Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domains
The raphe nuclei represent the origin of central serotonergic projections. The literature distinguishes seven nuclei grouped into rostral and caudal clusters relative to the pons. The boundaries of these nuclei have not been defined precisely enough, particularly with regard to developmental units,...
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creator | Alonso, Antonia Merchán, Paloma Sandoval, Juan E. Sánchez-Arrones, Luisa Garcia-Cazorla, Angels Artuch, Rafael Ferrán, José L. Martínez-de-la-Torre, Margaret Puelles, Luis |
description | The raphe nuclei represent the origin of central serotonergic projections. The literature distinguishes seven nuclei grouped into rostral and caudal clusters relative to the pons. The boundaries of these nuclei have not been defined precisely enough, particularly with regard to developmental units, notably hindbrain rhombomeres. We hold that a developmental point of view considering rhombomeres may explain observed differences in connectivity and function. There are twelve rhombomeres characterized by particular genetic profiles, and each develops between one and four distinct serotonergic populations. We have studied the distribution of the conventional seven raphe nuclei among these twelve units. To this aim, we correlated 5-HT-immunoreacted neurons with rhombomeric boundary landmarks in sagittal mouse brain sections at different developmental stages. Furthermore, we performed a partial genoarchitectonic analysis of the developing raphe nuclei, mapping all known serotonergic differentiation markers, and compared these results, jointly with others found in the literature, with our map of serotonin-containing populations, in order to examine regional variations in correspondence. Examples of regionally selective gene patterns were identified. As a result, we produced a rhombomeric classification of some 45 serotonergic populations, and suggested a corresponding modified terminology. Only a minor rostral part of the dorsal raphe nucleus lies in the midbrain. Some serotonergic neurons were found in rhombomere 4, contrary to the conventional assumption that it lacks such neurons. We expect that our reclassification of raphe nuclei may be useful for causal analysis of their differential molecular specification, as well as for studies of differential connectivity and function. |
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The literature distinguishes seven nuclei grouped into rostral and caudal clusters relative to the pons. The boundaries of these nuclei have not been defined precisely enough, particularly with regard to developmental units, notably hindbrain rhombomeres. We hold that a developmental point of view considering rhombomeres may explain observed differences in connectivity and function. There are twelve rhombomeres characterized by particular genetic profiles, and each develops between one and four distinct serotonergic populations. We have studied the distribution of the conventional seven raphe nuclei among these twelve units. To this aim, we correlated 5-HT-immunoreacted neurons with rhombomeric boundary landmarks in sagittal mouse brain sections at different developmental stages. Furthermore, we performed a partial genoarchitectonic analysis of the developing raphe nuclei, mapping all known serotonergic differentiation markers, and compared these results, jointly with others found in the literature, with our map of serotonin-containing populations, in order to examine regional variations in correspondence. Examples of regionally selective gene patterns were identified. As a result, we produced a rhombomeric classification of some 45 serotonergic populations, and suggested a corresponding modified terminology. Only a minor rostral part of the dorsal raphe nucleus lies in the midbrain. Some serotonergic neurons were found in rhombomere 4, contrary to the conventional assumption that it lacks such neurons. We expect that our reclassification of raphe nuclei may be useful for causal analysis of their differential molecular specification, as well as for studies of differential connectivity and function.</description><identifier>ISSN: 1863-2653</identifier><identifier>EISSN: 1863-2661</identifier><identifier>EISSN: 0340-2061</identifier><identifier>DOI: 10.1007/s00429-012-0456-8</identifier><identifier>PMID: 23052546</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anatomy & physiology ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain ; Cell Biology ; Image Processing, Computer-Assisted ; Immunohistochemistry ; In Situ Hybridization ; Mice ; Neurology ; Neurons ; Neurosciences ; Original ; Original Article ; Raphe Nuclei - cytology ; Raphe Nuclei - growth & development ; Reverse Transcriptase Polymerase Chain Reaction ; Rhombencephalon - cytology ; Rodents ; Serotonergic Neurons - classification ; Serotonergic Neurons - physiology ; Serotonin ; Serotonin - metabolism ; Terminology as Topic</subject><ispartof>Brain Structure and Function, 2013-09, Vol.218 (5), p.1229-1277</ispartof><rights>The Author(s) 2012</rights><rights>Springer-Verlag Berlin Heidelberg 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-77a15f96dcc72329fd77024496f7a176b3d32ada1d4cbacdaac959e932c00cd13</citedby><cites>FETCH-LOGICAL-c551t-77a15f96dcc72329fd77024496f7a176b3d32ada1d4cbacdaac959e932c00cd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00429-012-0456-8$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00429-012-0456-8$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23052546$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alonso, Antonia</creatorcontrib><creatorcontrib>Merchán, Paloma</creatorcontrib><creatorcontrib>Sandoval, Juan E.</creatorcontrib><creatorcontrib>Sánchez-Arrones, Luisa</creatorcontrib><creatorcontrib>Garcia-Cazorla, Angels</creatorcontrib><creatorcontrib>Artuch, Rafael</creatorcontrib><creatorcontrib>Ferrán, José L.