Cytokine-Induced Nuclear Factor Kappa B Activation Promotes the Survival of Developing Neurons
Ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), cardiotrophin-1 (CT-1), and interleukin 6 (IL-6) comprise a group of structurally related cytokines that promote the survival of subsets of neurons in the developing peripheral nervous system, but the signaling pathways activated...
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Veröffentlicht in: | The Journal of cell biology 2000-01, Vol.148 (2), p.325-332 |
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creator | Middleton, Gayle Hamanoue, Makoto Enokido, Yasushi Wyatt, Sean Pennica, Diane Jaffray, Ellis Hay, Ronald T. Davies, Alun M. |
description | Ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), cardiotrophin-1 (CT-1), and interleukin 6 (IL-6) comprise a group of structurally related cytokines that promote the survival of subsets of neurons in the developing peripheral nervous system, but the signaling pathways activated by these cytokines that prevent neuronal apoptosis are unclear. Here, we show that these cytokines activate NF-κB in cytokine-dependent developing sensory neurons. Preventing NF-κB activation with a super-repressor IκB-α protein markedly reduces the number of neurons that survive in the presence of cytokines, but has no effect on the survival response of the same neurons to brain-derived neurotrophic factors (BDNF), an unrelated neurotrophic factor that binds to a different class of receptors. Cytokine-dependent sensory neurons cultured from embryos that lack p65, a transcriptionally active subunit of NF-κB, have a markedly impaired ability to survive in response to cytokines, but respond normally to BDNF. There is increased apoptosis of cytokine-dependent neurons in p65-/-embryos in vivo, resulting in a reduction in the total number of these neurons compared with their numbers in wild-type embryos. These results demonstrate that NF-κB plays a key role in mediating the survival response of developing neurons to cytokines. |
doi_str_mv | 10.1083/jcb.148.2.325 |
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Here, we show that these cytokines activate NF-κB in cytokine-dependent developing sensory neurons. Preventing NF-κB activation with a super-repressor IκB-α protein markedly reduces the number of neurons that survive in the presence of cytokines, but has no effect on the survival response of the same neurons to brain-derived neurotrophic factors (BDNF), an unrelated neurotrophic factor that binds to a different class of receptors. Cytokine-dependent sensory neurons cultured from embryos that lack p65, a transcriptionally active subunit of NF-κB, have a markedly impaired ability to survive in response to cytokines, but respond normally to BDNF. There is increased apoptosis of cytokine-dependent neurons in p65-/-embryos in vivo, resulting in a reduction in the total number of these neurons compared with their numbers in wild-type embryos. These results demonstrate that NF-κB plays a key role in mediating the survival response of developing neurons to cytokines.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.148.2.325</identifier><identifier>PMID: 10648565</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>United States: Rockefeller University Press</publisher><subject>Apoptosis ; brain-derived neurotrophic factor ; cardiotrophin 1 ; Cell Survival ; Cellular biology ; Ciliary neurotrophic factor ; Ciliary Neurotrophic Factor - pharmacology ; Cytokine receptors ; Cytokines ; Cytokines - pharmacology ; Embryos ; Ganglia, Sensory - cytology ; Ganglia, Sensory - drug effects ; Ganglia, Sensory - embryology ; Ganglia, Sensory - metabolism ; Genes ; Growth Inhibitors - pharmacology ; I^KB^a protein ; Interleukin-6 - pharmacology ; Leukemia ; Leukemia Inhibitory Factor ; Lymphokines - pharmacology ; Neurons ; Neurons - drug effects ; Neurons - metabolism ; NF-^KB protein ; NF-kappa B - metabolism ; Nodose ganglion ; Nodose Ganglion - cytology ; Nodose Ganglion - drug effects ; Nodose Ganglion - embryology ; Nodose Ganglion - metabolism ; Original ; Plasmids ; Receptors ; Receptors, Cytokine - biosynthesis ; Sensory neurons ; Trigeminal Ganglion - cytology ; Trigeminal Ganglion - drug effects ; Trigeminal Ganglion - metabolism</subject><ispartof>The Journal of cell biology, 2000-01, Vol.148 (2), p.325-332</ispartof><rights>Copyright 2000 The Rockefeller University Press</rights><rights>Copyright Rockefeller University Press Jan 24, 2000</rights><rights>2000 The Rockefeller University Press 2000 The Rockefeller University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-d56ea63eee8f3e460ba997214955908ad20addb112dae57e9d3c5fb418d9c1263</citedby><cites>FETCH-LOGICAL-c462t-d56ea63eee8f3e460ba997214955908ad20addb112dae57e9d3c5fb418d9c1263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10648565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Middleton, Gayle</creatorcontrib><creatorcontrib>Hamanoue, Makoto</creatorcontrib><creatorcontrib>Enokido, Yasushi</creatorcontrib><creatorcontrib>Wyatt, Sean</creatorcontrib><creatorcontrib>Pennica, Diane</creatorcontrib><creatorcontrib>Jaffray, Ellis</creatorcontrib><creatorcontrib>Hay, Ronald T.