Eye development and retinal differentiation in an altricial fish species, the senegalese sole (Solea senegalensis, Kaup 1858)
Identifieur interne : 001288 ( Istex/Corpus ); précédent : 001287; suivant : 001289Eye development and retinal differentiation in an altricial fish species, the senegalese sole (Solea senegalensis, Kaup 1858)
Auteurs : Ruth Bejarano-Escobar ; Manuel Blasco ; Willem J. Degrip ; José Antonio Oyola-Velasco ; Gervasio Martín-Partido ; Javier Francisco-MorcilloSource :
- Journal of Experimental Zoology Part B: Molecular and Developmental Evolution [ 1552-5007 ] ; 2010-11-15.
Abstract
We describe the major events in the retinogenesis in an altricial fish species, the Senegalese sole. The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. J. Exp. Zool. (Mol. Dev. Evol.) 314B:580–605, 2010. © 2010 Wiley‐Liss, Inc.
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DOI: 10.1002/jez.b.21363
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The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. J. Exp. Zool. (Mol. Dev. 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The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. J. Exp. Zool. (Mol. Dev. 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The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. J. Exp. Zool. (Mol. Dev. 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type="pageFirst">580</numbering><numbering type="pageLast">605</numbering></numberingGroup><correspondenceTo>Departamento de Biología Celular, Facultad de Veterinaria, Universidad de Extremadura, Avda. de la Universidad s/n, 10003, Cáceres, Spain===</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:JEZ.JEZ21363.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="10"></count><count type="tableTotal" number="2"></count><count type="referenceTotal" number="126"></count></countGroup><titleGroup><title type="main" xml:lang="en">Eye development and retinal differentiation in an altricial fish species, the senegalese sole (<i>Solea senegalensis</i>, Kaup 1858)</title><title type="short" xml:lang="en">RETINOGENESIS IN <fi>Solea senegalensis</fi></title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Ruth</givenNames><familyName>Bejarano‐Escobar</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Manuel</givenNames><familyName>Blasco</familyName></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Willem J.</givenNames><familyName>DeGrip</familyName></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af4"><personName><givenNames>José Antonio</givenNames><familyName>Oyola‐Velasco</familyName></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Gervasio</givenNames><familyName>Martín‐Partido</familyName></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af1 #af5" corresponding="yes"><personName><givenNames>Javier</givenNames><familyName>Francisco‐Morcillo</familyName></personName><contactDetails><email>morcillo@unex.es</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="ES" type="organization"><unparsedAffiliation>Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="ES" type="organization"><unparsedAffiliation>Acuitenco Spin‐Off, Universidad de Extremadura, Badajoz, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="NL" type="organization"><unparsedAffiliation>Department of Biochemistry, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="ES" type="organization"><unparsedAffiliation>Departamento de Matemáticas, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="ES" type="organization"><unparsedAffiliation>Departamento de Biología Celular, Facultad de Veterinaria, Universidad de Extremadura, Cáceres, Spain</unparsedAffiliation></affiliation></affiliationGroup><fundingInfo><fundingAgency>Spanish Ministerio de Ciencia y Tecnología</fundingAgency><fundingNumber>BFU2007‐67540</fundingNumber></fundingInfo><fundingInfo><fundingAgency>Junta de Extremadura</fundingAgency><fundingNumber>PRI06A195</fundingNumber></fundingInfo><abstractGroup><abstract type="main" xml:lang="de"><title type="main">Abstract</title><p>We describe the major events in the retinogenesis in an altricial fish species, the Senegalese sole. The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. <i>J. Exp. Zool. (Mol. Dev. Evol.) 314B:580–605, 2010</i>. © 2010 Wiley‐Liss, Inc.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Eye development and retinal differentiation in an altricial fish species, the senegalese sole (Solea senegalensis, Kaup 1858)</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>RETINOGENESIS IN Solea senegalensis</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Eye development and retinal differentiation in an altricial fish species, the senegalese sole (Solea senegalensis, Kaup 1858)</title></titleInfo><name type="personal"><namePart type="given">Ruth</namePart><namePart type="family">Bejarano‐Escobar</namePart><affiliation>Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Manuel</namePart><namePart type="family">Blasco</namePart><affiliation>Acuitenco Spin‐Off, Universidad de Extremadura, Badajoz, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Willem J.