Hara Makoto R, Thomas Bobby, Cascio Matthew B, Bae Byoung-Il, Hester Lynda D, Dawson Valina L, Dawson Ted M, Sawa Akira, Snyder Solomon H
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3887-9. doi: 10.1073/pnas.0511321103. Epub 2006 Feb 27.
Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) participates in a cell death cascade wherein a variety of stimuli activate nitric oxide (NO) synthases with NO nitrosylating GAPDH, conferring on it the ability to bind to Siah, an E3-ubiquitin-ligase, whose nuclear localization signal enables the GAPDH/Siah protein complex to translocate to the nucleus where degradation of Siah targets elicits cell death. R-(-)-Deprenyl (deprenyl) ameliorates the progression of disability in early Parkinson's disease and also has neuroprotective actions. We show that deprenyl and a related agent, TCH346, in subnanomolar concentrations, prevent S-nitrosylation of GAPDH, the binding of GAPDH to Siah, and nuclear translocation of GAPDH. In mice treated with the dopamine neuronal toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), low doses of deprenyl prevent binding of GAPDH and Siah1 in the dopamine-enriched corpus striatum.
甘油醛-3-磷酸脱氢酶(GAPDH)参与细胞死亡级联反应,其中多种刺激激活一氧化氮(NO)合酶,使NO将GAPDH亚硝基化,赋予其与E3泛素连接酶Siah结合的能力,Siah的核定位信号使GAPDH/Siah蛋白复合物易位至细胞核,在细胞核中Siah靶标的降解引发细胞死亡。R-(-)-司来吉兰(deprenyl)可改善早期帕金森病的残疾进展,且具有神经保护作用。我们发现,司来吉兰及相关药物TCH346在亚纳摩尔浓度下可防止GAPDH的S-亚硝基化、GAPDH与Siah的结合以及GAPDH的核转位。在用多巴胺神经元毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的小鼠中,低剂量的司来吉兰可防止富含多巴胺的纹状体中GAPDH和Siah1的结合。