| Literature DB >> 17971127 |
A S Bienemann1, Y B Lee, J Howarth, J B Uney.
Abstract
The anti-apoptotic effects of heat-shock protein (Hsp70) were assessed in SCG neurones following nerve growth factor (NGF) withdrawal. The results showed that the virally mediated expression of Hsp70 mirrored the effects of the c-Jun-N-terminal kinase (JNK) binding domain (JBD) of JNK interacting protein (an inhibitor of JNK and c-Jun activation) and suppressed the phosphorylation of c-Jun. Preventing c-Jun transcriptional activity subsequently led to reduced cytochrome c release and prevented caspase activation as indicated by a decrease in poly (ADP-ribose) polymerase-1 (PARP) cleavage. Together, these results show that Hsp70 is a highly effective inhibitor of apoptosis in sympathetic neurones and that it mediates this effect primarily by suppressing c-Jun transcriptional signalling.Entities:
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Year: 2007 PMID: 17971127 DOI: 10.1111/j.1471-4159.2007.05006.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372