Bienemann A S, Lee Y B, Howarth J, Uney J B
Henry Wellcome Laboratories for Integrated Neuroscience and Endocrinology, University of Bristol, Bristol, UK.
J Neurochem. 2008 Jan;104(1):271-8. doi: 10.1111/j.1471-4159.2007.05006.x. Epub 2007 Oct 30.
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.
在撤除神经生长因子(NGF)后,对颈上神经节(SCG)神经元中热休克蛋白(Hsp70)的抗凋亡作用进行了评估。结果显示,病毒介导的Hsp70表达反映了JNK相互作用蛋白(一种JNK和c-Jun激活的抑制剂)的c-Jun氨基末端激酶(JNK)结合结构域(JBD)的作用,并抑制了c-Jun的磷酸化。如聚(ADP-核糖)聚合酶-1(PARP)裂解减少所示,阻止c-Jun转录活性随后导致细胞色素c释放减少并阻止了半胱天冬酶激活。总之,这些结果表明,Hsp70是交感神经元中一种高效的凋亡抑制剂,并且它主要通过抑制c-Jun转录信号传导来介导这种作用。