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
Hauptverfasser: Richter, M, Gottanka, J, May, CA, Welge-Lussen, U, Berger, W, Lutjen-Drecoll, E
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container_end_page 2457
container_issue 12
container_start_page 2450
container_title Investigative ophthalmology & visual science
container_volume 39
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 &amp; 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&amp;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 &amp; 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 &amp; 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 &amp; 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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