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Distribution of Gonadotropin-Releasing Hormone Neurones in the Chick Forebrain is Independent of Lineage Relationships Among Cells of the Early Nasal Placode
The regulation of reproduction depends upon the successful migration of gonadotropin‐releasing hormone (GnRH) neurones from the nasal placode to the ventral forebrain during embryogenesis. Within the central nervous system (CNS), these neurones migrate to stereotyped, highly reproducible locations i...
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Published in: | Journal of neuroendocrinology 2002-03, Vol.14 (3), p.207-212 |
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creator | Silverman, A.-J. Cserjesi, P. Kanter, E. |
description | The regulation of reproduction depends upon the successful migration of gonadotropin‐releasing hormone (GnRH) neurones from the nasal placode to the ventral forebrain during embryogenesis. Within the central nervous system (CNS), these neurones migrate to stereotyped, highly reproducible locations in septal, preoptic and hypothalamic nuclei. We postulated that lineage relationships (descent from a common precursor) might predict the final location of these neurones. To test this hypothesis, a complex retroviral library was used to label dividing cells in the placode and subsequently to identify them by the presence of the alkaline phosphatase marker. GnRH was detected immunocytochemically and lineage relationships determined by single cell polymerase chain reaction and sequencing of the degenerate oligonucleotide component of the retrovirus. GnRH‐positive and GnRH‐negative neurones were confined to the side ipsilateral to the injection; many cells derived from the placode that entered the CNS did not contain GnRH. This precise method of identifying and mapping the progeny of single neurones revealed that GnRH cells in any given area were derived from multiple precursors. This developmental pattern may contribute to assuring that all CNS locations critical to the orchestration of reproductive events will be populated by GnRH neurones. |
doi_str_mv | 10.1046/j.0007-1331.2001.00762.x |
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Within the central nervous system (CNS), these neurones migrate to stereotyped, highly reproducible locations in septal, preoptic and hypothalamic nuclei. We postulated that lineage relationships (descent from a common precursor) might predict the final location of these neurones. To test this hypothesis, a complex retroviral library was used to label dividing cells in the placode and subsequently to identify them by the presence of the alkaline phosphatase marker. GnRH was detected immunocytochemically and lineage relationships determined by single cell polymerase chain reaction and sequencing of the degenerate oligonucleotide component of the retrovirus. GnRH‐positive and GnRH‐negative neurones were confined to the side ipsilateral to the injection; many cells derived from the placode that entered the CNS did not contain GnRH. This precise method of identifying and mapping the progeny of single neurones revealed that GnRH cells in any given area were derived from multiple precursors. This developmental pattern may contribute to assuring that all CNS locations critical to the orchestration of reproductive events will be populated by GnRH neurones.</description><identifier>ISSN: 0953-8194</identifier><identifier>EISSN: 1365-2826</identifier><identifier>DOI: 10.1046/j.0007-1331.2001.00762.x</identifier><identifier>PMID: 11999720</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science, Ltd</publisher><subject>Animals ; Cell Line ; Chick Embryo - cytology ; Chick Embryo - metabolism ; Gonadotropin-Releasing Hormone - metabolism ; LHRH ; neuronal migration ; Neurons - cytology ; Neurons - metabolism ; Prosencephalon - embryology ; reproduction ; Respiratory System - embryology ; retrovirus ; Tissue Distribution</subject><ispartof>Journal of neuroendocrinology, 2002-03, Vol.14 (3), p.207-212</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4682-6af1e8d5058068213d7def312397dddc0296f45691c69daddf683fb17acaa60a3</citedby><cites>FETCH-LOGICAL-c4682-6af1e8d5058068213d7def312397dddc0296f45691c69daddf683fb17acaa60a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11999720$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silverman, A.-J.</creatorcontrib><creatorcontrib>Cserjesi, P.</creatorcontrib><creatorcontrib>Kanter, E.</creatorcontrib><title>Distribution of Gonadotropin-Releasing Hormone Neurones in the Chick Forebrain is Independent of Lineage Relationships Among Cells of the Early Nasal Placode</title><title>Journal of neuroendocrinology</title><addtitle>J Neuroendocrinol</addtitle><description>The regulation of reproduction depends upon the successful migration of gonadotropin‐releasing hormone (GnRH) neurones from the nasal placode to the ventral forebrain during embryogenesis. Within the central nervous system (CNS), these neurones migrate to stereotyped, highly reproducible locations in septal, preoptic and hypothalamic nuclei. We postulated that lineage relationships (descent from a common precursor) might predict the final location of these neurones. To test this hypothesis, a complex retroviral library was used to label dividing cells in the placode and subsequently to identify them by the presence of the alkaline phosphatase marker. GnRH was detected immunocytochemically and lineage relationships determined by single cell polymerase chain reaction and sequencing of the degenerate oligonucleotide component of the retrovirus. GnRH‐positive and GnRH‐negative neurones were confined to the side ipsilateral to the injection; many cells derived from the placode that entered the CNS did not contain GnRH. This precise method of identifying and mapping the progeny of single neurones revealed that GnRH cells in any given area were derived from multiple precursors. This developmental pattern may contribute to assuring that all CNS locations critical to the orchestration of reproductive events will be populated by GnRH neurones.