Decreased apoptosome activity with neuronal differentiation sets the threshold for strict IAP regulation of apoptosis

Kevin M. Wright, Michael W. Linhoff, Patrick Ryan Potts, Mohanish Deshmukh

Research output: Contribution to journalArticle

68 Scopus citations

Abstract

Despite the potential of the inhibitor of apoptosis proteins (IAPs) to block cytochrome c-dependent caspase activation, the critical function of IAPs in regulating mammalian apoptosis remains unclear. We report that the ability of endogenous IAPs to effectively regulate caspase activation depends on the differentiation state of the cell. Despite being expressed at equivalent levels, endogenous IAPs afforded no protection against cytochrome c-induced apoptosis in naïve pheochromocytoma (PC12) cells, but were remarkably effective in doing so in neuronally differentiated cells. Neuronal differentiation was also accompanied with a marked reduction in Apaf-1, resulting in a significant decrease in apoptosome activity. Importantly, this decrease in Apaf-1 protein was directly linked to the increased ability of IAPs to stringently regulate apoptosis in neuronally differentiated PC12 and primary cells. These data illustrate specifically how the apoptotic pathway acquires increased regulation with cellular differentiation, and are the first to show that IAP function and apoptosome activity are coupled in cells.

Original languageEnglish (US)
Pages (from-to)303-313
Number of pages11
JournalJournal of Cell Biology
Volume167
Issue number2
DOIs
StatePublished - Oct 25 2004

ASJC Scopus subject areas

  • Cell Biology

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