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Mol Cell Neurosci. 2008 Aug;38(4):518-25. doi: 10.1016/j.mcn.2008.04.013. Epub 2008 May 11.

A novel role for jun N-terminal kinase signaling in olfactory sensory neuronal death.

Author information

1
Department of Biological Sciences, Columbia University, NY, NY, USA.

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.

PMID:
18571430
PMCID:
PMC2568995
DOI:
10.1016/j.mcn.2008.04.013
[Indexed for MEDLINE]
Free PMC Article

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