Retinal vasculature changes in Norrie disease mice
To correlate morphologic changes in the retinal vasculature with degenerative changes in the neuronal retina of mice lacking 56 amino acids from the N-terminus of the Norrie disease (ND) gene product. Posterior eye segments of ND mice of different age groups were investigated by light and electron m...
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Veröffentlicht in: | Investigative ophthalmology & visual science 1998-11, Vol.39 (12), p.2450-2457 |
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creator | Richter, M Gottanka, J May, CA Welge-Lussen, U Berger, W Lutjen-Drecoll, E |
description | To correlate morphologic changes in the retinal vasculature with degenerative changes in the neuronal retina of mice lacking 56 amino acids from the N-terminus of the Norrie disease (ND) gene product.
Posterior eye segments of ND mice of different age groups were investigated by light and electron microscopy (EM) and scanning EM of vascular corrosion cast preparations. The results were qualitatively and quantitatively compared with those obtained in age-matched littermate control mice and C57B1/6 mice.
Quantitative evaluation revealed an increase in the number of blood vessels in the interface of the ganglion cell layer and the nerve fiber layer and a decrease in the inner and outer plexiform layers in ND mice older than 9 days compared with control mice. Vessels were also seen adjacent to the vitreous surface of the inner limiting membrane. Most of these vessels showed fenestrations and occasionally penetrated the inner limiting membrane. Hyaloid vessels were still present in the vitreous. The abnormal vascularization pattern was found in the entire retina and occurred in addition to the previously described alterations of the neuronal retina.
There is a malformation of the retinal vasculature and a persistence of hyaloid vessels in the vitreous of ND mice. It is assumed that the ND gene product is required for normal vascularization of the inner retinal layers and for atrophy of hyaloid vessels. |
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Posterior eye segments of ND mice of different age groups were investigated by light and electron microscopy (EM) and scanning EM of vascular corrosion cast preparations. The results were qualitatively and quantitatively compared with those obtained in age-matched littermate control mice and C57B1/6 mice.
Quantitative evaluation revealed an increase in the number of blood vessels in the interface of the ganglion cell layer and the nerve fiber layer and a decrease in the inner and outer plexiform layers in ND mice older than 9 days compared with control mice. Vessels were also seen adjacent to the vitreous surface of the inner limiting membrane. Most of these vessels showed fenestrations and occasionally penetrated the inner limiting membrane. Hyaloid vessels were still present in the vitreous. The abnormal vascularization pattern was found in the entire retina and occurred in addition to the previously described alterations of the neuronal retina.
There is a malformation of the retinal vasculature and a persistence of hyaloid vessels in the vitreous of ND mice. It is assumed that the ND gene product is required for normal vascularization of the inner retinal layers and for atrophy of hyaloid vessels.</description><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>PMID: 9804153</identifier><identifier>CODEN: IOVSDA</identifier><language>eng</language><publisher>Rockville, MD: ARVO</publisher><subject>Animals ; Biological and medical sciences ; Blindness - genetics ; Blindness - pathology ; Corrosion Casting ; Eye Proteins - genetics ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Microscopy, Electron, Scanning ; Nerve Tissue Proteins - genetics ; Ophthalmology ; Retinal Degeneration - genetics ; Retinal Degeneration - pathology ; Retinal Vessels - pathology ; Retinal Vessels - ultrastructure ; Retinopathies</subject><ispartof>Investigative ophthalmology & visual science, 1998-11, Vol.39 (12), p.2450-2457</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1596282$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9804153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Richter, M</creatorcontrib><creatorcontrib>Gottanka, J</creatorcontrib><creatorcontrib>May, CA</creatorcontrib><creatorcontrib>Welge-Lussen, U</creatorcontrib><creatorcontrib>Berger, W</creatorcontrib><creatorcontrib>Lutjen-Drecoll, E</creatorcontrib><title>Retinal vasculature changes in Norrie disease mice</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>To correlate morphologic changes in the retinal vasculature with degenerative changes in the neuronal retina of mice lacking 56 amino acids from the N-terminus of the Norrie disease (ND) gene product.
Posterior eye segments of ND mice of different age groups were investigated by light and electron microscopy (EM) and scanning EM of vascular corrosion cast preparations. The results were qualitatively and quantitatively compared with those obtained in age-matched littermate control mice and C57B1/6 mice.
Quantitative evaluation revealed an increase in the number of blood vessels in the interface of the ganglion cell layer and the nerve fiber layer and a decrease in the inner and outer plexiform layers in ND mice older than 9 days compared with control mice. Vessels were also seen adjacent to the vitreous surface of the inner limiting membrane. Most of these vessels showed fenestrations and occasionally penetrated the inner limiting membrane. Hyaloid vessels were still present in the vitreous. The abnormal vascularization pattern was found in the entire retina and occurred in addition to the previously described alterations of the neuronal retina.
