Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat
Programmed cell death has been demonstrated in several specific neuronal populations as a mechanism for modulating the population size following differentiation, but its applicability to all neuronal types is unclear. Evidence for programmed cell death in some populations such as the numerous spinal...
Gespeichert in:
Veröffentlicht in: | The European journal of neuroscience 1997-04, Vol.9 (4), p.794-799 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 799 |
---|---|
container_issue | 4 |
container_start_page | 794 |
container_title | The European journal of neuroscience |
container_volume | 9 |
creator | Lawson, S. J. Davies, H. J. Bennett, J. P. Lowrie, M. B. |
description | Programmed cell death has been demonstrated in several specific neuronal populations as a mechanism for modulating the population size following differentiation, but its applicability to all neuronal types is unclear. Evidence for programmed cell death in some populations such as the numerous spinal interneurons has been lacking. We have studied the incidence of apoptosis in the rat spinal cord with three different methods and found a previously undocumented wave of apoptosis occurring in spinal grey matter shortly after birth. The apoptotic morphology was confirmed ultrastructurally. Dying cells were identified as neurons by immunocytochemical labelling for neuronal markers and had an anatomical distribution which indicated that most of the apoptotic cells were interneurons not motoneurons. This wave of apoptosis has the characteristics of a discrete developmental process and occurs later than that of either ventral horn motoneurons or dorsal root ganglion cells, to which most spinal interneurons are connected. These findings indicate that interneurons do undergo programmed cell death, and we suggest that this occurs in response to the earlier reduction in size of their main synaptic targets. |
doi_str_mv | 10.1111/j.1460-9568.1997.tb01428.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79016221</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20973834</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4714-e4fe3cb47f598f8754d9b9fb2527cd1aab71c453819bae5dd143368034b4d7d53</originalsourceid><addsrcrecordid>eNqVkcFv0zAUxi0EGmXwJyBZHBCXZHZsxzYHpKl0Y6gqE-sYN8uJX9aUNCm2O9r_fola9ci0d3mH73vfs98PoQ-UpLSvs2VKeU4SLXKVUq1lGgtCeabS7Qs0Okov0YhowRJF89-v0ZsQloQQlXNxgk40FUyofIR-TR5qB20JeL6wEd-s69Y2-KqN4FvY-K4N-LZ14O87fO27e29XK3B4DE2Dv4KNC3zdhdjaaJtmh-sWxwXgnza-Ra8q2wR4d-in6PZiMh9_S6Y_Lq_G59Ok5JLyBHgFrCy4rIRWlZKCO13oqshEJktHrS0kLblgiurCgnCOcsZyRRgvuJNOsFP0cZ-79t3fDYRoVnUo-9fZFrpNMFITmmcZfdKYES2ZYrw3fvqvkSqiJCOaD8s_762l70LwUJm1r1fW7wwlZgBllmagYQYaZgBlDqDMth9-f9izKfqTHkcPZHr9y17_Vzewe0aymXyfST18JNkH1CHC9hhg_R-TSyaFuZtdmv6a-m56Mzcz9ggHxbG_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1808730945</pqid></control><display><type>article</type><title>Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Lawson, S. J. ; Davies, H. J. ; Bennett, J. P. ; Lowrie, M. B.</creator><creatorcontrib>Lawson, S. J. ; Davies, H. J. ; Bennett, J. P. ; Lowrie, M. B.</creatorcontrib><description>Programmed cell death has been demonstrated in several specific neuronal populations as a mechanism for modulating the population size following differentiation, but its applicability to all neuronal types is unclear. Evidence for programmed cell death in some populations such as the numerous spinal interneurons has been lacking. We have studied the incidence of apoptosis in the rat spinal cord with three different methods and found a previously undocumented wave of apoptosis occurring in spinal grey matter shortly after birth. The apoptotic morphology was confirmed ultrastructurally. Dying cells were identified as neurons by immunocytochemical labelling for neuronal markers and had an anatomical distribution which indicated that most of the apoptotic cells were interneurons not motoneurons. This wave of apoptosis has the characteristics of a discrete developmental process and occurs later than that of either ventral horn motoneurons or dorsal root ganglion cells, to which most spinal interneurons are connected. These findings indicate that interneurons do undergo programmed cell death, and we suggest that this occurs in response to the earlier reduction in size of their main synaptic targets.