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Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system
Sonic hedgehog (Shh), a morphogen molecule implicated in embryonic tissue patterning, displays inductive, proliferative, neurotrophic and neuroprotective activities on various neural cells. Shh might exert its biological functions through binding to patched (Ptc) associated with smoothened (Smo), le...
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Published in: | The European journal of neuroscience 1999-09, Vol.11 (9), p.3199-3214 |
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description | Sonic hedgehog (Shh), a morphogen molecule implicated in embryonic tissue patterning, displays inductive, proliferative, neurotrophic and neuroprotective activities on various neural cells. Shh might exert its biological functions through binding to patched (Ptc) associated with smoothened (Smo), leading to downstream activation of target genes such as the transcription factor Gli1. We have performed a detailed localization of cells expressing transcripts of Shh, Ptc, Smo and Gli1 in brain and spinal cord of the adult rat as well as in the developing cerebellum. In the adult, Shh‐positive cells were mainly observed in forebrain structures, in the Purkinje cells of the cerebellum and in motor neurons. Ptc‐positive cells were frequently observed in brain areas devoid of any Shh transcripts, except in the median eminence or the facial nucleus, suggesting local Shh signalling. Interestingly, Smo transcripts were predominantly present within circumventricular organs, in granular cells of the dentate gyrus and in neurons of the reticular thalamic nucleus. The presence of Shh, Ptc and Smo transcripts in hypothalamic areas may indicate a role of Shh signalling in the modulation of neuroendocrine functions. The expression pattern of these three genes as well as of Gli1, and their developmental regulation in the cerebellum, suggest a possible role for Hedgehog signalling in the control of various cell populations within the cerebellum, particularly in granule cell proliferation and/or differentiation that might be impaired in proliferative states such as medulloblastomas. |
doi_str_mv | 10.1046/j.1460-9568.1999.00777.x |
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Shh might exert its biological functions through binding to patched (Ptc) associated with smoothened (Smo), leading to downstream activation of target genes such as the transcription factor Gli1. We have performed a detailed localization of cells expressing transcripts of Shh, Ptc, Smo and Gli1 in brain and spinal cord of the adult rat as well as in the developing cerebellum. In the adult, Shh‐positive cells were mainly observed in forebrain structures, in the Purkinje cells of the cerebellum and in motor neurons. Ptc‐positive cells were frequently observed in brain areas devoid of any Shh transcripts, except in the median eminence or the facial nucleus, suggesting local Shh signalling. Interestingly, Smo transcripts were predominantly present within circumventricular organs, in granular cells of the dentate gyrus and in neurons of the reticular thalamic nucleus. The presence of Shh, Ptc and Smo transcripts in hypothalamic areas may indicate a role of Shh signalling in the modulation of neuroendocrine functions. The expression pattern of these three genes as well as of Gli1, and their developmental regulation in the cerebellum, suggest a possible role for Hedgehog signalling in the control of various cell populations within the cerebellum, particularly in granule cell proliferation and/or differentiation that might be impaired in proliferative states such as medulloblastomas.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1046/j.1460-9568.1999.00777.x</identifier><identifier>PMID: 10510184</identifier><identifier>CODEN: EJONEI</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; Blotting, Northern ; Brain cancer ; Brain Chemistry ; Brain Chemistry - physiology ; Brain Mapping ; Brain Neoplasms ; Brain Neoplasms - physiopathology ; Central Nervous System ; Central Nervous System - growth & development ; Central Nervous System - physiology ; Digoxigenin ; Factor IX ; Factor IX - biosynthesis ; Factor IX - genetics ; Gene Expression Regulation ; Gene Expression Regulation - physiology ; Gli1 ; Hedgehog Proteins ; Hybridization ; In Situ Hybridization ; Life Sciences ; Male ; medulloblastomas ; motor neuron ; Mutation ; Nervous system ; Neurons ; Neurons and Cognition ; patched ; Protein Biosynthesis ; Proteins ; Proteins - genetics ; Rats ; Rats, Wistar ; RNA ; RNA - biosynthesis ; RNA - isolation & purification ; RNA Probes ; RNA, Messenger ; RNA, Messenger - biosynthesis ; Signal Transduction ; Signal Transduction - physiology ; smoothened ; Spinal Cord ; Spinal Cord - metabolism ; Trans-Activators ; Transcription factors ; Tumors</subject><ispartof>The European journal of neuroscience, 1999-09, Vol.11 (9), p.3199-3214</ispartof><rights>European Neuroscience Association</rights><rights>Copyright Oxford University Press Sep 