</creatorcontrib><creatorcontrib>Davies, Alun M.</creatorcontrib><title>Cytokine-Induced Nuclear Factor Kappa B Activation Promotes the Survival of Developing Neurons</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), cardiotrophin-1 (CT-1), and interleukin 6 (IL-6) comprise a group of structurally related cytokines that promote the survival of subsets of neurons in the developing peripheral nervous system, but the signaling pathways activated by these cytokines that prevent neuronal apoptosis are unclear. Here, we show that these cytokines activate NF-κB in cytokine-dependent developing sensory neurons. Preventing NF-κB activation with a super-repressor IκB-α protein markedly reduces the number of neurons that survive in the presence of cytokines, but has no effect on the survival response of the same neurons to brain-derived neurotrophic factors (BDNF), an unrelated neurotrophic factor that binds to a different class of receptors. Cytokine-dependent sensory neurons cultured from embryos that lack p65, a transcriptionally active subunit of NF-κB, have a markedly impaired ability to survive in response to cytokines, but respond normally to BDNF. There is increased apoptosis of cytokine-dependent neurons in p65-/-embryos in vivo, resulting in a reduction in the total number of these neurons compared with their numbers in wild-type embryos. These results demonstrate that NF-κB plays a key role in mediating the survival response of developing neurons to cytokines.</description><subject>Apoptosis</subject><subject>brain-derived neurotrophic factor</subject><subject>cardiotrophin 1</subject><subject>Cell Survival</subject><subject>Cellular biology</subject><subject>Ciliary neurotrophic factor</subject><subject>Ciliary Neurotrophic Factor - pharmacology</subject><subject>Cytokine receptors</subject><subject>Cytokines</subject><subject>Cytokines - pharmacology</subject><subject>Embryos</subject><subject>Ganglia, Sensory - cytology</subject><subject>Ganglia, Sensory - drug effects</subject><subject>Ganglia, Sensory - embryology</subject><subject>Ganglia, Sensory - metabolism</subject><subject>Genes</subject><subject>Growth Inhibitors - pharmacology</subject><subject>I^KB^a protein</subject><subject>Interleukin-6 - pharmacology</subject><subject>Leukemia</subject><subject>Leukemia Inhibitory Factor</subject><subject>Lymphokines - pharmacology</subject><subject>Neurons</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>NF-^KB protein</subject><subject>NF-kappa B - metabolism</subject><subject>Nodose ganglion</subject><subject>Nodose Ganglion - cytology</subject><subject>Nodose Ganglion - drug effects</subject><subject>Nodose Ganglion - embryology</subject><subject>Nodose Ganglion - metabolism</subject><subject>Original</subject><subject>Plasmids</subject><subject>Receptors</subject><subject>Receptors, Cytokine - biosynthesis</subject><subject>Sensory neurons</subject><subject>Trigeminal Ganglion - cytology</subject><subject>Trigeminal Ganglion - drug effects</subject><subject>Trigeminal Ganglion - metabolism</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFvFCEUh4nR2G316M0Y4qG3WYEBhrmY1NVq06Y2qV4lDLxpZ52FEZhN-t_LZhtbvXh6h9-XH-_xIfSKkiUlqn63tt2ScrVky5qJJ2hBBSeVopw8RQtCGK1awcQBOkxpTQjhDa-fowNKJFdCigX6sbrL4efgoTrzbrbg8OVsRzARnxqbQ8TnZpoM_oBPbB62Jg_B46sYNiFDwvkW8PUctyUYcejxR9jCGKbB3-BLmGPw6QV61psxwcv7eYS-n376tvpSXXz9fLY6uagslyxXTkgwsgYA1dfAJelM2zaM8laIlijjGDHOdZQyZ0A00Lrair7jVLnWUibrI_R-3zvN3QacBZ-jGfUUh42JdzqYQf-d-OFW34StZrThTJFScHxfEMOvGVLWmyFZGEfjIcxJN0Q1ssD_BUtfWbzegW__Addhjr78wu5RogSTokDVHrIxpBSh_7MyJXrnVxe_uvjVTBe_hX_z-M5H9F5oAV7vgXUq9h5ySVtJeP0blJerag</recordid><startdate>20000124</startdate><enddate>20000124</enddate><creator>Middleton, Gayle</creator><creator>Hamanoue, Makoto</creator><creator>Enokido, Yasushi</creator><creator>Wyatt, Sean</creator><creator>Pennica, Diane</creator><creator>Jaffray, Ellis</creator><creator>Hay, Ronald T.</creator><creator>Davies, Alun M.