</creatorcontrib><creatorcontrib>Martínez-de-la-Torre, Margaret</creatorcontrib><creatorcontrib>Puelles, Luis</creatorcontrib><title>Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domains</title><title>Brain Structure and Function</title><addtitle>Brain Struct Funct</addtitle><addtitle>Brain Struct Funct</addtitle><description>The raphe nuclei represent the origin of central serotonergic projections. The literature distinguishes seven nuclei grouped into rostral and caudal clusters relative to the pons. The boundaries of these nuclei have not been defined precisely enough, particularly with regard to developmental units, notably hindbrain rhombomeres. We hold that a developmental point of view considering rhombomeres may explain observed differences in connectivity and function. There are twelve rhombomeres characterized by particular genetic profiles, and each develops between one and four distinct serotonergic populations. We have studied the distribution of the conventional seven raphe nuclei among these twelve units. To this aim, we correlated 5-HT-immunoreacted neurons with rhombomeric boundary landmarks in sagittal mouse brain sections at different developmental stages. Furthermore, we performed a partial genoarchitectonic analysis of the developing raphe nuclei, mapping all known serotonergic differentiation markers, and compared these results, jointly with others found in the literature, with our map of serotonin-containing populations, in order to examine regional variations in correspondence. Examples of regionally selective gene patterns were identified. As a result, we produced a rhombomeric classification of some 45 serotonergic populations, and suggested a corresponding modified terminology. Only a minor rostral part of the dorsal raphe nucleus lies in the midbrain. Some serotonergic neurons were found in rhombomere 4, contrary to the conventional assumption that it lacks such neurons. We expect that our reclassification of raphe nuclei may be useful for causal analysis of their differential molecular specification, as well as for studies of differential connectivity and function.</description><subject>Anatomy & physiology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Cell Biology</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Mice</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neurosciences</subject><subject>Original</subject><subject>Original Article</subject><subject>Raphe Nuclei - cytology</subject><subject>Raphe Nuclei - growth & development</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Rhombencephalon - cytology</subject><subject>Rodents</subject><subject>Serotonergic Neurons - classification</subject><subject>Serotonergic Neurons - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain Structure and Function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alonso, Antonia</au><au>Merchán, Paloma</au><au>Sandoval, Juan E.</au><au>Sánchez-Arrones, Luisa</au><au>Garcia-Cazorla, Angels</au><au>Artuch, Rafael</au><au>Ferrán, José L.</au><au>Martínez-de-la-Torre, Margaret</au><au>Puelles, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domains</atitle><jtitle>Brain Structure and Function</jtitle><stitle>Brain Struct Funct</stitle><addtitle>Brain Struct Funct</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>218</volume><issue>5</issue><spage>1229</spage><epage>1277</epage><pages>1229-1277</pages><issn>1863-2653</issn><eissn>1863-2661</eissn><eissn>0340-2061</eissn><abstract>The raphe nuclei represent the origin of central serotonergic projections. The literature distinguishes seven nuclei grouped into rostral and caudal clusters relative to the pons. The boundaries of these nuclei have not been defined precisely enough, particularly with regard to developmental units, notably hindbrain rhombomeres. We hold that a developmental point of view considering rhombomeres may explain observed differences in connectivity and function. There are twelve rhombomeres characterized by particular genetic profiles, and each develops between one and four distinct serotonergic populations. We have studied the distribution of the conventional seven raphe nuclei among these twelve units. To this aim, we correlated 5-HT-immunoreacted neurons with rhombomeric boundary landmarks in sagittal mouse brain sections at different developmental stages. Furthermore, we performed a partial genoarchitectonic analysis of the developing raphe nuclei, mapping all known serotonergic differentiation markers, and compared these results, jointly with others found in the literature, with our map of serotonin-containing populations, in order to examine regional variations in correspondence. Examples of regionally selective gene patterns were identified. As a result, we produced a rhombomeric classification of some 45 serotonergic populations, and suggested a corresponding modified terminology. Only a minor rostral part of the dorsal raphe nucleus lies in the midbrain. Some serotonergic neurons were found in rhombomere 4, contrary to the conventional assumption that it lacks such neurons. 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subjects | Anatomy & physiology Animals Biomedical and Life Sciences Biomedicine Brain Cell Biology Image Processing, Computer-Assisted Immunohistochemistry In Situ Hybridization Mice Neurology Neurons Neurosciences Original Original Article Raphe Nuclei - cytology Raphe Nuclei - growth & development Reverse Transcriptase Polymerase Chain Reaction Rhombencephalon - cytology Rodents Serotonergic Neurons - classification Serotonergic Neurons - physiology Serotonin Serotonin - metabolism Terminology as Topic |
title | Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domains |
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