bcl-2 Transgene Expression can Protect Neurons Against Developmental and Induced Cell Death
The bcl-2 protooncogene, which protects various cell types from apoptotic cell death, is expressed in the developing and adult nervous system. To explore its role in regulation of neuronal cell death, we generated transgenic mice expressing Bcl-2 under the control of the neuron-specific enolase prom...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1995-05, Vol.92 (10), p.4397-4401 |
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description | The bcl-2 protooncogene, which protects various cell types from apoptotic cell death, is expressed in the developing and adult nervous system. To explore its role in regulation of neuronal cell death, we generated transgenic mice expressing Bcl-2 under the control of the neuron-specific enolase promoter, which forced expression uniquely in neurons. Sensory neurons isolated from dorsal root ganglia of newborn mice normally require nerve growth factor for their survival in culture, but those from the bcl-2 transgenic mice showed enhanced survival in its absence. Furthermore, apoptotic death of motor neurons after axotomy of the sciatic nerve was inhibited in these mice. The number of neurons in two neuronal populations from the central and peripheral nervous system was increased by 30%, indicating that Bcl-2 expression can protect neurons from cell death during development. The generation of these transgenic mice suggests that Bcl-2 may play an important role in survival of neurons both during development and throughout adult life. |
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To explore its role in regulation of neuronal cell death, we generated transgenic mice expressing Bcl-2 under the control of the neuron-specific enolase promoter, which forced expression uniquely in neurons. Sensory neurons isolated from dorsal root ganglia of newborn mice normally require nerve growth factor for their survival in culture, but those from the bcl-2 transgenic mice showed enhanced survival in its absence. Furthermore, apoptotic death of motor neurons after axotomy of the sciatic nerve was inhibited in these mice. The number of neurons in two neuronal populations from the central and peripheral nervous system was increased by 30%, indicating that Bcl-2 expression can protect neurons from cell death during development. The generation of these transgenic mice suggests that Bcl-2 may play an important role in survival of neurons both during development and throughout adult life.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.92.10.4397</identifier><identifier>PMID: 7753817</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Aging - physiology ; Animals ; Animals, Newborn ; Apoptosis ; Brain ; Brain - cytology ; Brain - physiology ; Cell death ; Cell lines ; Cells ; Cellular biology ; Ganglia, Spinal - cytology ; Ganglia, Spinal - physiology ; Gene Expression ; Genes ; Humans ; Mice ; Mice, Transgenic ; Motor neurons ; Motor Neurons - cytology ; Motor Neurons - physiology ; Neurology ; Neurons ; Neurons - cytology ; Neurons - physiology ; Neurons, Afferent - cytology ; Neurons, Afferent - physiology ; Promoter Regions, Genetic ; Protein-Tyrosine Kinases - biosynthesis ; Proto-Oncogene Proteins - biosynthesis ; Proto-Oncogene Proteins c-bcl-2 ; Proto-Oncogenes ; Rodents ; Sciatic Nerve - physiology ; Sensory neurons ; Spinal Cord - cytology ; Spinal Cord - physiology ; Transgenes ; Transgenic animals</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1995-05, Vol.92 (10), p.4397-4401</ispartof><rights>Copyright 1995 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences May 9, 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c586t-9a66da8f9b49539ba99fa6ae8eb728543de0e6101e2d18ad297749ed1f8486ba3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/92/10.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2367334$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2367334$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7753817$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Farlie, Peter G.</creatorcontrib><creatorcontrib>Dringen, Ralf</creatorcontrib><creatorcontrib>Rees, Sandra M.</creatorcontrib><creatorcontrib>Kannourakis, George</creatorcontrib><creatorcontrib>Bernard, Ora</creatorcontrib><title>bcl-2 Transgene Expression can Protect Neurons Against Developmental and Induced Cell Death</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The bcl-2 protooncogene, which protects various cell types from apoptotic cell death, is expressed in the developing and adult nervous system. To explore its role in regulation of neuronal cell death, we generated transgenic mice expressing Bcl-2 under the control of the neuron-specific enolase promoter, which forced expression uniquely in neurons. Sensory neurons isolated from dorsal root ganglia of newborn mice normally require nerve growth factor for their survival in culture, but those from the bcl-2 transgenic mice showed enhanced survival in its absence. Furthermore, apoptotic death of motor neurons after axotomy of the sciatic nerve was inhibited in these mice. The number of neurons in two neuronal populations from the central and peripheral nervous system was increased by 30%, indicating that Bcl-2 expression can protect neurons from cell death during development. The generation of these transgenic mice suggests that Bcl-2 may play an important role in survival of neurons both during development and throughout adult life.