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Chick Embryo - cytology</subject><subject>Chick Embryo - metabolism</subject><subject>Gonadotropin-Releasing Hormone - metabolism</subject><subject>LHRH</subject><subject>neuronal migration</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Prosencephalon - embryology</subject><subject>reproduction</subject><subject>Respiratory System - embryology</subject><subject>retrovirus</subject><subject>Tissue Distribution</subject><issn>0953-8194</issn><issn>1365-2826</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqNkdFq2zAUhsXYWNNurzB0tTunkmVLNuympEnaEtxSOnYpFOs4UepInmSz5GH2rpOX0N0OhM454v__I_gQwpRMKcn49W5KCBEJZYxOU0JoHAVPp4d3aEIZz5O0SPl7NCFlzpKCltkFugxhF4UiZ-QjuqC0LEuRkgn6fWtC78166I2z2DV46azSrveuMzZ5hhZUMHaD75zfOwu4gsHHGrCxuN8Cnm1N_YoXzsPaq_hmAr63GjqIl-3HwJWxoDaAY5Yal4St6QK-iWkbPIO2DaNojJor3x5xpYJq8VOraqfhE_rQqDbA53O9Qt8X85fZXbJ6XN7PblZJnfEiTbhqKBQ6J3lB4kyZFhoaRlNWCq11TdKSN1nOS1rzUiutG16wZk2FqpXiRLEr9PWU23n3c4DQy70JdfycsuCGIAXl8WR5FBYnYe1dCB4a2XmzV_4oKZEjGrmTIxo5opEjGvkXjTxE65fzjmG9B_3PeGYRBd9Ogl-mheN_B8uHah6baE9O9ggUDm925V8lF0zk8ke1lIvnrErzl0zesj9Ilq4u</recordid><startdate>200203</startdate><enddate>200203</enddate><creator>Silverman, A.-J.</creator><creator>Cserjesi, P.</creator><creator>Kanter, E.</creator><general>Blackwell Science, Ltd</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>7X8</scope></search><sort><creationdate>200203</creationdate><title>Distribution of Gonadotropin-Releasing Hormone Neurones in the Chick Forebrain is Independent of Lineage Relationships Among Cells of the Early Nasal Placode</title><author>Silverman, A.-J. ; Cserjesi, P. ; Kanter, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4682-6af1e8d5058068213d7def312397dddc0296f45691c69daddf683fb17acaa60a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Chick Embryo - cytology</topic><topic>Chick Embryo - metabolism</topic><topic>Gonadotropin-Releasing Hormone - metabolism</topic><topic>LHRH</topic><topic>neuronal migration</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Prosencephalon - embryology</topic><topic>reproduction</topic><topic>Respiratory System - embryology</topic><topic>retrovirus</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silverman, A.-J.</creatorcontrib><creatorcontrib>Cserjesi, P.</creatorcontrib><creatorcontrib>Kanter, E.</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>MEDLINE - Academic</collection><jtitle>Journal of neuroendocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silverman, A.-J.</au><au>Cserjesi, P.</au><au>Kanter, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of Gonadotropin-Releasing Hormone Neurones in the Chick Forebrain is Independent of Lineage Relationships Among Cells of the Early Nasal Placode</atitle><jtitle>Journal of neuroendocrinology</jtitle><addtitle>J Neuroendocrinol</addtitle><date>2002-03</date><risdate>2002</risdate><volume>14</volume><issue>3</issue><spage>207</spage><epage>212</epage><pages>207-212</pages><issn>0953-8194</issn><eissn>1365-2826</eissn><abstract>The regulation of reproduction depends upon the successful migration of gonadotropin‐releasing hormone (GnRH) neurones from the nasal placode to the ventral forebrain during embryogenesis. Within the central nervous system (CNS), these neurones migrate to stereotyped, highly reproducible locations in septal, preoptic and hypothalamic nuclei. We postulated that lineage relationships (descent from a common precursor) might predict the final location of these neurones. To test this hypothesis, a complex retroviral library was used to label dividing cells in the placode and subsequently to identify them by the presence of the alkaline phosphatase marker. GnRH was detected immunocytochemically and lineage relationships determined by single cell polymerase chain reaction and sequencing of the degenerate oligonucleotide component of the retrovirus. GnRH‐positive and GnRH‐negative neurones were confined to the side ipsilateral to the injection; many cells derived from the placode that entered the CNS did not contain GnRH. This precise method of identifying and mapping the progeny of single neurones revealed that GnRH cells in any given area were derived from multiple precursors. This developmental pattern may contribute to assuring that all CNS locations critical to the orchestration of reproductive events will be populated by GnRH neurones.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><pmid>11999720</pmid><doi>10.1046/j.0007-1331.2001.00762.x</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Cell Line Chick Embryo - cytology Chick Embryo - metabolism Gonadotropin-Releasing Hormone - metabolism LHRH neuronal migration Neurons - cytology Neurons - metabolism Prosencephalon - embryology reproduction Respiratory System - embryology retrovirus Tissue Distribution |
title | Distribution of Gonadotropin-Releasing Hormone Neurones in the Chick Forebrain is Independent of Lineage Relationships Among Cells of the Early Nasal Placode |
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