Changes in gene expression and cell shape characterise stages of epibranchial placode‐derived neuron maturation in the chick
Sensory neurons in the head are largely generated from neurogenic placodes. Previous studies have revealed early events in placode development; however, the process of maturation has not been studied. In this study, it has been shown that placodal neurogenesis follows a sequential progression with d...
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Veröffentlicht in: | Journal of anatomy 2015-07, Vol.227 (1), p.89-102 |
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description | Sensory neurons in the head are largely generated from neurogenic placodes. Previous studies have revealed early events in placode development; however, the process of maturation has not been studied. In this study, it has been shown that placodal neurogenesis follows a sequential progression with distinct stages defined by expression of specific markers. These markers highlight domains of maturation within the stream of migratory neuroblasts that extend between the placode and the neural tube. Commitment to neurogenesis occurs in the apical placode, with the newborn neuroblasts delaminating basally and entering a transition zone. The neuroblasts migrate through the transition zone, differentiating further and becoming post‐mitotic as they approach the ganglionic anlage. It has further been demonstrated that this progression from the transition zone to the ganglionic anlage is accompanied by a switch from multipolar to bipolar cell morphology. This sequential progression parallels events observed elsewhere in the nervous system, but here the stages are distinct and anatomically segregated. It is proposed that placodal neurogenesis provides a tractable system to examine the transition between states in neurogenesis. |
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Previous studies have revealed early events in placode development; however, the process of maturation has not been studied. In this study, it has been shown that placodal neurogenesis follows a sequential progression with distinct stages defined by expression of specific markers. These markers highlight domains of maturation within the stream of migratory neuroblasts that extend between the placode and the neural tube. Commitment to neurogenesis occurs in the apical placode, with the newborn neuroblasts delaminating basally and entering a transition zone. The neuroblasts migrate through the transition zone, differentiating further and becoming post‐mitotic as they approach the ganglionic anlage. It has further been demonstrated that this progression from the transition zone to the ganglionic anlage is accompanied by a switch from multipolar to bipolar cell morphology. This sequential progression parallels events observed elsewhere in the nervous system, but here the stages are distinct and anatomically segregated. It is proposed that placodal neurogenesis provides a tractable system to examine the transition between states in neurogenesis.</description><identifier>ISSN: 0021-8782</identifier><identifier>EISSN: 1469-7580</identifier><identifier>DOI: 10.1111/joa.12333</identifier><identifier>PMID: 26076761</identifier><identifier>CODEN: JOANAY</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Animals ; Biomarkers - metabolism ; Cell Differentiation ; Cell Shape - physiology ; chick ; Chick Embryo ; epibranchial ; Gene expression ; Gene Expression - physiology ; Neural Tube - embryology ; Neural Tube - metabolism ; Neurogenesis ; Original ; placode ; sensory ; Sensory Receptor Cells - physiology</subject><ispartof>Journal of anatomy, 2015-07, Vol.227 (1), p.89-102</ispartof><rights>2015 Anatomical Society</rights><rights>2015 Anatomical Society.</rights><rights>Copyright © 2015 Anatomical Society</rights><rights>2015 Anatomical Society 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4763-8c9323f6a90968728fe6e72fcc09e5eb2b833df9d55a0661586147c67c3f99e23</citedby><cites>FETCH-LOGICAL-c4763-8c9323f6a90968728fe6e72fcc09e5eb2b833df9d55a0661586147c67c3f99e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475362/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475362/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26076761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, Alexandra C.</creatorcontrib><creatorcontrib>Fleenor, Stephen J.</creatorcontrib><creatorcontrib>Begbie, Jo</creatorcontrib><title>Changes in gene expression and cell shape characterise stages of epibranchial placode‐derived neuron maturation in the chick</title><title>Journal of anatomy</title><addtitle>J Anat</addtitle><description>Sensory neurons in the head are largely generated from neurogenic placodes. Previous studies have revealed early events in placode development; however, the process of maturation has not been studied. In this study, it has been shown that placodal neurogenesis follows a sequential progression with distinct stages defined by expression of specific markers. These markers highlight domains of maturation within the stream of migratory neuroblasts that extend between the placode and the neural tube. Commitment to neurogenesis occurs in the apical placode, with the newborn neuroblasts delaminating basally and entering a transition zone. The neuroblasts migrate through the transition zone, differentiating further and becoming post‐mitotic as they approach the ganglionic anlage. It has further been demonstrated that this progression from the transition zone to the ganglionic anlage is accompanied by a switch from multipolar to bipolar cell morphology. This sequential progression parallels events observed elsewhere in the nervous system, but here the stages are distinct and anatomically segregated. It is proposed that placodal neurogenesis provides a tractable system to examine the transition between states in neurogenesis.