</namePart><namePart type="family">DeGrip</namePart><affiliation>Department of Biochemistry, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">José Antonio</namePart><namePart type="family">Oyola‐Velasco</namePart><affiliation>Departamento de Matemáticas, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Gervasio</namePart><namePart type="family">Martín‐Partido</namePart><affiliation>Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Javier</namePart><namePart type="family">Francisco‐Morcillo</namePart><affiliation>Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain</affiliation><affiliation>Departamento de Biología Celular, Facultad de Veterinaria, Universidad de Extremadura, Cáceres, Spain</affiliation><affiliation>Departamento de Biología Celular, Facultad de Veterinaria, Universidad de Extremadura, Avda. de la Universidad s/n, 10003, Cáceres, Spain===</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2010-11-15</dateIssued><dateCaptured encoding="w3cdtf">2010-02-12</dateCaptured><dateValid encoding="w3cdtf">2010-05-17</dateValid><copyrightDate encoding="w3cdtf">2010</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">10</extent><extent unit="tables">2</extent><extent unit="references">126</extent></physicalDescription><abstract lang="de">We describe the major events in the retinogenesis in an altricial fish species, the Senegalese sole. The major developmental events in the sole retina occurred early after hatching (posthatching day 0, P0). Thus, (1) plexiform layers became recognizable at P1. (2) Proliferative activity disappeared from the central retina at P1, and, as development progressed, became restricted to cells located in the circumferential germinal zone, and to sparse cells dispersed throughout the inner nuclear layer and the outer nuclear layer. (3) Apoptotic cells were sparsely observed, randomly localized in all three nuclear layers of the early posthatching retina from P0 to P4. (4) The first synaptic vesicles were detected at P0 in early postmitotic ganglion cells. However, their appearance in the plexiform layers was delayed until P2. (5) The neurochemical development of most major retinal cell classes occurred between P0 and P5. Thus, although Isl1 immunoreactive ganglion cells were the first to become postmitotic in the vitreal surface of the central retina at P0, the first glutamine synthetase‐expressing Müller cells appeared in the central retina by P5. The onset of expression for other retinal markers, such as rod opsin, calretinin, parvalbumin, α‐tyrosine hydroxylase, and α‐protein kinase C, occurred between P2 and P4. Our results suggest that the most relevant processes involved in Senegalese sole retinogenesis occur during the prolarval and early larval stages (P0–P5). Furthermore, we conclude that altricial fish species may constitute a convenient model organism to address the relationship between the structural and functional development of sensory organs with the acquisition of behavioral repertoires. J. Exp. Zool. (Mol. Dev. Evol.) 314B:580–605, 2010. © 2010 Wiley‐Liss, Inc.</abstract><note type="funding">Spanish Ministerio de Ciencia y Tecnología - No. BFU2007‐67540; </note><note type="funding">Junta de Extremadura - No. PRI06A195; </note><relatedItem type="host"><titleInfo><title>Journal of Experimental Zoology Part B: Molecular and Developmental Evolution</title></titleInfo><titleInfo type="abbreviated"><title>J. Exp. Zool.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Research Article</topic></subject><identifier type="ISSN">1552-5007</identifier><identifier type="eISSN">1552-5015</identifier><identifier type="DOI">10.1002/(ISSN)1552-5015</identifier><identifier type="PublisherID">JEZ</identifier><part><date>2010</date><detail type="volume"><caption>vol.</caption><number>314B</number></detail><detail type="issue"><caption>no.</caption><number>7</number></detail><extent unit="pages"><start>580</start><end>605</end><total>26</total></extent></part></relatedItem><relatedItem type="preceding"><titleInfo><title>Journal of Experimental Zoology</title></titleInfo><identifier type="ISSN">0022-104X</identifier><identifier type="ISSN">1097-010X</identifier><part><date point="end">2004</date></part></relatedItem><identifier type="istex">10F78AFBE9E73C2A353DB76052156D40311A4E7D</identifier><identifier type="DOI">10.1002/jez.b.21363</identifier><identifier type="ArticleID">JEZ21363</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2010 Wiley‐Liss, Inc., A Wiley Company</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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