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pubmed-article:11301023pubmed:abstractTextSympathetic 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.lld:pubmed
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pubmed-article:11301023pubmed:year2001lld:pubmed
pubmed-article:11301023pubmed:articleTitleDominant-negative c-Jun promotes neuronal survival by reducing BIM expression and inhibiting mitochondrial cytochrome c release.lld:pubmed
pubmed-article:11301023pubmed:affiliationEisai London Research Laboratories, Bernard Katz Building, University College London, Gower Street, WC1E 6BT, London, United Kingdom.lld:pubmed
pubmed-article:11301023pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11301023pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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