Upregulation of Semaphorin 3A and the associated biochemical and cellular events in a rat model of retinal detachment
Background Retinal detachment, as a result of injury or disease, is a severe disorder that may ultimately lead to complete blindness. Despite advanced surgical repair techniques, the visual acuity of patients is often limited. We investigated some of the biochemical and morphological alterations fol...
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description | Background
Retinal detachment, as a result of injury or disease, is a severe disorder that may ultimately lead to complete blindness. Despite advanced surgical repair techniques, the visual acuity of patients is often limited. We investigated some of the biochemical and morphological alterations following experimental retinal detachment in laboratory animals.
Methods
Unilateral retinal detachment was induced in male Wistar rats; contralateral untreated eyes served as a control. Approximately half of the retinal area was detached by a sub-retinal injection of 5 μl Saline. The incidence and extent of the retinal detachment was evaluated using MRI analysis and fundus images. The retinas were collected at intervals of 24 hours, 7, 14 and 28 days following the procedure. Using Western blot and immunohistochemical analysis, the expression levels of Semaphorin3A, Neuropilin1, GAP43 and NF-H were studied. In addition, morphological changes in Müller and microglial cells were examined. TUNEL staining was used to assess apoptosis.
Results
We found that the expression level of Semaphorin3A was up-regulated and reached its peak at two time points: 24 hours and 14 days after surgery. A similar pattern of expression was found for Neuropilin1. TUNEL-positive cells, indicating apoptotic processes, were evident 24 hours post retinal detachment and increased after 7 days. On the other hand, GAP43 expression was up-regulated 14 days after retinal detachment, and further intensified 28 days post-surgery. Microglial cells were activated shortly after detachment and concentrated mostly at the inner plexiform layer. GFAP staining revealed hypertrophy of Müller cells.
Conclusions
The biochemical and morphological changes suggest that apoptosis as well as axonal regrowth take place following retinal detachment. Collectively, these findings may explain the limited success following repair surgery in terms of visual acuity and physiological function of the retina. Our study may open a new approach for treatment of early phase retinal detachment, as well as improve post-operative care that may, in turn, improve the functional result of the surgery. In addition, further study is required on several other factors that may affect visual acuity, such as size and location of the detached area and the time lapse between detachment and surgery. |
doi_str_mv | 10.1007/s00417-008-0945-x |
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Retinal detachment, as a result of injury or disease, is a severe disorder that may ultimately lead to complete blindness. Despite advanced surgical repair techniques, the visual acuity of patients is often limited. We investigated some of the biochemical and morphological alterations following experimental retinal detachment in laboratory animals.
Methods
Unilateral retinal detachment was induced in male Wistar rats; contralateral untreated eyes served as a control. Approximately half of the retinal area was detached by a sub-retinal injection of 5 μl Saline. The incidence and extent of the retinal detachment was evaluated using MRI analysis and fundus images. The retinas were collected at intervals of 24 hours, 7, 14 and 28 days following the procedure. Using Western blot and immunohistochemical analysis, the expression levels of Semaphorin3A, Neuropilin1, GAP43 and NF-H were studied. In addition, morphological changes in Müller and microglial cells were examined. TUNEL staining was used to assess apoptosis.
Results
We found that the expression level of Semaphorin3A was up-regulated and reached its peak at two time points: 24 hours and 14 days after surgery. A similar pattern of expression was found for Neuropilin1. TUNEL-positive cells, indicating apoptotic processes, were evident 24 hours post retinal detachment and increased after 7 days. On the other hand, GAP43 expression was up-regulated 14 days after retinal detachment, and further intensified 28 days post-surgery. Microglial cells were activated shortly after detachment and concentrated mostly at the inner plexiform layer. GFAP staining revealed hypertrophy of Müller cells.
