rats: Outer segment regeneration</title><author>Lin, Ning ; Fan, Wei ; Sheedlo, Harold J. ; Aschenbrenner, John E. ; Turner, James E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-44c46fc1330e77c875f73013b0953923239e6c91f2887dee20486746f312a2bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Cell Survival</topic><topic>Cell Transplantation</topic><topic>Microscopy, Electron</topic><topic>outer segment regeneration</topic><topic>photo-receptor cell</topic><topic>Photoreceptor Cells - physiology</topic><topic>Photoreceptor Cells - ultrastructure</topic><topic>Pigment Epithelium of Eye - cytology</topic><topic>Pigment Epithelium of Eye - transplantation</topic><topic>Pigment Epithelium of Eye - ultrastructure</topic><topic>Rats</topic><topic>Rats, Mutant Strains</topic><topic>Regeneration - physiology</topic><topic>Retinal Degeneration - pathology</topic><topic>Retinal Degeneration - physiopathology</topic><topic>Retinal Degeneration - surgery</topic><topic>retinal pigment epithelium</topic><topic>Rod Cell Outer Segment - physiology</topic><topic>Rod Cell Outer Segment - ultrastructure</topic><topic>Royal College of Surgeons rats</topic><topic>transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Ning</creatorcontrib><creatorcontrib>Fan, Wei</creatorcontrib><creatorcontrib>Sheedlo, Harold J.</creatorcontrib><creatorcontrib>Aschenbrenner, John E.</creatorcontrib><creatorcontrib>Turner, James E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Ning</au><au>Fan, Wei</au><au>Sheedlo, Harold J.</au><au>Aschenbrenner, John E.</au><au>Turner, James E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoreceptor repair in response to RPE transplants in RCS rats: Outer segment regeneration</atitle><jtitle>Current eye research</jtitle><addtitle>Curr Eye Res</addtitle><date>1996-10-01</date><risdate>1996</risdate><volume>15</volume><issue>10</issue><spage>1069</spage><epage>1077</epage><pages>1069-1077</pages><issn>0271-3683</issn><eissn>1460-2202</eissn><abstract>Purpose. We have previously shown that transplants of normal rat neonatal RPE cells rescued photoreceptor cells in retinas of Royal College of Surgeons (RCS) dystrophic rats for up to one year. In this study, we investigated the photoreceptor rescue effects in RCS rats within the first three weeks following transplantation in an attempt to determine if RPE transplants initiate repair mechanisms, specifically, outer segment (OS) regeneration.
Methods. Freshly isolated RPE cells from neonatal pigmented Long Evans rats were transplanted into the subretinal space of 22-23 day-old RCS rats using a transscleral approach. For controls, vehicle was similarly injected.
Results. When analyzed at 10 days post-transplantation, long inner segments were observed with short buds of outer segment growth in the area of the RPE-cell transplants. The outer segments were of insufficient length to be measured at 10 days, but by 14 and 21 days, OS were 2.02 ± 0.32 μm and 18.80 ± 2.78 μm, respectively. In vehicle-injected retinas from 10 to 21 days post-surgery, outer segments were not observed and the inner segments were three-fold shorter than in RPE-transplanted retinas. At 10 days post-transplantation, most RPE cells were seen in the sub-retinal space, but a few had attached to Bruch's membrane; however, by 21 days, many of the transplanted RPE cells had attached to Bruch's membrane, although a few were found free in the subretinal space.
Conclusions. This study has shown that transplants of normal rat neonatal RPE cells have the capacity to support not only photoreceptor cell survival but also initiate early repair mechanisms as exhibited by outer segment regeneration in RCS retinas. These results also conclusively show the important role that the RPE plays in outer segment growth and maturation.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>8921247</pmid><doi>10.3109/02713689609017657</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Animals, Newborn Cell Survival Cell Transplantation Microscopy, Electron outer segment regeneration photo-receptor cell Photoreceptor Cells - physiology Photoreceptor Cells - ultrastructure Pigment Epithelium of Eye - cytology Pigment Epithelium of Eye - transplantation Pigment Epithelium of Eye - ultrastructure Rats Rats, Mutant Strains Regeneration - physiology Retinal Degeneration - pathology Retinal Degeneration - physiopathology Retinal Degeneration - surgery retinal pigment epithelium Rod Cell Outer Segment - physiology Rod Cell Outer Segment - ultrastructure Royal College of Surgeons rats transplantation |
title | Photoreceptor repair in response to RPE transplants in RCS rats: Outer segment regeneration |
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