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1111/j.1460-9568.1997.tb01428.x</identifier><identifier>PMID: 9153586</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aging - physiology ; Animals ; Animals, Newborn ; Apoptosis ; Biomarkers ; Embryo, Mammalian ; Fast Blue ; Gestational Age ; Microscopy, Electron ; Nerve Tissue Proteins - analysis ; Neurons - cytology ; Neurons - physiology ; Neurons - ultrastructure ; PGP9.5 ; Phosphopyruvate Hydratase - analysis ; postnatal development ; rat ; Rats ; Rats, Wistar ; Spinal Cord - embryology ; Spinal Cord - growth & development ; Spinal Cord - physiology ; Thiolester Hydrolases - analysis ; Ubiquitin Thiolesterase</subject><ispartof>The European journal of neuroscience, 1997-04, Vol.9 (4), p.794-799</ispartof><rights>European Neuroscience Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4714-e4fe3cb47f598f8754d9b9fb2527cd1aab71c453819bae5dd143368034b4d7d53</citedby><cites>FETCH-LOGICAL-c4714-e4fe3cb47f598f8754d9b9fb2527cd1aab71c453819bae5dd143368034b4d7d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1460-9568.1997.tb01428.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1460-9568.1997.tb01428.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9153586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lawson, S. J.</creatorcontrib><creatorcontrib>Davies, H. J.</creatorcontrib><creatorcontrib>Bennett, J. P.</creatorcontrib><creatorcontrib>Lowrie, M. B.</creatorcontrib><title>Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Programmed cell death has been demonstrated in several specific neuronal populations as a mechanism for modulating the population size following differentiation, but its applicability to all neuronal types is unclear. Evidence for programmed cell death in some populations such as the numerous spinal interneurons has been lacking. We have studied the incidence of apoptosis in the rat spinal cord with three different methods and found a previously undocumented wave of apoptosis occurring in spinal grey matter shortly after birth. The apoptotic morphology was confirmed ultrastructurally. Dying cells were identified as neurons by immunocytochemical labelling for neuronal markers and had an anatomical distribution which indicated that most of the apoptotic cells were interneurons not motoneurons. This wave of apoptosis has the characteristics of a discrete developmental process and occurs later than that of either ventral horn motoneurons or dorsal root ganglion cells, to which most spinal interneurons are connected. These findings indicate that interneurons do undergo programmed cell death, and we suggest that this occurs in response to the earlier reduction in size of their main synaptic targets.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Embryo, Mammalian</subject><subject>Fast Blue</subject><subject>Gestational Age</subject><subject>Microscopy, Electron</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>Neurons - ultrastructure</subject><subject>PGP9.5</subject><subject>Phosphopyruvate Hydratase - analysis</subject><subject>postnatal development</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Spinal Cord - embryology</subject><subject>Spinal Cord - growth & development</subject><subject>Spinal Cord - physiology</subject><subject>Thiolester Hydrolases - analysis</subject><subject>Ubiquitin Thiolesterase</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkcFv0zAUxi0EGmXwJyBZHBCXZHZsxzYHpKl0Y6gqE-sYN8uJX9aUNCm2O9r_fola9ci0d3mH73vfs98PoQ-UpLSvs2VKeU4SLXKVUq1lGgtCeabS7Qs0Okov0YhowRJF89-v0ZsQloQQlXNxgk40FUyofIR-TR5qB20JeL6wEd-s69Y2-KqN4FvY-K4N-LZ14O87fO27e29XK3B4DE2Dv4KNC3zdhdjaaJtmh-sWxwXgnza-Ra8q2wR4d-in6PZiMh9_S6Y_Lq_G59Ok5JLyBHgFrCy4rIRWlZKCO13oqshEJktHrS0kLblgiurCgnCOcsZyRRgvuJNOsFP0cZ-79t3fDYRoVnUo-9fZFrpNMFITmmcZfdKYES2ZYrw3fvqvkSqiJCOaD8s_762l70LwUJm1r1fW7wwlZgBllmagYQYaZgBlDqDMth9-f9izKfqTHkcPZHr9y17_Vzewe0aymXyfST18JNkH1CHC9hhg_R-TSyaFuZtdmv6a-m56Mzcz9ggHxbG_</recordid><startdate>199704</startdate><enddate>199704</enddate><creator>Lawson, S. J.</creator><creator>Davies, H. J.</creator><creator>Bennett, J. P.</creator><creator>Lowrie, M. B.