The Requirement of Pax6 for Postnatal Eye Development: Evidence from Experimental Mouse Chimeras

The small eye mouse mutant (Sey) is caused by a mutation of the Pax6 gene. Previous studies, in which aggregation chimeras were used, have demonstrated that Sey/Sey cells contribute poorly to the neural retina forming small clumps of cells restricted to the inner retina at embryonic day 16.5. In add...

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Veröffentlicht in:Investigative ophthalmology & visual science 2007-07, Vol.48 (7), p.3292-3300
Hauptverfasser: Li, Shengxiu, Goldowitz, Dan, Swanson, Douglas J
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Goldowitz, Dan
Swanson, Douglas J
description The small eye mouse mutant (Sey) is caused by a mutation of the Pax6 gene. Previous studies, in which aggregation chimeras were used, have demonstrated that Sey/Sey cells contribute poorly to the neural retina forming small clumps of cells restricted to the inner retina at embryonic day 16.5. In addition, Sey/+ cells are absent from the lens epithelium during this embryonic period and postnatally. This study was conducted to determine the fates of these Sey/Sey and Sey/+ cells with continued development in chimeric mouse eyes. Observations were made on heterozygous and homozygous Sey cells in chimeric eyes from postnatal day (P)0 to P10. In Sey/Seywild-type (wt) chimeras, all Sey/Sey cells originating from retinal progenitor cells died at perinatal times. The only remaining Sey/Sey cells in the neural retina were associated with blood vessels, including vascular endothelial cells, pericytes, astrocytes, and microglia, which have extraretinal origins. In contrast, Sey/+ cells formed all retinal cell classes. As previously reported, Sey/Sey cells were absent from the lens and corneal epithelium. However, in contrast to previous reports, Sey/+ cells contributed to the lens epithelium as well as corneal tissues, and Sey/Sey cells were absent from the anterior retinal pigment epithelium. All evidence showed that, when Pax6 is absent at the initial stages of the development, Sey/Sey cells that contribute to the neural retina die, even when wild-type cells are available to provide normal environmental cues.
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Previous studies, in which aggregation chimeras were used, have demonstrated that Sey/Sey cells contribute poorly to the neural retina forming small clumps of cells restricted to the inner retina at embryonic day 16.5. In addition, Sey/+ cells are absent from the lens epithelium during this embryonic period and postnatally. This study was conducted to determine the fates of these Sey/Sey and Sey/+ cells with continued development in chimeric mouse eyes. Observations were made on heterozygous and homozygous Sey cells in chimeric eyes from postnatal day (P)0 to P10. In Sey/Sey&lt;--&gt;wild-type (wt) chimeras, all Sey/Sey cells originating from retinal progenitor cells died at perinatal times. The only remaining Sey/Sey cells in the neural retina were associated with blood vessels, including vascular endothelial cells, pericytes, astrocytes, and microglia, which have extraretinal origins. In contrast, Sey/+ cells formed all retinal cell classes. As previously reported, Sey/Sey cells were absent from the lens and corneal epithelium. However, in contrast to previous reports, Sey/+ cells contributed to the lens epithelium as well as corneal tissues, and Sey/Sey cells were absent from the anterior retinal pigment epithelium. 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Previous studies, in which aggregation chimeras were used, have demonstrated that Sey/Sey cells contribute poorly to the neural retina forming small clumps of cells restricted to the inner retina at embryonic day 16.5. In addition, Sey/+ cells are absent from the lens epithelium during this embryonic period and postnatally. This study was conducted to determine the fates of these Sey/Sey and Sey/+ cells with continued development in chimeric mouse eyes. Observations were made on heterozygous and homozygous Sey cells in chimeric eyes from postnatal day (P)0 to P10. In Sey/Sey&lt;--&gt;wild-type (wt) chimeras, all Sey/Sey cells originating from retinal progenitor cells died at perinatal times. The only remaining Sey/Sey cells in the neural retina were associated with blood vessels, including vascular endothelial cells, pericytes, astrocytes, and microglia, which have extraretinal origins. In contrast, Sey/+ cells formed all retinal cell classes. As previously reported, Sey/Sey cells were absent from the lens and corneal epithelium. However, in contrast to previous reports, Sey/+ cells contributed to the lens epithelium as well as corneal tissues, and Sey/Sey cells were absent from the anterior retinal pigment epithelium. All evidence showed that, when Pax6 is absent at the initial stages of the development, Sey/Sey cells that contribute to the neural retina die, even when wild-type cells are available to provide normal environmental cues.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chimera - genetics</subject><subject>Chimera - metabolism</subject><subject>Epithelium, Corneal - embryology</subject><subject>Epithelium, Corneal - metabolism</subject><subject>Eye - embryology</subject><subject>Eye - metabolism</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Eye Proteins - physiology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Developmental - physiology</subject><subject>Genotype</subject><subject>Homeodomain Proteins - physiology</subject><subject>Immunoenzyme Techniques</subject><subject>Iris - embryology</subject><subject>Iris - metabolism</subject><subject>Lens, Crystalline - embryology</subject><subject>Lens, Crystalline - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Microphthalmos - genetics</subject><subject>Microphthalmos - metabolism</subject><subject>Microphthalmos - pathology</subject><subject>Paired Box Transcription Factors - physiology</subject><subject>PAX6 Transcription