</description><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Cell Differentiation</subject><subject>Cell Shape - physiology</subject><subject>chick</subject><subject>Chick Embryo</subject><subject>epibranchial</subject><subject>Gene expression</subject><subject>Gene Expression - physiology</subject><subject>Neural Tube - embryology</subject><subject>Neural Tube - metabolism</subject><subject>Neurogenesis</subject><subject>Original</subject><subject>placode</subject><subject>sensory</subject><subject>Sensory Receptor Cells - physiology</subject><issn>0021-8782</issn><issn>1469-7580</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks1u1DAQgC0EokvhwAsgS1zgkNY_iX8uSNWKX1XqBc6W15lsvGTtYCctvSAegWfkSXDYUgESEr7Mwd98Y88MQo8pOaHlnO6iPaGMc34HrWgtdCUbRe6iFSGMVkoqdoQe5LwjhHKi6_voiAkihRR0hb6sexu2kLEPeAsBMHweE-TsY8A2tNjBMODc2xGw622yboLkM-A82SUrdhhGv0k2uN7bAY-DdbGF71-_tYW7hBYHmFNx7e00Jzst2lJp6heddx8fonudHTI8uonH6MOrl-_Xb6rzi9dv12fnlaul4JVymjPeCauJFkoy1YEAyTrniIYGNmyjOG873TaNJULQRglaSyek453WwPgxenHwjvNmD62DMCU7mDH5vU3XJlpv_rwJvjfbeGnqWjZcLIJnN4IUP82QJ7P3eWmODRDnbKjQtZaKNOI_UKUFK8MgBX36F7qLcwqlEwuluCCK0UI9P1AuxZwTdLfvpsQsC1CyrPm5AIV98vtHb8lfEy_A6QG48gNc_9tk3l2cHZQ_AD0_vH0</recordid><startdate>201507</startdate><enddate>201507</enddate><creator>Smith, Alexandra C.</creator><creator>Fleenor, Stephen J.</creator><creator>Begbie, Jo</creator><general>Wiley Subscription Services, Inc</general><general>BlackWell Publishing 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>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201507</creationdate><title>Changes in gene expression and cell shape characterise stages of epibranchial placode‐derived neuron maturation in the chick</title><author>Smith, Alexandra C. ; Fleenor, Stephen J. ; Begbie, Jo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4763-8c9323f6a90968728fe6e72fcc09e5eb2b833df9d55a0661586147c67c3f99e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Cell Differentiation</topic><topic>Cell Shape - physiology</topic><topic>chick</topic><topic>Chick Embryo</topic><topic>epibranchial</topic><topic>Gene expression</topic><topic>Gene Expression - physiology</topic><topic>Neural Tube - embryology</topic><topic>Neural Tube - metabolism</topic><topic>Neurogenesis</topic><topic>Original</topic><topic>placode</topic><topic>sensory</topic><topic>Sensory Receptor Cells - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Alexandra C.</creatorcontrib><creatorcontrib>Fleenor, Stephen J.</creatorcontrib><creatorcontrib>Begbie, Jo</creatorcontrib><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>Entomology Abstracts (Full archive)</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of anatomy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Alexandra C.</au><au>Fleenor, Stephen J.</au><au>Begbie, Jo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in gene expression and cell shape characterise stages of epibranchial placode‐derived neuron maturation in the chick</atitle><jtitle>Journal of anatomy</jtitle><addtitle>J Anat</addtitle><date>2015-07</date><risdate>2015</risdate><volume>227</volume><issue>1</issue><spage>89</spage><epage>102</epage><pages>89-102</pages><issn>0021-8782</issn><eissn>1469-7580</eissn><coden>JOANAY</coden><abstract>Sensory neurons in the head are largely generated from neurogenic placodes. Previous studies have revealed early events in placode development; however, the process of maturation has not been studied. In this study, it has been shown that placodal neurogenesis follows a sequential progression with distinct stages defined by expression of specific markers. These markers highlight domains of maturation within the stream of migratory neuroblasts that extend between the placode and the neural tube. Commitment to neurogenesis occurs in the apical placode, with the newborn neuroblasts delaminating basally and entering a transition zone. The neuroblasts migrate through the transition zone, differentiating further and becoming post‐mitotic as they approach the ganglionic anlage. It has further been demonstrated that this progression from the transition zone to the ganglionic anlage is accompanied by a switch from multipolar to bipolar cell morphology. This sequential progression parallels events observed elsewhere in the nervous system, but here the stages are distinct and anatomically segregated. It is proposed that placodal neurogenesis provides a tractable system to examine the transition between states in neurogenesis.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>26076761</pmid><doi>10.1111/joa.12333</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomarkers - metabolism Cell Differentiation Cell Shape - physiology chick Chick Embryo epibranchial Gene expression Gene Expression - physiology Neural Tube - embryology Neural Tube - metabolism Neurogenesis Original placode sensory Sensory Receptor Cells - physiology |
title | Changes in gene expression and cell shape characterise stages of epibranchial placode‐derived neuron maturation in the chick |
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