</creator><general>Blackwell Publishing 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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199704</creationdate><title>Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat</title><author>Lawson, S. J. ; Davies, H. J. ; Bennett, J. P. ; Lowrie, M. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4714-e4fe3cb47f598f8754d9b9fb2527cd1aab71c453819bae5dd143368034b4d7d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Apoptosis</topic><topic>Biomarkers</topic><topic>Embryo, Mammalian</topic><topic>Fast Blue</topic><topic>Gestational Age</topic><topic>Microscopy, Electron</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Neurons - ultrastructure</topic><topic>PGP9.5</topic><topic>Phosphopyruvate Hydratase - analysis</topic><topic>postnatal development</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Spinal Cord - embryology</topic><topic>Spinal Cord - growth & development</topic><topic>Spinal Cord - physiology</topic><topic>Thiolester Hydrolases - analysis</topic><topic>Ubiquitin Thiolesterase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lawson, S. J.</creatorcontrib><creatorcontrib>Davies, H. J.</creatorcontrib><creatorcontrib>Bennett, J. P.</creatorcontrib><creatorcontrib>Lowrie, M. B.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lawson, S. J.</au><au>Davies, H. J.</au><au>Bennett, J. P.</au><au>Lowrie, M. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>1997-04</date><risdate>1997</risdate><volume>9</volume><issue>4</issue><spage>794</spage><epage>799</epage><pages>794-799</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Programmed cell death has been demonstrated in several specific neuronal populations as a mechanism for modulating the population size following differentiation, but its applicability to all neuronal types is unclear. Evidence for programmed cell death in some populations such as the numerous spinal interneurons has been lacking. We have studied the incidence of apoptosis in the rat spinal cord with three different methods and found a previously undocumented wave of apoptosis occurring in spinal grey matter shortly after birth. The apoptotic morphology was confirmed ultrastructurally. Dying cells were identified as neurons by immunocytochemical labelling for neuronal markers and had an anatomical distribution which indicated that most of the apoptotic cells were interneurons not motoneurons. This wave of apoptosis has the characteristics of a discrete developmental process and occurs later than that of either ventral horn motoneurons or dorsal root ganglion cells, to which most spinal interneurons are connected. These findings indicate that interneurons do undergo programmed cell death, and we suggest that this occurs in response to the earlier reduction in size of their main synaptic targets.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9153586</pmid><doi>10.1111/j.1460-9568.1997.tb01428.x</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0953-816X |
ispartof | The European journal of neuroscience, 1997-04, Vol.9 (4), p.794-799 |
issn | 0953-816X 1460-9568 |
language | eng |
recordid | cdi_proquest_miscellaneous_79016221 |
source | MEDLINE; Access via Wiley Online Library |
subjects | Aging - physiology Animals Animals, Newborn Apoptosis Biomarkers Embryo, Mammalian Fast Blue Gestational Age Microscopy, Electron Nerve Tissue Proteins - analysis Neurons - cytology Neurons - physiology Neurons - ultrastructure PGP9.5 Phosphopyruvate Hydratase - analysis postnatal development rat Rats Rats, Wistar Spinal Cord - embryology Spinal Cord - growth & development Spinal Cord - physiology Thiolester Hydrolases - analysis Ubiquitin Thiolesterase |
title | Evidence That Spinal Interneurons Undergo Programmed Cell Death Postnatally in the Rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T16%3A32%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evidence%20That%20Spinal%20Interneurons%20Undergo%20Programmed%20Cell%20Death%20Postnatally%20in%20the%20Rat&rft.jtitle=The%20European%20journal%20of%20neuroscience&rft.au=Lawson,%20S.%20J.&rft.date=1997-04&rft.volume=9&rft.issue=4&rft.spage=794&rft.epage=799&rft.pages=794-799&rft.issn=0953-816X&rft.eissn=1460-9568&rft_id=info:doi/10.1111/j.1460-9568.1997.tb01428.x&rft_dat=%3Cproquest_cross%3E20973834%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1808730945&rft_id=info:pmid/9153586&rfr_iscdi=true |