Factor</subject><subject>Phenotype</subject><subject>Pigment Epithelium of Eye - metabolism</subject><subject>Polymerase Chain Reaction</subject><subject>Repressor Proteins - physiology</subject><subject>Retina - embryology</subject><subject>Retina - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0146-0404</issn><issn>1552-5783</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0M1r2zAYBnAxOtas223nokt7mjt9S-6tZNkHdKyM7qzJ8qvGxbZSyUna_34yDeQkXvTj4eFB6BMlV5Qq_aWLu3xFVEWFYW_QgkrJKqkNP0ELQoWqiCDiFL3P-ZEQRikj79Ap1bKmNaEL9O9-DfgPPG27BAOME44B37lnhUNM-C7maXST6_HqBfBX2EEfN7O6xqtd18LoAYcUB7x63kDq5p9if8VtBrxclzu5_AG9Da7P8PHwnqG_31b3yx_V7e_vP5c3t5XnkkyV0Z40gtZcSmUEY8a74CUXdd0qIVrNHXFeB-BSOCJYLUljPHeGyabhrQz8DF2-5m5SfNpCnuzQZQ9970YohawmSlHKWYGfX6FPMecEwW5KdZdeLCV2XtTOi1qi7Lxo4eeH3G0zQHvEhwkLuDgAl73rQ3Kj7_LRGVNrZdSx4Lp7WO_L3DYPru9LLLX7_V4Yqy1nNeP_AfXMi7I</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Li, Shengxiu</creator><creator>Goldowitz, Dan</creator><creator>Swanson, Douglas J</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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070701</creationdate><title>The Requirement of Pax6 for Postnatal Eye Development: Evidence from Experimental Mouse Chimeras</title><author>Li, Shengxiu ; Goldowitz, Dan ; Swanson, Douglas J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-87c0b419355684228cafc53499d644d73a0ac7fe354a042950b8c3a825bb3d5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chimera - genetics</topic><topic>Chimera - metabolism</topic><topic>Epithelium, Corneal - embryology</topic><topic>Epithelium, Corneal - metabolism</topic><topic>Eye - embryology</topic><topic>Eye - metabolism</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Eye Proteins - physiology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Developmental - physiology</topic><topic>Genotype</topic><topic>Homeodomain Proteins - physiology</topic><topic>Immunoenzyme Techniques</topic><topic>Iris - embryology</topic><topic>Iris - metabolism</topic><topic>Lens, Crystalline - embryology</topic><topic>Lens, Crystalline - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Microphthalmos - genetics</topic><topic>Microphthalmos - metabolism</topic><topic>Microphthalmos - pathology</topic><topic>Paired Box Transcription Factors - physiology</topic><topic>PAX6 Transcription Factor</topic><topic>Phenotype</topic><topic>Pigment Epithelium of Eye - metabolism</topic><topic>Polymerase Chain Reaction</topic><topic>Repressor Proteins - physiology</topic><topic>Retina - embryology</topic><topic>Retina - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Shengxiu</creatorcontrib><creatorcontrib>Goldowitz, Dan</creatorcontrib><creatorcontrib>Swanson, Douglas J</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>CrossRef</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>Li, Shengxiu</au><au>Goldowitz, Dan</au><au>Swanson, Douglas J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Requirement of Pax6 for Postnatal Eye Development: Evidence from Experimental Mouse Chimeras</atitle><jtitle>Investigative ophthalmology &amp; visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>48</volume><issue>7</issue><spage>3292</spage><epage>3300</epage><pages>3292-3300</pages><issn>0146-0404</issn><issn>1552-5783</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>The small eye mouse mutant (Sey) is caused by a mutation of the Pax6 gene. Previous studies, in which aggregation chimeras were used, have demonstrated that Sey/Sey cells contribute poorly to the neural retina forming small clumps of cells restricted to the inner retina at embryonic day 16.5. In addition, Sey/+ cells are absent from the lens epithelium during this embryonic period and postnatally. This study was conducted to determine the fates of these Sey/Sey and Sey/+ cells with continued development in chimeric mouse eyes. Observations were made on heterozygous and homozygous Sey cells in chimeric eyes from postnatal day (P)0 to P10. In Sey/Sey&lt;--&gt;wild-type (wt) chimeras, all Sey/Sey cells originating from retinal progenitor cells died at perinatal times. The only remaining Sey/Sey cells in the neural retina were associated with blood vessels, including vascular endothelial cells, pericytes, astrocytes, and microglia, which have extraretinal origins. In contrast, Sey/+ cells formed all retinal cell classes. As previously reported, Sey/Sey cells were absent from the lens and corneal epithelium. However, in contrast to previous reports, Sey/+ cells contributed to the lens epithelium as well as corneal tissues, and Sey/Sey cells were absent from the anterior retinal pigment epithelium. All evidence showed that, when Pax6 is absent at the initial stages of the development, Sey/Sey cells that contribute to the neural retina die, even when wild-type cells are available to provide normal environmental cues.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>17591901</pmid><doi>10.1167/iovs.06-1482</doi><tpages>9</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Chimera - genetics
Chimera - metabolism
Epithelium, Corneal - embryology
Epithelium, Corneal - metabolism
Eye - embryology
Eye - metabolism
Eye and associated structures. Visual pathways and centers. Vision
Eye Proteins - physiology
Female
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Developmental - physiology
Genotype
Homeodomain Proteins - physiology
Immunoenzyme Techniques
Iris - embryology
Iris - metabolism
Lens, Crystalline - embryology
Lens, Crystalline - metabolism
Mice
Mice, Inbred ICR
Microphthalmos - genetics
Microphthalmos - metabolism
Microphthalmos - pathology
Paired Box Transcription Factors - physiology
PAX6 Transcription Factor
Phenotype
Pigment Epithelium of Eye - metabolism
Polymerase Chain Reaction
Repressor Proteins - physiology
Retina - embryology
Retina - metabolism
Vertebrates: nervous system and sense organs
title The Requirement of Pax6 for Postnatal Eye Development: Evidence from Experimental Mouse Chimeras
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