There is a malformation of the retinal vasculature and a persistence of hyaloid vessels in the vitreous of ND mice. It is assumed that the ND gene product is required for normal vascularization of the inner retinal layers and for atrophy of hyaloid vessels.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blindness - genetics</subject><subject>Blindness - pathology</subject><subject>Corrosion Casting</subject><subject>Eye Proteins - genetics</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron, Scanning</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Ophthalmology</subject><subject>Retinal Degeneration - genetics</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal Vessels - pathology</subject><subject>Retinal Vessels - ultrastructure</subject><subject>Retinopathies</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j81KxDAURoMo4zj6CEIXoqtCfpqkWcqgozAoiK7DbXs7jaSdMWktvr2VKa6-xXc4cE7IkknJU6lzcUqWlGUqpRnNzslFjJ-UcsY4XZCFyWnGpFgS_oa968An3xDLwUM_BEzKBrodxsR1ycs-BIdJ5SJCxKR1JV6Ssxp8xKt5V-Tj8eF9_ZRuXzfP6_tt2nCl-zRHVtUSOAikBSqjtSoQkRvUXDEmOSheK12D1qWhULFC5VRqYXJTlVktxIrcHr2HsP8aMPa2dbFE76HD_RCtnnK4MnwCr2dwKFqs7CG4FsKPnSOn_2b-p0bwdYCudPEfY9Ionv9p7o5Y43bN6ALa2IL3k5TZcRyFsYxbnkkqfgGL3GeR</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>Richter, M</creator><creator>Gottanka, J</creator><creator>May, CA</creator><creator>Welge-Lussen, U</creator><creator>Berger, W</creator><creator>Lutjen-Drecoll, E</creator><general>ARVO</general><general>Association for Research in Vision and Ophtalmology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19981101</creationdate><title>Retinal vasculature changes in Norrie disease mice</title><author>Richter, M ; Gottanka, J ; May, CA ; Welge-Lussen, U ; Berger, W ; Lutjen-Drecoll, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h267t-8e1df5a2a3e0be69776beee29e7261152a62f67fa77c90ad1b680573989dc4f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blindness - genetics</topic><topic>Blindness - pathology</topic><topic>Corrosion Casting</topic><topic>Eye Proteins - genetics</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Electron, Scanning</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Ophthalmology</topic><topic>Retinal Degeneration - genetics</topic><topic>Retinal Degeneration - pathology</topic><topic>Retinal Vessels - pathology</topic><topic>Retinal Vessels - ultrastructure</topic><topic>Retinopathies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Richter, M</creatorcontrib><creatorcontrib>Gottanka, J</creatorcontrib><creatorcontrib>May, CA</creatorcontrib><creatorcontrib>Welge-Lussen, U</creatorcontrib><creatorcontrib>Berger, W</creatorcontrib><creatorcontrib>Lutjen-Drecoll, E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Richter, M</au><au>Gottanka, J</au><au>May, CA</au><au>Welge-Lussen, U</au><au>Berger, W</au><au>Lutjen-Drecoll, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinal vasculature changes in Norrie disease mice</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>1998-11-01</date><risdate>1998</risdate><volume>39</volume><issue>12</issue><spage>2450</spage><epage>2457</epage><pages>2450-2457</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>To correlate morphologic changes in the retinal vasculature with degenerative changes in the neuronal retina of mice lacking 56 amino acids from the N-terminus of the Norrie disease (ND) gene product.
Posterior eye segments of ND mice of different age groups were investigated by light and electron microscopy (EM) and scanning EM of vascular corrosion cast preparations. The results were qualitatively and quantitatively compared with those obtained in age-matched littermate control mice and C57B1/6 mice.
Quantitative evaluation revealed an increase in the number of blood vessels in the interface of the ganglion cell layer and the nerve fiber layer and a decrease in the inner and outer plexiform layers in ND mice older than 9 days compared with control mice. Vessels were also seen adjacent to the vitreous surface of the inner limiting membrane. Most of these vessels showed fenestrations and occasionally penetrated the inner limiting membrane. Hyaloid vessels were still present in the vitreous. The abnormal vascularization pattern was found in the entire retina and occurred in addition to the previously described alterations of the neuronal retina.
There is a malformation of the retinal vasculature and a persistence of hyaloid vessels in the vitreous of ND mice. It is assumed that the ND gene product is required for normal vascularization of the inner retinal layers and for atrophy of hyaloid vessels.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>9804153</pmid><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Biological and medical sciences Blindness - genetics Blindness - pathology Corrosion Casting Eye Proteins - genetics Medical sciences Mice Mice, Inbred C57BL Microscopy, Electron, Scanning Nerve Tissue Proteins - genetics Ophthalmology Retinal Degeneration - genetics Retinal Degeneration - pathology Retinal Vessels - pathology Retinal Vessels - ultrastructure Retinopathies |
title | Retinal vasculature changes in Norrie disease mice |
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