Quantitative evaluation of the corneal endothelium in the mouse after grafting
Background/aim: Corneal graft survival depends critically on the quality of the endothelium. In this study the authors aimed to evaluate corneal endothelium in mice at different times after transplantation and to correlate endothelial integrity with corneal graft survival. Methods: Syngeneic and all...
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Veröffentlicht in: | British journal of ophthalmology 2004-09, Vol.88 (9), p.1209-1216 |
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description | Background/aim: Corneal graft survival depends critically on the quality of the endothelium. In this study the authors aimed to evaluate corneal endothelium in mice at different times after transplantation and to correlate endothelial integrity with corneal graft survival. Methods: Syngeneic and allogeneic corneal grafts at various times (days 0–60) after engraftment were examined in flat mount preparation by confocal microscopy, by evaluating the hexagonal pattern of the endothelial monolayer using actin staining of the cell cortex. Corneas from untreated mice and from mice, who were grafted after removal of draining lymph nodes served as controls. Results: In control corneas, more than 90% of the posterior surface was covered by endothelium. Syngeneic grafts were always covered by 54–99% of endothelium. In contrast, the posterior surface of corneal allografts showed great variation in the degree of endothelial cell coverage (0–98%). In addition, clinical opacity grading measure was not a reliable predictor of endothelial coverage. Conclusion: In corneal allografts there is progressive loss of endothelium over time, unlike with syngeneic grafts. However, in the early stages of allograft rejection, the grade of graft opacity does not accurately reflect the degree of endothelial cell coverage. Although corneal opacity grade is considered the main determinant of graft rejection, the data suggest that both the grade of corneal opacity plus a sufficient post-graft time duration (>8 weeks in the mouse) are required for the diagnosis of irreversible graft rejection. |
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In this study the authors aimed to evaluate corneal endothelium in mice at different times after transplantation and to correlate endothelial integrity with corneal graft survival. Methods: Syngeneic and allogeneic corneal grafts at various times (days 0–60) after engraftment were examined in flat mount preparation by confocal microscopy, by evaluating the hexagonal pattern of the endothelial monolayer using actin staining of the cell cortex. Corneas from untreated mice and from mice, who were grafted after removal of draining lymph nodes served as controls. Results: In control corneas, more than 90% of the posterior surface was covered by endothelium. Syngeneic grafts were always covered by 54–99% of endothelium. In contrast, the posterior surface of corneal allografts showed great variation in the degree of endothelial cell coverage (0–98%). In addition, clinical opacity grading measure was not a reliable predictor of endothelial coverage. Conclusion: In corneal allografts there is progressive loss of endothelium over time, unlike with syngeneic grafts. However, in the early stages of allograft rejection, the grade of graft opacity does not accurately reflect the degree of endothelial cell coverage. Although corneal opacity grade is considered the main determinant of graft rejection, the data suggest that both the grade of corneal opacity plus a sufficient post-graft time duration (>8 weeks in the mouse) are required for the diagnosis of irreversible graft rejection.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.2003.038703</identifier><identifier>PMID: 15317718</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>actin ; Animals ; Antibiotics ; Biological and medical sciences ; Cell Death - physiology ; Cell growth ; Colleges & universities ; confocal microscopy ; Cornea ; corneal endothelial cells ; Corneal Opacity - pathology ; corneal transplantation ; Corneal Transplantation - methods ; Diseases of cornea, anterior segment and sclera ; eGFP ; Endothelial Cells - pathology ; Endothelium ; Endothelium, Corneal - pathology ; enhanced green fluorescence protein ; Female ; Graft Survival - physiology ; Immunohistochemistry - methods ; Laboratory Science - Extended Reports ; LNR ; Lymph Node Excision ; lymph node removal ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Microscopy, Confocal - methods ; Molecular weight ; Ophthalmology ; paraformaldehyde ; PBS ; PFA ; phosphate buffered saline ; Rodents ; tissue plasminogen activator ; tPA ; Transplantation, Autologous ; Transplantation, Isogeneic ; Transplants & implants</subject><ispartof>British journal of ophthalmology, 2004-09, Vol.88 (9), p.1209-1216</ispartof><rights>Copyright 2004 British Journal of Ophthalmology</rights><rights>2004 INIST-CNRS</rights><rights>Copyright: 2004 Copyright 2004 British Journal of Ophthalmology</rights><rights>Copyright © Copyright 2004 British