1999</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5277-be88c94ea3163489503587f7abfbb1cf00cacde477790290940d8cb09d29b3e13</citedby><cites>FETCH-LOGICAL-c5277-be88c94ea3163489503587f7abfbb1cf00cacde477790290940d8cb09d29b3e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10510184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00173344$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Traiffort, Elisabeth</creatorcontrib><creatorcontrib>Charytoniuk, Dorota</creatorcontrib><creatorcontrib>Watroba, Laurent</creatorcontrib><creatorcontrib>Faure, Hélène</creatorcontrib><creatorcontrib>Sales, Nicole</creatorcontrib><creatorcontrib>Ruat, Martial</creatorcontrib><title>Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Sonic hedgehog (Shh), a morphogen molecule implicated in embryonic tissue patterning, displays inductive, proliferative, neurotrophic and neuroprotective activities on various neural cells. Shh might exert its biological functions through binding to patched (Ptc) associated with smoothened (Smo), leading to downstream activation of target genes such as the transcription factor Gli1. We have performed a detailed localization of cells expressing transcripts of Shh, Ptc, Smo and Gli1 in brain and spinal cord of the adult rat as well as in the developing cerebellum. In the adult, Shh‐positive cells were mainly observed in forebrain structures, in the Purkinje cells of the cerebellum and in motor neurons. Ptc‐positive cells were frequently observed in brain areas devoid of any Shh transcripts, except in the median eminence or the facial nucleus, suggesting local Shh signalling. Interestingly, Smo transcripts were predominantly present within circumventricular organs, in granular cells of the dentate gyrus and in neurons of the reticular thalamic nucleus. The presence of Shh, Ptc and Smo transcripts in hypothalamic areas may indicate a role of Shh signalling in the modulation of neuroendocrine functions. The expression pattern of these three genes as well as of Gli1, and their developmental regulation in the cerebellum, suggest a possible role for Hedgehog signalling in the control of various cell populations within the cerebellum, particularly in granule cell proliferation and/or differentiation that might be impaired in proliferative states such as medulloblastomas.</description><subject>Animals</subject><subject>Blotting, Northern</subject><subject>Brain cancer</subject><subject>Brain Chemistry</subject><subject>Brain Chemistry - physiology</subject><subject>Brain Mapping</subject><subject>Brain Neoplasms</subject><subject>Brain Neoplasms - physiopathology</subject><subject>Central Nervous System</subject><subject>Central Nervous System - growth & development</subject><subject>Central Nervous System - physiology</subject><subject>Digoxigenin</subject><subject>Factor IX</subject><subject>Factor IX - biosynthesis</subject><subject>Factor IX - genetics</subject><subject>Gene Expression Regulation</subject><subject>Gene Expression Regulation - physiology</subject><subject>Gli1</subject><subject>Hedgehog Proteins</subject><subject>Hybridization</subject><subject>In Situ Hybridization</subject><subject>Life Sciences</subject><subject>Male</subject><subject>medulloblastomas</subject><subject>motor neuron</subject><subject>Mutation</subject><subject>Nervous system</subject><subject>Neurons</subject><subject>Neurons and Cognition</subject><subject>patched</subject><subject>Protein Biosynthesis</subject><subject>Proteins</subject><subject>Proteins - genetics</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>RNA</subject><subject>RNA - biosynthesis</subject><subject>RNA - isolation & purification</subject><subject>RNA Probes</subject><subject>RNA, Messenger</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Signal Transduction</subject><subject>Signal Transduction - physiology</subject><subject>smoothened</subject><subject>Spinal Cord</subject><subject>Spinal Cord - metabolism</subject><subject>Trans-Activators</subject><subject>Transcription factors</subject><subject>Tumors</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqNkk-P0zAQxSMEYsvCV0AWB7QcUsaxE9sSl1VZdkFVkfiz5WY5yaRNceISp6Xl0-OQVYU4ACdbnt8beea9KCIUphR49nIzpTyDWKWZnFKl1BRACDE93Ismp8L9aAIqZbGk2Zez6JH3GwCQGU8fRmcUUgpU8km0el37osMeiXWFsfUP09eu9cRVZI3lCtduRXy9ao21dbsihWu2rsW296RuSb9GUuIerdsORdOWxJQ725PO9KTFbu92nvij77F5HD2ojPX45O48jz6_ufo0u4nn76_fzi7ncZEmQsQ5SlkojobRjHGpUmCpFJUweZXntKgAClOUyMO0ChIFikMpixxUmaicIWXn0Yux79pYve3qxnRH7Uytby7nengDoIIxzvcD-3xkt537tkPf6yYsA601LYafawFCUk7VP8GACJokIoAXfwclSEF5mrCAPvsD3bhdF_bsdQI8EVnGZYDkCBWd877D6jQSBT0kQW_0YLgeDNdDEvSvJOhDkD6967_LGyx_E47WB-DVCHyvLR7_u7G-ercIlyCPR3kd7D2c5Kb7qjPBRKqXi2s9Ex-Xy9vFB33LfgIl2NCf</recordid><startdate>199909</startdate><enddate>199909</enddate><creator>Traiffort, Elisabeth</creator><creator>Charytoniuk, Dorota</creator><creator>Watroba, Laurent</creator><creator>Faure, Hélène</creator><creator>Sales, Nicole</creator><creator>Ruat, Martial</creator><general>Blackwell Science Ltd</general><general>Wiley Subscription Services, Inc</general><general>Wiley</general><scope>BSCLL</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>199909</creationdate><title>Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system</title><author>Traiffort, Elisabeth ; Charytoniuk, Dorota ; Watroba, Laurent ; Faure, Hélène ; Sales, Nicole ; Ruat, Martial</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5277-be88c94ea3163489503587f7abfbb1cf00cacde477790290940d8cb09d29b3e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Blotting, Northern</topic><topic>Brain cancer</topic><topic>Brain Chemistry</topic><topic>Brain Chemistry - physiology</topic><topic>Brain Mapping</topic><topic>Brain Neoplasms</topic><topic>Brain Neoplasms - physiopathology</topic><topic>Central Nervous System</topic><topic>Central Nervous System - growth & development</topic><topic>Central Nervous System - physiology</topic><topic>Digoxigenin</topic><topic>Factor IX</topic><topic>Factor IX - biosynthesis</topic><topic>Factor IX - genetics</topic><topic>Gene Expression Regulation</topic><topic>Gene Expression Regulation - physiology</topic><topic>Gli1</topic><topic>Hedgehog Proteins</topic><topic>Hybridization</topic><topic>In Situ Hybridization</topic><topic>Life Sciences</topic><topic>Male</topic><topic>medulloblastomas</topic><topic>motor neuron</topic><topic>Mutation</topic><topic>Nervous system</topic><topic>Neurons</topic><topic>Neurons and Cognition</topic><topic>patched</topic><topic>Protein Biosynthesis</topic><topic>Proteins</topic><topic>Proteins - genetics</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>RNA</topic><topic>RNA - biosynthesis</topic><topic>RNA - isolation & purification</topic><topic>RNA Probes</topic><topic>RNA, Messenger</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Signal Transduction</topic><topic>Signal Transduction - physiology</topic><topic>smoothened</topic><topic>Spinal Cord</topic><topic>Spinal Cord - metabolism</topic><topic>Trans-Activators</topic><topic>Transcription factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Traiffort, Elisabeth</creatorcontrib><creatorcontrib>Charytoniuk, Dorota</creatorcontrib><creatorcontrib>Watroba, Laurent</creatorcontrib><creatorcontrib>Faure, Hélène</creatorcontrib><creatorcontrib>Sales, Nicole</creatorcontrib><creatorcontrib>Ruat, Martial</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Traiffort, Elisabeth</au><au>Charytoniuk, Dorota</au><au>Watroba, Laurent</au><au>Faure, Hélène</au><au>Sales, Nicole</au><au>Ruat, Martial</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>1999-09</date><risdate>1999</risdate><volume>11</volume><issue>9</issue><spage>3199</spage><epage>3214</epage><pages>3199-3214</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><coden>EJONEI</coden><abstract>Sonic hedgehog (Shh), a morphogen molecule implicated in embryonic tissue patterning, displays inductive, proliferative, neurotrophic and neuroprotective activities on various neural cells. Shh might exert its biological functions through binding to patched (Ptc) associated with smoothened (Smo), leading to downstream activation of target genes such as the transcription factor Gli1. We have performed a detailed localization of cells expressing transcripts of Shh, Ptc, Smo and Gli1 in brain and spinal cord of the adult rat as well as in the developing cerebellum. In the adult, Shh‐positive cells were mainly observed in forebrain structures, in the Purkinje cells of the cerebellum and in motor neurons. Ptc‐positive cells were frequently observed in brain areas devoid of any Shh transcripts, except in the median eminence or the facial nucleus, suggesting local Shh signalling. Interestingly, Smo transcripts were predominantly present within circumventricular organs, in granular cells of the dentate gyrus and in neurons of the reticular thalamic nucleus. The presence of Shh, Ptc and Smo transcripts in hypothalamic areas may indicate a role of Shh signalling in the modulation of neuroendocrine functions. The expression pattern of these three genes as well as of Gli1, and their developmental regulation in the cerebellum, suggest a possible role for Hedgehog signalling in the control of various cell populations within the cerebellum, particularly in granule cell proliferation and/or differentiation that might be impaired in proliferative states such as medulloblastomas.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>10510184</pmid><doi>10.1046/j.1460-9568.1999.00777.x</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Blotting, Northern Brain cancer Brain Chemistry Brain Chemistry - physiology Brain Mapping Brain Neoplasms Brain Neoplasms - physiopathology Central Nervous System Central Nervous System - growth & development Central Nervous System - physiology Digoxigenin Factor IX Factor IX - biosynthesis Factor IX - genetics Gene Expression Regulation Gene Expression Regulation - physiology Gli1 Hedgehog Proteins Hybridization In Situ Hybridization Life Sciences Male medulloblastomas motor neuron Mutation Nervous system Neurons Neurons and Cognition patched Protein Biosynthesis Proteins Proteins - genetics Rats Rats, Wistar RNA RNA - biosynthesis RNA - isolation & purification RNA Probes RNA, Messenger RNA, Messenger - biosynthesis Signal Transduction Signal Transduction - physiology smoothened Spinal Cord Spinal Cord - metabolism Trans-Activators Transcription factors Tumors |
title | Discrete localizations of hedgehog signalling components in the developing and adult rat nervous system |
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