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Apoptosis</subject><subject>Brain</subject><subject>Brain - cytology</subject><subject>Brain - physiology</subject><subject>Cell death</subject><subject>Cell lines</subject><subject>Cells</subject><subject>Cellular biology</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - physiology</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Motor neurons</subject><subject>Motor Neurons - cytology</subject><subject>Motor Neurons - physiology</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>Neurons, Afferent - cytology</subject><subject>Neurons, Afferent - physiology</subject><subject>Promoter Regions, Genetic</subject><subject>Protein-Tyrosine Kinases - biosynthesis</subject><subject>Proto-Oncogene Proteins - biosynthesis</subject><subject>Proto-Oncogene Proteins c-bcl-2</subject><subject>Proto-Oncogenes</subject><subject>Rodents</subject><subject>Sciatic Nerve - physiology</subject><subject>Sensory neurons</subject><subject>Spinal Cord - cytology</subject><subject>Spinal Cord - physiology</subject><subject>Transgenes</subject><subject>Transgenic animals</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkbtvFDEQxi0ECkegpgFkUUC1F7_WD4kmOgJEioAiVBSWd3f2sqc9-7C9Ufjv8eqO41FANRp9v280Mx9CTylZUqL42c67tDSsNEvBjbqHFpQYWklhyH20IISpSgsmHqJHKW0IIabW5ASdKFVzTdUCfW3asWL4Ojqf1uABX9ztIqQ0BI9b5_HnGDK0GX-EKQaf8PnaDT5l_BZuYQy7LfjsRux8hy99N7XQ4RWMY5FdvnmMHvRuTPDkUE_Rl3cX16sP1dWn95er86uqrbXMlXFSdk73phGm5qZxxvROOtDQKKZrwTsgICmhwDqqXceMUsJAR3sttGwcP0Vv9nN3U7OFri07RTfaXRy2Ln63wQ32T8UPN3Ydbq2gpqbF_upgj-HbBCnb7ZDacoXzEKZklWJKS6r_C1JpZG2kKODLv8BNmKIvP7CMUE4YJ6ZAZ3uojSGlCP1xYUrsnK2ds7WGzf2cbXE8__3OI38Is-ivD_ps_Kn-GmD7aRwz3OVCvvgnWYBne2CTcohHgnGpOBf8BxFrwg8</recordid><startdate>19950509</startdate><enddate>19950509</enddate><creator>Farlie, Peter G.</creator><creator>Dringen, Ralf</creator><creator>Rees, Sandra M.</creator><creator>Kannourakis, George</creator><creator>Bernard, Ora</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19950509</creationdate><title>bcl-2 Transgene Expression can Protect Neurons Against Developmental and Induced Cell Death</title><author>Farlie, Peter G. ; Dringen, Ralf ; Rees, Sandra M. ; Kannourakis, George ; Bernard, Ora</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c586t-9a66da8f9b49539ba99fa6ae8eb728543de0e6101e2d18ad297749ed1f8486ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Apoptosis</topic><topic>Brain</topic><topic>Brain - cytology</topic><topic>Brain - physiology</topic><topic>Cell death</topic><topic>Cell lines</topic><topic>Cells</topic><topic>Cellular biology</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - physiology</topic><topic>Gene Expression</topic><topic>Genes</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Motor neurons</topic><topic>Motor Neurons - cytology</topic><topic>Motor Neurons - physiology</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Neurons, Afferent - cytology</topic><topic>Neurons, Afferent - physiology</topic><topic>Promoter Regions, Genetic</topic><topic>Protein-Tyrosine Kinases - biosynthesis</topic><topic>Proto-Oncogene Proteins - biosynthesis</topic><topic>Proto-Oncogene Proteins c-bcl-2</topic><topic>Proto-Oncogenes</topic><topic>Rodents</topic><topic>Sciatic Nerve - physiology</topic><topic>Sensory neurons</topic><topic>Spinal Cord - cytology</topic><topic>Spinal Cord - physiology</topic><topic>Transgenes</topic><topic>Transgenic animals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farlie, Peter G.</creatorcontrib><creatorcontrib>Dringen, Ralf</creatorcontrib><creatorcontrib>Rees, Sandra M.</creatorcontrib><creatorcontrib>Kannourakis, George</creatorcontrib><creatorcontrib>Bernard, Ora</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farlie, Peter G.</au><au>Dringen, Ralf</au><au>Rees, Sandra M.</au><au>Kannourakis, George</au><au>Bernard, Ora</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>bcl-2 Transgene Expression can Protect Neurons Against Developmental and Induced Cell Death</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1995-05-09</date><risdate>1995</risdate><volume>92</volume><issue>10</issue><spage>4397</spage><epage>4401</epage><pages>4397-4401</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The bcl-2 protooncogene, which protects various cell types from apoptotic cell death, is expressed in the developing and adult nervous system. To explore its role in regulation of neuronal cell death, we generated transgenic mice expressing Bcl-2 under the control of the neuron-specific enolase promoter, which forced expression uniquely in neurons. Sensory neurons isolated from dorsal root ganglia of newborn mice normally require nerve growth factor for their survival in culture, but those from the bcl-2 transgenic mice showed enhanced survival in its absence. Furthermore, apoptotic death of motor neurons after axotomy of the sciatic nerve was inhibited in these mice. The number of neurons in two neuronal populations from the central and peripheral nervous system was increased by 30%, indicating that Bcl-2 expression can protect neurons from cell death during development. The generation of these transgenic mice suggests that Bcl-2 may play an important role in survival of neurons both during development and throughout adult life.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>7753817</pmid><doi>10.1073/pnas.92.10.4397</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging - physiology Animals Animals, Newborn Apoptosis Brain Brain - cytology Brain - physiology Cell death Cell lines Cells Cellular biology Ganglia, Spinal - cytology Ganglia, Spinal - physiology Gene Expression Genes Humans Mice Mice, Transgenic Motor neurons Motor Neurons - cytology Motor Neurons - physiology Neurology Neurons Neurons - cytology Neurons - physiology Neurons, Afferent - cytology Neurons, Afferent - physiology Promoter Regions, Genetic Protein-Tyrosine Kinases - biosynthesis Proto-Oncogene Proteins - biosynthesis Proto-Oncogene Proteins c-bcl-2 Proto-Oncogenes Rodents Sciatic Nerve - physiology Sensory neurons Spinal Cord - cytology Spinal Cord - physiology Transgenes Transgenic animals |
title | bcl-2 Transgene Expression can Protect Neurons Against Developmental and Induced Cell Death |
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