Journal of Ophthalmology 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b586t-2ae7ed34cd6c7a924382bd9807beb6af05a6c694b2cdd0f5bd1f74b4e7edebf53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1772317/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1772317/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16060733$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15317718$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Plskova, J</creatorcontrib><creatorcontrib>Kuffova, L</creatorcontrib><creatorcontrib>Filipec, M</creatorcontrib><creatorcontrib>Holan, V</creatorcontrib><creatorcontrib>Forrester, J V</creatorcontrib><title>Quantitative evaluation of the corneal endothelium in the mouse after grafting</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>Background/aim: Corneal graft survival depends critically on the quality of the endothelium. In this study the authors aimed to evaluate corneal endothelium in mice at different times after transplantation and to correlate endothelial integrity with corneal graft survival. Methods: Syngeneic and allogeneic corneal grafts at various times (days 0–60) after engraftment were examined in flat mount preparation by confocal microscopy, by evaluating the hexagonal pattern of the endothelial monolayer using actin staining of the cell cortex. Corneas from untreated mice and from mice, who were grafted after removal of draining lymph nodes served as controls. Results: In control corneas, more than 90% of the posterior surface was covered by endothelium. Syngeneic grafts were always covered by 54–99% of endothelium. In contrast, the posterior surface of corneal allografts showed great variation in the degree of endothelial cell coverage (0–98%). In addition, clinical opacity grading measure was not a reliable predictor of endothelial coverage. Conclusion: In corneal allografts there is progressive loss of endothelium over time, unlike with syngeneic grafts. However, in the early stages of allograft rejection, the grade of graft opacity does not accurately reflect the degree of endothelial cell coverage. Although corneal opacity grade is considered the main determinant of graft rejection, the data suggest that both the grade of corneal opacity plus a sufficient post-graft time duration (>8 weeks in the mouse) are required for the diagnosis of irreversible graft rejection.</description><subject>actin</subject><subject>Animals</subject><subject>Antibiotics</subject><subject>Biological and medical sciences</subject><subject>Cell Death - physiology</subject><subject>Cell growth</subject><subject>Colleges & universities</subject><subject>confocal microscopy</subject><subject>Cornea</subject><subject>corneal endothelial cells</subject><subject>Corneal Opacity - pathology</subject><subject>corneal transplantation</subject><subject>Corneal Transplantation - methods</subject><subject>Diseases of cornea, anterior segment and sclera</subject><subject>eGFP</subject><subject>Endothelial Cells - pathology</subject><subject>Endothelium</subject><subject>Endothelium, Corneal - pathology</subject><subject>enhanced green fluorescence protein</subject><subject>Female</subject><subject>Graft Survival - physiology</subject><subject>Immunohistochemistry - methods</subject><subject>Laboratory Science - Extended Reports</subject><subject>LNR</subject><subject>Lymph Node Excision</subject><subject>lymph node removal</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Confocal - methods</subject><subject>Molecular weight</subject><subject>Ophthalmology</subject><subject>paraformaldehyde</subject><subject>PBS</subject><subject>PFA</subject><subject>phosphate buffered saline</subject><subject>Rodents</subject><subject>tissue plasminogen activator</subject><subject>tPA</subject><subject>Transplantation, Autologous</subject><subject>Transplantation, Isogeneic</subject><subject>Transplants & implants</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkc1v1DAQxS0EotvCmRuKhOBQKVs7TmznUomuKEVqFyEBV8t2JlsviV3sZFX--zpk1Q8unGZG85uneXoIvSF4SQhlJ3rrlwXGdImp4Jg-QwtSMpEXmNfP0QJjzHNCGDlAhzFu01gwwl-iA1JRwjkRC7T-Nio32EENdgcZ7FQ3pta7zLfZcA2Z8cGB6jJwjU9zZ8c-s-7vqvdjhEy1A4RsE1K1bvMKvWhVF-H1vh6hH-efvq8u8suvn7-sPl7muhJsyAsFHBpamoYZruqipKLQTS0w16CZanGlmGF1qQvTNLitdENaXupyugLdVvQInc66N6PuoTHghqA6eRNsr8If6ZWVTzfOXsuN38lku0jek8CHvUDwv0eIg-xtNNB1ykHyJRnjteBcJPDdP-DWj8Elc5OWqAkpRJ2ok5kywccYoL1_hWA5JSVTUnJKSs5JpYu3jx088PtoEvB-D6hoVNcG5YyNDxzDDHM6CeUzZ-MAt_d7FX5Jximv5PrnSq6vyquzi_MzOb16PPO63_73yztEwLpr</recordid><startdate>20040901</startdate><enddate>20040901</enddate><creator>Plskova, J</creator><creator>Kuffova, L</creator><creator>Filipec, M</creator><creator>Holan, V</creator><creator>Forrester, J V</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>Copyright 2004 British Journal of Ophthalmology</general><scope>BSCLL</scope><scope>IQODW</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>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20040901</creationdate><title>Quantitative evaluation of the corneal endothelium in the mouse after grafting</title><author>Plskova, J ; Kuffova, L ; Filipec, M ; Holan, V ; Forrester, J V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b586t-2ae7ed34cd6c7a924382bd9807beb6af05a6c694b2cdd0f5bd1f74b4e7edebf53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>actin</topic><topic>Animals</topic><topic>Antibiotics</topic><topic>Biological and medical sciences</topic><topic>Cell Death - physiology</topic><topic>Cell growth</topic><topic>Colleges & universities</topic><topic>confocal microscopy</topic><topic>Cornea</topic><topic>corneal endothelial cells</topic><topic>Corneal Opacity - pathology</topic><topic>corneal transplantation</topic><topic>Corneal Transplantation - methods</topic><topic>Diseases of cornea, anterior segment and sclera</topic><topic>eGFP</topic><topic>Endothelial Cells - pathology</topic><topic>Endothelium</topic><topic>Endothelium, Corneal - pathology</topic><topic>enhanced green fluorescence protein</topic><topic>Female</topic><topic>Graft Survival - physiology</topic><topic>Immunohistochemistry - methods</topic><topic>Laboratory Science - Extended Reports</topic><topic>LNR</topic><topic>Lymph Node Excision</topic><topic>lymph node removal</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Confocal - methods</topic><topic>Molecular weight</topic><topic>Ophthalmology</topic><topic>paraformaldehyde</topic><topic>PBS</topic><topic>PFA</topic><topic>phosphate buffered saline</topic><topic>Rodents</topic><topic>tissue plasminogen activator</topic><topic>tPA</topic><topic>Transplantation, Autologous</topic><topic>Transplantation, Isogeneic</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Plskova, J</creatorcontrib><creatorcontrib>Kuffova, L</creatorcontrib><creatorcontrib>Filipec, M</creatorcontrib><creatorcontrib>Holan, V</creatorcontrib><creatorcontrib>Forrester, J V</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</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>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Plskova, J</au><au>Kuffova, L</au><au>Filipec, M</au><au>Holan, V</au><au>Forrester, J V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative evaluation of the corneal endothelium in the mouse after grafting</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>2004-09-01</date><risdate>2004</risdate><volume>88</volume><issue>9</issue><spage>1209</spage><epage>1216</epage><pages>1209-1216</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>Background/aim: Corneal graft survival depends critically on the quality of the endothelium. In this study the authors aimed to evaluate corneal endothelium in mice at different times after transplantation and to correlate endothelial integrity with corneal graft survival. Methods: Syngeneic and allogeneic corneal grafts at various times (days 0–60) after engraftment were examined in flat mount preparation by confocal microscopy, by evaluating the hexagonal pattern of the endothelial monolayer using actin staining of the cell cortex. Corneas from untreated mice and from mice, who were grafted after removal of draining lymph nodes served as controls. Results: In control corneas, more than 90% of the posterior surface was covered by endothelium. Syngeneic grafts were always covered by 54–99% of endothelium. In contrast, the posterior surface of corneal allografts showed great variation in the degree of endothelial cell coverage (0–98%). In addition, clinical opacity grading measure was not a reliable predictor of endothelial coverage. Conclusion: In corneal allografts there is progressive loss of endothelium over time, unlike with syngeneic grafts. However, in the early stages of allograft rejection, the grade of graft opacity does not accurately reflect the degree of endothelial cell coverage. Although corneal opacity grade is considered the main determinant of graft rejection, the data suggest that both the grade of corneal opacity plus a sufficient post-graft time duration (>8 weeks in the mouse) are required for the diagnosis of irreversible graft rejection.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>15317718</pmid><doi>10.1136/bjo.2003.038703</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | actin Animals Antibiotics Biological and medical sciences Cell Death - physiology Cell growth Colleges & universities confocal microscopy Cornea corneal endothelial cells Corneal Opacity - pathology corneal transplantation Corneal Transplantation - methods Diseases of cornea, anterior segment and sclera eGFP Endothelial Cells - pathology Endothelium Endothelium, Corneal - pathology enhanced green fluorescence protein Female Graft Survival - physiology Immunohistochemistry - methods Laboratory Science - Extended Reports LNR Lymph Node Excision lymph node removal Male Medical sciences Mice Mice, Inbred BALB C Mice, Inbred C57BL Microscopy, Confocal - methods Molecular weight Ophthalmology paraformaldehyde PBS PFA phosphate buffered saline Rodents tissue plasminogen activator tPA Transplantation, Autologous Transplantation, Isogeneic Transplants & implants |
title | Quantitative evaluation of the corneal endothelium in the mouse after grafting |
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