A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway
The fish optic nerve regeneration process takes more than 100 days after axotomy and comprises four stages: neurite sprouting (1–4 days), axonal elongation (5–30 days), synaptic refinement (35–80 days) and functional recovery (100–120 days). We screened genes specifically upregulated in each stage f...
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description | The fish optic nerve regeneration process takes more than 100 days after axotomy and comprises four stages: neurite sprouting (1–4 days), axonal elongation (5–30 days), synaptic refinement (35–80 days) and functional recovery (100–120 days). We screened genes specifically upregulated in each stage from axotomized fish retina. The mRNAs for heat shock protein 70 and insulin-like growth factor-1 rapidly increased in the retinal ganglion cells soon after axotomy and function as cell-survival factors. Purpurin mRNA rapidly and transiently increased in the photoreceptors and purpurin protein diffusely increased in all nuclear layers at 1–4 days after injury. The purpurin gene has an active retinol-binding site and a signal peptide. Purpurin with retinol functions as a sprouting factor for thin neurites. This neurite-sprouting effect was closely mimicked by retinoic acid and blocked by its inhibitor. We propose that purpurin works as a retinol transporter to supply retinoic acid to damaged RGCs which in turn activates target genes. We also searched for genes involved in the second stage of regeneration. The mRNA of retinoid-signaling molecules increased in retinal ganglion cells at 7–14 days after injury and tissue transglutaminase and neuronal nitric oxide synthase mRNAs, RA-target genes, increased in retinal ganglion cells at 10–30 days after injury. They function as factors for the outgrowth of thick, long neurites. Here we present a retinoid-signaling hypothesis to explain molecular events during the early stages of optic nerve regeneration in fish.
•Many genes are involved in the fish optic nerve regeneration processes.•A retinol-binding protein, purpurin was induced in the retina during the early stage.•Retinoic acid (RA) signaling molecules were then increased in the damaged retina.•RA-target genes such as tissue TG and nNOS were induced thereafter in the retina.•The RA signaling pathway can explain the early stage of regeneration process. |
doi_str_mv | 10.1016/j.preteyeres.2013.07.004 |
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•Many genes are involved in the fish optic nerve regeneration processes.•A retinol-binding protein, purpurin was induced in the retina during the early stage.•Retinoic acid (RA) signaling molecules were then increased in the damaged retina.•RA-target genes such as tissue TG and nNOS were induced thereafter in the retina.•The RA signaling pathway can explain the early stage of regeneration process.</description><identifier>ISSN: 1350-9462</identifier><identifier>EISSN: 1873-1635</identifier><identifier>DOI: 10.1016/j.preteyeres.2013.07.004</identifier><identifier>PMID: 23994437</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Anthraquinones - metabolism ; Axon sprouting ; Factor XIII - metabolism ; Fish retina ; Fishes - physiology ; HSP70 Heat-Shock Proteins - metabolism ; Nerve Regeneration - genetics ; Nerve Regeneration - physiology ; Nitric Oxide Synthase Type I - metabolism ; NO signaling ; Optic Nerve - metabolism ; Optic Nerve - physiopathology ; Optic Nerve Injuries - metabolism ; Optic Nerve Injuries - physiopathology ; Optic nerve regeneration ; Purpurin ; Receptors, Retinoic Acid - genetics ; Retinal Ganglion Cells - cytology ; Retinal Ganglion Cells - metabolism ; Retinoid signaling ; RNA, Messenger - metabolism ; Signal Transduction - physiology ; Somatomedins - metabolism</subject><ispartof>Progress in retinal and eye research, 2013-11, Vol.37, p.13-30</ispartof><rights>2013 Elsevier Ltd</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-5389d9f824793fb3db33e598e9af4ee3c1efd1c0b90ac86df6ddf797d21ce8903</citedby><cites>FETCH-LOGICAL-c473t-5389d9f824793fb3db33e598e9af4ee3c1efd1c0b90ac86df6ddf797d21ce8903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.preteyeres.2013.07.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23994437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato, Satoru</creatorcontrib><creatorcontrib>Matsukawa, Toru</creatorcontrib><creatorcontrib>Koriyama, Yoshiki</creatorcontrib><creatorcontrib>Sugitani, Kayo</creatorcontrib><creatorcontrib>Ogai, Kazuhiro</creatorcontrib><title>A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway</title><title>Progress in retinal and eye research</title><addtitle>Prog Retin Eye Res</addtitle><description>The fish optic nerve regeneration process takes more than 100 days after axotomy and comprises four stages: neurite sprouting (1–4 days), axonal elongation (5–30 days), synaptic refinement (35–80 days) and functional recovery (100–120 days). We screened genes specifically upregulated in each stage from axotomized fish retina. The mRNAs for heat shock protein 70 and insulin-like growth factor-1 rapidly increased in the retinal ganglion cells soon after axotomy and function as cell-survival factors. Purpurin mRNA rapidly and transiently increased in the photoreceptors and purpurin protein diffusely increased in all nuclear layers at 1–4 days after injury. The purpurin gene has an active retinol-binding site and a signal peptide. Purpurin with retinol functions as a sprouting factor for thin neurites. This neurite-sprouting effect was closely mimicked by retinoic acid and blocked by its inhibitor. We propose that purpurin works as a retinol transporter to supply retinoic acid to damaged RGCs which in turn activates target genes. We also searched for genes involved in the second stage of regeneration. The mRNA of retinoid-signaling molecules increased in retinal ganglion cells at 7–14 days after injury and tissue transglutaminase and neuronal nitric oxide synthase mRNAs, RA-target genes, increased in retinal ganglion cells at 10–30 days after injury. They function as factors for the outgrowth of thick, long neurites. Here we present a retinoid-signaling hypothesis to explain molecular events during the early stages of optic nerve regeneration in fish.
