| Literature DB >> 11849756 |
Linda Trotter1, Wendy Panton, Iradj Hajimohamadreza, Lawrence Petalidis, Robin Ward, Yvonne Fleming, Christopher G Armstrong, Philip Cohen, Eric H Karran, Ross A Kinloch.
Abstract
A stress-activated protein kinase pathway comprising mitogen-activated protein kinase kinases (MKKs), c-Jun N-terminal kinase (JNK) and the transcription factor c-Jun is implicated in neuronal apoptosis. Using an immune-complex kinase assay, we measured the activation of MKK4 and MKK7 in low potassium (LK)-induced apoptosis of rat cerebellar granule neurons (CGN). MKK7, but not MKK4, was activated within the first 4-6 h in four independent sets of 14-h CGN apoptosis time-courses. CEP-1347 (500 nM), an mixed-lineage kinase 3 inhibitor, prevented MKK7 activation and cell death following exposure of CGN cultures to LK-induced apoptosis. Western blot analysis revealed that levels of phosphorylated c-Jun were elevated between 30 min and 10 h of CGN apoptosis, temporally consistent with MKK7 activation. These data suggest that MKK7 is responsible for activating the JNK pathway during LK-induced CGN apoptosis.Entities:
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Year: 2002 PMID: 11849756 DOI: 10.1016/s0304-3940(02)00005-8
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046