Conclusions
The biochemical and morphological changes suggest that apoptosis as well as axonal regrowth take place following retinal detachment. Collectively, these findings may explain the limited success following repair surgery in terms of visual acuity and physiological function of the retina. Our study may open a new approach for treatment of early phase retinal detachment, as well as improve post-operative care that may, in turn, improve the functional result of the surgery. In addition, further study is required on several other factors that may affect visual acuity, such as size and location of the detached area and the time lapse between detachment and surgery.</description><identifier>ISSN: 0721-832X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-008-0945-x</identifier><identifier>PMID: 18815803</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Apoptosis - physiology ; Axons - physiology ; Basic Science ; Blotting, Western ; C-Reactive Protein - metabolism ; Disease Models, Animal ; GAP-43 Protein - metabolism ; Glial Fibrillary Acidic Protein - metabolism ; Immunohistochemistry ; In Situ Nick-End Labeling ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine & Public Health ; Microglia - metabolism ; Microglia - pathology ; Nerve Regeneration - physiology ; Nerve Tissue Proteins - metabolism ; Ophthalmology ; Rats ; Rats, Wistar ; Retinal Detachment - metabolism ; Retinal Detachment - pathology ; Retinal Ganglion Cells - metabolism ; Retinal Ganglion Cells - pathology ; Semaphorin-3A - metabolism ; Up-Regulation - physiology</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2009, Vol.247 (1), p.73-86</ispartof><rights>Springer-Verlag 2008</rights><rights>Springer-Verlag 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-f24509f70b000d7c58e863ab3f6c3e49371ed097ddb4e76ac94c2d5d8267bad43</citedby><cites>FETCH-LOGICAL-c369t-f24509f70b000d7c58e863ab3f6c3e49371ed097ddb4e76ac94c2d5d8267bad43</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/s00417-008-0945-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00417-008-0945-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18815803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klebanov, Olga</creatorcontrib><creatorcontrib>Nitzan, Anat</creatorcontrib><creatorcontrib>Raz, Dorit</creatorcontrib><creatorcontrib>Barzilai, Ari</creatorcontrib><creatorcontrib>Solomon, Arieh S.</creatorcontrib><title>Upregulation of Semaphorin 3A and the associated biochemical and cellular events in a rat model of retinal detachment</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>Background
Retinal detachment, as a result of injury or disease, is a severe disorder that may ultimately lead to complete blindness. Despite advanced surgical repair techniques, the visual acuity of patients is often limited. We investigated some of the biochemical and morphological alterations following experimental retinal detachment in laboratory animals.
Methods
Unilateral retinal detachment was induced in male Wistar rats; contralateral untreated eyes served as a control. Approximately half of the retinal area was detached by a sub-retinal injection of 5 μl Saline. The incidence and extent of the retinal detachment was evaluated using MRI analysis and fundus images. The retinas were collected at intervals of 24 hours, 7, 14 and 28 days following the procedure. Using Western blot and immunohistochemical analysis, the expression levels of Semaphorin3A, Neuropilin1, GAP43 and NF-H were studied. In addition, morphological changes in Müller and microglial cells were examined. TUNEL staining was used to assess apoptosis.
Results
We found that the expression level of Semaphorin3A was up-regulated and reached its peak at two time points: 24 hours and 14 days after surgery. A similar pattern of expression was found for Neuropilin1. TUNEL-positive cells, indicating apoptotic processes, were evident 24 hours post retinal detachment and increased after 7 days. On the other hand, GAP43 expression was up-regulated 14 days after retinal detachment, and further intensified 28 days post-surgery. Microglial cells were activated shortly after detachment and concentrated mostly at the inner plexiform layer. GFAP staining revealed hypertrophy of Müller cells.
Conclusions
The biochemical and morphological changes suggest that apoptosis as well as axonal regrowth take place following retinal detachment. Collectively, these findings may explain the limited success following repair surgery in terms of visual acuity and physiological function of the retina. Our study may open a new approach for treatment of early phase retinal detachment, as well as improve post-operative care that may, in turn, improve the functional result of the surgery. In addition, further study is required on several other factors that may affect visual acuity, such as size and location of the detached area and the time lapse between detachment and surgery.</description><subject>Animals</subject><subject>Apoptosis - physiology</subject><subject>Axons - physiology</subject><subject>Basic Science</subject><subject>Blotting, Western</subject><subject>C-Reactive Protein - metabolism</subject><subject>Disease Models, Animal</subject><subject>GAP-43 Protein - metabolism</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Immunohistochemistry</subject><subject>In Situ Nick-End Labeling</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microglia - metabolism</subject><subject>Microglia - pathology</subject><subject>Nerve Regeneration - physiology</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Ophthalmology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Retinal Detachment - metabolism</subject><subject>Retinal Detachment - pathology</subject><subject>Retinal Ganglion Cells - metabolism</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Semaphorin-3A - metabolism</subject><subject>Up-Regulation - physiology</subject><issn>0721-832X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kUFL5DAYhsOirOPoD9jLEjx46_qlaZvmOAyrLgh70AFvIU2-OpW2GZN0cf-9qTMgCJ5y-J73zQsPIT8Y_GIA4ioAFExkAHUGsiiz129kwQpeZgLyxyOyAJGzrOb54wk5DeEZEs5L9p2csLpmZQ18QabNzuPT1OvYuZG6lt7joHdb57uR8hXVo6Vxi1SH4EynI1radM5sceiM7t_PBvs-5T3FfzjGQFNQU68jHZzFfq70GLsx0RajNtshUWfkuNV9wPPDuySb698P69vs7u_Nn_XqLjO8kjFr86IE2Qpo0nQrTFljXXHd8LYyHAvJBUMLUljbFCgqbWRhclvaOq9Eo23Bl-Ry37vz7mXCENXQhXmwHtFNQVWVYFKIGbz4BD67yafRQeUchGQSZILYHjLeheCxVTvfDdr_VwzULETthagkRM1C1GvK_DwUT82A9iNxMJCAfA-EdBqf0H_8_HXrGx05l3k</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Klebanov, Olga</creator><creator>Nitzan, Anat</creator><creator>Raz, Dorit</creator><creator>Barzilai, Ari</creator><creator>Solomon, Arieh S.