•Many genes are involved in the fish optic nerve regeneration processes.•A retinol-binding protein, purpurin was induced in the retina during the early stage.•Retinoic acid (RA) signaling molecules were then increased in the damaged retina.•RA-target genes such as tissue TG and nNOS were induced thereafter in the retina.•The RA signaling pathway can explain the early stage of regeneration process.</description><subject>Animals</subject><subject>Anthraquinones - metabolism</subject><subject>Axon sprouting</subject><subject>Factor XIII - metabolism</subject><subject>Fish retina</subject><subject>Fishes - physiology</subject><subject>HSP70 Heat-Shock Proteins - metabolism</subject><subject>Nerve Regeneration - genetics</subject><subject>Nerve Regeneration - physiology</subject><subject>Nitric Oxide Synthase Type I - metabolism</subject><subject>NO signaling</subject><subject>Optic Nerve - metabolism</subject><subject>Optic Nerve - physiopathology</subject><subject>Optic Nerve Injuries - metabolism</subject><subject>Optic Nerve Injuries - physiopathology</subject><subject>Optic nerve regeneration</subject><subject>Purpurin</subject><subject>Receptors, Retinoic Acid - genetics</subject><subject>Retinal Ganglion Cells - cytology</subject><subject>Retinal Ganglion Cells - metabolism</subject><subject>Retinoid signaling</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction - physiology</subject><subject>Somatomedins - metabolism</subject><issn>1350-9462</issn><issn>1873-1635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS1URP_AV0A-ckk6jpPY7q2toEWq1Es5cLK89njXq8QOdrZovz1ZbaFHeponze_NSO8RQhnUDFh_ua2njDPuMWOpG2C8BlEDtO_IGZOCV6zn3cmieQeVavvmlJyXsgWAHlT3gZw2XKm25eKM_LymYxrQ7gaT6Yh2Y2IoI02epmkOlkbMz0gzrnFRZg4p0hCpD2VzRZ82h80cYgqOlrCOZghxTSczb36b_Ufy3puh4KeXeUF-fPv6dHtfPTzefb-9fqhsK_hcdVwqp7xsWqG4X3G34hw7JVEZ3yJyy9A7ZmGlwFjZO98754USrmEWpQJ-Qb4c7045_dphmfUYisVhMBHTrmjWAQgJb0LbTjLZqK5fUHlEbU6lZPR6ymE0ea8Z6EMHeqtfO9CHDjQIvXSwWD-_fNmtRnT_jH9DX4CbI4BLLM8Bsy42YLToQkY7a5fC_7_8AROmnqA</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Kato, Satoru</creator><creator>Matsukawa, Toru</creator><creator>Koriyama, Yoshiki</creator><creator>Sugitani, Kayo</creator><creator>Ogai, Kazuhiro</creator><general>Elsevier Ltd</general><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><scope>7TK</scope></search><sort><creationdate>201311</creationdate><title>A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway</title><author>Kato, Satoru ; Matsukawa, Toru ; Koriyama, Yoshiki ; Sugitani, Kayo ; Ogai, Kazuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-5389d9f824793fb3db33e598e9af4ee3c1efd1c0b90ac86df6ddf797d21ce8903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anthraquinones - metabolism</topic><topic>Axon sprouting</topic><topic>Factor XIII - metabolism</topic><topic>Fish retina</topic><topic>Fishes - physiology</topic><topic>HSP70 Heat-Shock Proteins - metabolism</topic><topic>Nerve Regeneration - genetics</topic><topic>Nerve Regeneration - physiology</topic><topic>Nitric Oxide Synthase Type I - metabolism</topic><topic>NO signaling</topic><topic>Optic Nerve - metabolism</topic><topic>Optic Nerve - physiopathology</topic><topic>Optic Nerve Injuries - metabolism</topic><topic>Optic Nerve Injuries - physiopathology</topic><topic>Optic nerve regeneration</topic><topic>Purpurin</topic><topic>Receptors, Retinoic Acid - genetics</topic><topic>Retinal Ganglion Cells - cytology</topic><topic>Retinal Ganglion Cells - metabolism</topic><topic>Retinoid signaling</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction - physiology</topic><topic>Somatomedins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato, Satoru</creatorcontrib><creatorcontrib>Matsukawa, Toru</creatorcontrib><creatorcontrib>Koriyama, Yoshiki</creatorcontrib><creatorcontrib>Sugitani, Kayo</creatorcontrib><creatorcontrib>Ogai, Kazuhiro</creatorcontrib><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><collection>Neurosciences Abstracts</collection><jtitle>Progress in retinal and eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato, Satoru</au><au>Matsukawa, Toru</au><au>Koriyama, Yoshiki</au><au>Sugitani, Kayo</au><au>Ogai, Kazuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway</atitle><jtitle>Progress in retinal and eye research</jtitle><addtitle>Prog Retin Eye Res</addtitle><date>2013-11</date><risdate>2013</risdate><volume>37</volume><spage>13</spage><epage>30</epage><pages>13-30</pages><issn>1350-9462</issn><eissn>1873-1635</eissn><abstract>The fish optic nerve regeneration process takes more than 100 days after axotomy and comprises four stages: neurite sprouting (1–4 days), axonal elongation (5–30 days), synaptic refinement (35–80 days) and functional recovery (100–120 days). We screened genes specifically upregulated in each stage from axotomized fish retina. The mRNAs for heat shock protein 70 and insulin-like growth factor-1 rapidly increased in the retinal ganglion cells soon after axotomy and function as cell-survival factors. Purpurin mRNA rapidly and transiently increased in the photoreceptors and purpurin protein diffusely increased in all nuclear layers at 1–4 days after injury. The purpurin gene has an active retinol-binding site and a signal peptide. Purpurin with retinol functions as a sprouting factor for thin neurites. This neurite-sprouting effect was closely mimicked by retinoic acid and blocked by its inhibitor. We propose that purpurin works as a retinol transporter to supply retinoic acid to damaged RGCs which in turn activates target genes. We also searched for genes involved in the second stage of regeneration. The mRNA of retinoid-signaling molecules increased in retinal ganglion cells at 7–14 days after injury and tissue transglutaminase and neuronal nitric oxide synthase mRNAs, RA-target genes, increased in retinal ganglion cells at 10–30 days after injury. They function as factors for the outgrowth of thick, long neurites. Here we present a retinoid-signaling hypothesis to explain molecular events during the early stages of optic nerve regeneration in fish.
•Many genes are involved in the fish optic nerve regeneration processes.•A retinol-binding protein, purpurin was induced in the retina during the early stage.•Retinoic acid (RA) signaling molecules were then increased in the damaged retina.•RA-target genes such as tissue TG and nNOS were induced thereafter in the retina.•The RA signaling pathway can explain the early stage of regeneration process.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>23994437</pmid><doi>10.1016/j.preteyeres.2013.07.004</doi><tpages>18</tpages></addata></record> |
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subjects | Animals Anthraquinones - metabolism Axon sprouting Factor XIII - metabolism Fish retina Fishes - physiology HSP70 Heat-Shock Proteins - metabolism Nerve Regeneration - genetics Nerve Regeneration - physiology Nitric Oxide Synthase Type I - metabolism NO signaling Optic Nerve - metabolism Optic Nerve - physiopathology Optic Nerve Injuries - metabolism Optic Nerve Injuries - physiopathology Optic nerve regeneration Purpurin Receptors, Retinoic Acid - genetics Retinal Ganglion Cells - cytology Retinal Ganglion Cells - metabolism Retinoid signaling RNA, Messenger - metabolism Signal Transduction - physiology Somatomedins - metabolism |
title | A molecular mechanism of optic nerve regeneration in fish: The retinoid signaling pathway |
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