</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</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>20000124</creationdate><title>Cytokine-Induced Nuclear Factor Kappa B Activation Promotes the Survival of Developing Neurons</title><author>Middleton, Gayle ; Hamanoue, Makoto ; Enokido, Yasushi ; Wyatt, Sean ; Pennica, Diane ; Jaffray, Ellis ; Hay, Ronald T. ; Davies, Alun M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-d56ea63eee8f3e460ba997214955908ad20addb112dae57e9d3c5fb418d9c1263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Apoptosis</topic><topic>brain-derived neurotrophic factor</topic><topic>cardiotrophin 1</topic><topic>Cell Survival</topic><topic>Cellular biology</topic><topic>Ciliary neurotrophic factor</topic><topic>Ciliary Neurotrophic Factor - pharmacology</topic><topic>Cytokine receptors</topic><topic>Cytokines</topic><topic>Cytokines - pharmacology</topic><topic>Embryos</topic><topic>Ganglia, Sensory - cytology</topic><topic>Ganglia, Sensory - drug effects</topic><topic>Ganglia, Sensory - embryology</topic><topic>Ganglia, Sensory - metabolism</topic><topic>Genes</topic><topic>Growth Inhibitors - pharmacology</topic><topic>I^KB^a protein</topic><topic>Interleukin-6 - pharmacology</topic><topic>Leukemia</topic><topic>Leukemia Inhibitory Factor</topic><topic>Lymphokines - pharmacology</topic><topic>Neurons</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>NF-^KB protein</topic><topic>NF-kappa B - metabolism</topic><topic>Nodose ganglion</topic><topic>Nodose Ganglion - cytology</topic><topic>Nodose Ganglion - drug effects</topic><topic>Nodose Ganglion - embryology</topic><topic>Nodose Ganglion - metabolism</topic><topic>Original</topic><topic>Plasmids</topic><topic>Receptors</topic><topic>Receptors, Cytokine - biosynthesis</topic><topic>Sensory neurons</topic><topic>Trigeminal Ganglion - cytology</topic><topic>Trigeminal Ganglion - drug effects</topic><topic>Trigeminal Ganglion - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Middleton, Gayle</creatorcontrib><creatorcontrib>Hamanoue, Makoto</creatorcontrib><creatorcontrib>Enokido, Yasushi</creatorcontrib><creatorcontrib>Wyatt, Sean</creatorcontrib><creatorcontrib>Pennica, Diane</creatorcontrib><creatorcontrib>Jaffray, Ellis</creatorcontrib><creatorcontrib>Hay, Ronald T.</creatorcontrib><creatorcontrib>Davies, Alun M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids 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>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Middleton, Gayle</au><au>Hamanoue, Makoto</au><au>Enokido, Yasushi</au><au>Wyatt, Sean</au><au>Pennica, Diane</au><au>Jaffray, Ellis</au><au>Hay, Ronald T.</au><au>Davies, Alun M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine-Induced Nuclear Factor Kappa B Activation Promotes the Survival of Developing Neurons</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>2000-01-24</date><risdate>2000</risdate><volume>148</volume><issue>2</issue><spage>325</spage><epage>332</epage><pages>325-332</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), cardiotrophin-1 (CT-1), and interleukin 6 (IL-6) comprise a group of structurally related cytokines that promote the survival of subsets of neurons in the developing peripheral nervous system, but the signaling pathways activated by these cytokines that prevent neuronal apoptosis are unclear. Here, we show that these cytokines activate NF-κB in cytokine-dependent developing sensory neurons. Preventing NF-κB activation with a super-repressor IκB-α protein markedly reduces the number of neurons that survive in the presence of cytokines, but has no effect on the survival response of the same neurons to brain-derived neurotrophic factors (BDNF), an unrelated neurotrophic factor that binds to a different class of receptors. Cytokine-dependent sensory neurons cultured from embryos that lack p65, a transcriptionally active subunit of NF-κB, have a markedly impaired ability to survive in response to cytokines, but respond normally to BDNF. There is increased apoptosis of cytokine-dependent neurons in p65-/-embryos in vivo, resulting in a reduction in the total number of these neurons compared with their numbers in wild-type embryos. These results demonstrate that NF-κB plays a key role in mediating the survival response of developing neurons to cytokines.</abstract><cop>United States</cop><pub>Rockefeller University Press</pub><pmid>10648565</pmid><doi>10.1083/jcb.148.2.325</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis brain-derived neurotrophic factor cardiotrophin 1 Cell Survival Cellular biology Ciliary neurotrophic factor Ciliary Neurotrophic Factor - pharmacology Cytokine receptors Cytokines Cytokines - pharmacology Embryos Ganglia, Sensory - cytology Ganglia, Sensory - drug effects Ganglia, Sensory - embryology Ganglia, Sensory - metabolism Genes Growth Inhibitors - pharmacology I^KB^a protein Interleukin-6 - pharmacology Leukemia Leukemia Inhibitory Factor Lymphokines - pharmacology Neurons Neurons - drug effects Neurons - metabolism NF-^KB protein NF-kappa B - metabolism Nodose ganglion Nodose Ganglion - cytology Nodose Ganglion - drug effects Nodose Ganglion - embryology Nodose Ganglion - metabolism Original Plasmids Receptors Receptors, Cytokine - biosynthesis Sensory neurons Trigeminal Ganglion - cytology Trigeminal Ganglion - drug effects Trigeminal Ganglion - metabolism |
title | Cytokine-Induced Nuclear Factor Kappa B Activation Promotes the Survival of Developing Neurons |
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