Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2001-4-13
pubmed:abstractText
Sympathetic neurons require nerve growth factor for survival and die by apoptosis in its absence. Key steps in the death pathway include c-Jun activation, mitochondrial cytochrome c release, and caspase activation. Here, we show that neurons rescued from NGF withdrawal-induced apoptosis by expression of dominant-negative c-Jun do not release cytochrome c from their mitochondria. Furthermore, we find that the mRNA for BIM(EL), a proapoptotic BCL-2 family member, increases in level after NGF withdrawal and that this is reduced by dominant-negative c-Jun. Finally, overexpression of BIM(EL) in neurons induces cytochrome c redistribution and apoptosis in the presence of NGF, and neurons injected with Bim antisense oligonucleotides or isolated from Bim(-/-) knockout mice die more slowly after NGF withdrawal.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Apoptosis Regulatory Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Bcl-2-like protein 11, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome c Group, http://linkedlifedata.com/resource/pubmed/chemical/MAP Kinase Kinase Kinase 1, http://linkedlifedata.com/resource/pubmed/chemical/Map3k1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Oligonucleotides, Antisense, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-jun
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0896-6273
pubmed:author
pubmed:issnType
Print
pubmed:volume
29
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
629-43
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:11301023-Adenoviridae, pubmed-meshheading:11301023-Animals, pubmed-meshheading:11301023-Apoptosis, pubmed-meshheading:11301023-Apoptosis Regulatory Proteins, pubmed-meshheading:11301023-Carrier Proteins, pubmed-meshheading:11301023-Caspases, pubmed-meshheading:11301023-Cell Survival, pubmed-meshheading:11301023-Cells, Cultured, pubmed-meshheading:11301023-Cytochrome c Group, pubmed-meshheading:11301023-Enzyme Activation, pubmed-meshheading:11301023-Gene Expression, pubmed-meshheading:11301023-MAP Kinase Kinase Kinase 1, pubmed-meshheading:11301023-Membrane Proteins, pubmed-meshheading:11301023-Mice, pubmed-meshheading:11301023-Mice, Knockout, pubmed-meshheading:11301023-Microinjections, pubmed-meshheading:11301023-Mitochondria, pubmed-meshheading:11301023-Nerve Growth Factor, pubmed-meshheading:11301023-Neurons, pubmed-meshheading:11301023-Oligonucleotides, Antisense, pubmed-meshheading:11301023-Protein-Serine-Threonine Kinases, pubmed-meshheading:11301023-Proto-Oncogene Proteins, pubmed-meshheading:11301023-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:11301023-Proto-Oncogene Proteins c-jun, pubmed-meshheading:11301023-Rats, pubmed-meshheading:11301023-Rats, Sprague-Dawley, pubmed-meshheading:11301023-Superior Cervical Ganglion, pubmed-meshheading:11301023-Transfection
pubmed:year
2001
pubmed:articleTitle
Dominant-negative c-Jun promotes neuronal survival by reducing BIM expression and inhibiting mitochondrial cytochrome c release.
pubmed:affiliation
Eisai London Research Laboratories, Bernard Katz Building, University College London, Gower Street, WC1E 6BT, London, United Kingdom.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't