</creator><general>Springer-Verlag</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>2009</creationdate><title>Upregulation of Semaphorin 3A and the associated biochemical and cellular events in a rat model of retinal detachment</title><author>Klebanov, Olga ; Nitzan, Anat ; Raz, Dorit ; Barzilai, Ari ; Solomon, Arieh S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-f24509f70b000d7c58e863ab3f6c3e49371ed097ddb4e76ac94c2d5d8267bad43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Apoptosis - physiology</topic><topic>Axons - physiology</topic><topic>Basic Science</topic><topic>Blotting, Western</topic><topic>C-Reactive Protein - metabolism</topic><topic>Disease Models, Animal</topic><topic>GAP-43 Protein - metabolism</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Immunohistochemistry</topic><topic>In Situ Nick-End Labeling</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Microglia - metabolism</topic><topic>Microglia - pathology</topic><topic>Nerve Regeneration - physiology</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Ophthalmology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Retinal Detachment - metabolism</topic><topic>Retinal Detachment - pathology</topic><topic>Retinal Ganglion Cells - metabolism</topic><topic>Retinal Ganglion Cells - pathology</topic><topic>Semaphorin-3A - metabolism</topic><topic>Up-Regulation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Klebanov, Olga</creatorcontrib><creatorcontrib>Nitzan, Anat</creatorcontrib><creatorcontrib>Raz, Dorit</creatorcontrib><creatorcontrib>Barzilai, Ari</creatorcontrib><creatorcontrib>Solomon, Arieh S.</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>Klebanov, Olga</au><au>Nitzan, Anat</au><au>Raz, Dorit</au><au>Barzilai, Ari</au><au>Solomon, Arieh S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upregulation of Semaphorin 3A and the associated biochemical and cellular events in a rat model of retinal detachment</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>2009</date><risdate>2009</risdate><volume>247</volume><issue>1</issue><spage>73</spage><epage>86</epage><pages>73-86</pages><issn>0721-832X</issn><eissn>1435-702X</eissn><abstract>Background
Retinal detachment, as a result of injury or disease, is a severe disorder that may ultimately lead to complete blindness. Despite advanced surgical repair techniques, the visual acuity of patients is often limited. We investigated some of the biochemical and morphological alterations following experimental retinal detachment in laboratory animals.
Methods
Unilateral retinal detachment was induced in male Wistar rats; contralateral untreated eyes served as a control. Approximately half of the retinal area was detached by a sub-retinal injection of 5 μl Saline. The incidence and extent of the retinal detachment was evaluated using MRI analysis and fundus images. The retinas were collected at intervals of 24 hours, 7, 14 and 28 days following the procedure. Using Western blot and immunohistochemical analysis, the expression levels of Semaphorin3A, Neuropilin1, GAP43 and NF-H were studied. In addition, morphological changes in Müller and microglial cells were examined. TUNEL staining was used to assess apoptosis.
Results
We found that the expression level of Semaphorin3A was up-regulated and reached its peak at two time points: 24 hours and 14 days after surgery. A similar pattern of expression was found for Neuropilin1. TUNEL-positive cells, indicating apoptotic processes, were evident 24 hours post retinal detachment and increased after 7 days. On the other hand, GAP43 expression was up-regulated 14 days after retinal detachment, and further intensified 28 days post-surgery. Microglial cells were activated shortly after detachment and concentrated mostly at the inner plexiform layer. GFAP staining revealed hypertrophy of Müller cells.
Conclusions
The biochemical and morphological changes suggest that apoptosis as well as axonal regrowth take place following retinal detachment. Collectively, these findings may explain the limited success following repair surgery in terms of visual acuity and physiological function of the retina. Our study may open a new approach for treatment of early phase retinal detachment, as well as improve post-operative care that may, in turn, improve the functional result of the surgery. In addition, further study is required on several other factors that may affect visual acuity, such as size and location of the detached area and the time lapse between detachment and surgery.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18815803</pmid><doi>10.1007/s00417-008-0945-x</doi><tpages>14</tpages></addata></record> |
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subjects | Animals Apoptosis - physiology Axons - physiology Basic Science Blotting, Western C-Reactive Protein - metabolism Disease Models, Animal GAP-43 Protein - metabolism Glial Fibrillary Acidic Protein - metabolism Immunohistochemistry In Situ Nick-End Labeling Magnetic Resonance Imaging Male Medicine Medicine & Public Health Microglia - metabolism Microglia - pathology Nerve Regeneration - physiology Nerve Tissue Proteins - metabolism Ophthalmology Rats Rats, Wistar Retinal Detachment - metabolism Retinal Detachment - pathology Retinal Ganglion Cells - metabolism Retinal Ganglion Cells - pathology Semaphorin-3A - metabolism Up-Regulation - physiology |
title | Upregulation of Semaphorin 3A and the associated biochemical and cellular events in a rat model of retinal detachment |
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