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• W2009548911 abstract "Olfactory sensory neurons (OSNs) represent a unique population of neurons in which death and regeneration are ongoing throughout adulthood, a feature that makes them an attractive model cell type for the investigation of neuronal death. However, the mechanism by which OSNs die remains elusive. Therefore, we developed a culture system for studying pathways involved in OSN death. Here, we show that inhibition of transcription or translation, by actinomycin D or cycloheximide, respectively, suppresses pathways leading to death, prolonging the survival of OSNs in culture. We discovered that caspase activity and jun N-terminal kinase (JNK) signaling both play a role in OSN death, and inhibition of JNK activity suppresses effector caspase (caspase-3) activation. Results from studies in culture were confirmed in vivo, in a mouse bulbectomy-induced OSN death model. These findings provide new insights into the nature of OSN death and a means of studying OSNs in vitro." @default.
• W2009548911 created "2016-06-24" @default.
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• W2009548911 date "2008-08-01" @default.
• W2009548911 modified "2023-10-16" @default.
• W2009548911 title "A novel role for jun N-terminal Kinase signaling in olfactory sensory neuronal death" @default.
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• W2009548911 doi "https://doi.org/10.1016/j.mcn.2008.04.013" @default.
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