Jacobs S B R, Basak S, Murray J I, Pathak N, Attardi L D
Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305-5152, USA.
Cell Death Differ. 2007 Jul;14(7):1374-85. doi: 10.1038/sj.cdd.4402128. Epub 2007 Apr 20.
p53 plays a central role in neuronal cell death resulting from acute injury or disease. To define the pathway by which p53 triggers apoptosis, we used microarray analysis to identify p53 target genes specifically upregulated during apoptosis but not cell cycle arrest. This analysis identified a small subset of targets highly selective for the p53 apoptotic response, including Siva, a proapoptotic protein whose function is not well understood. Siva's expression pattern suggests that it plays an instructive role in apoptosis, and accordingly, we demonstrate that Siva is essential for p53-dependent apoptosis in cerebellar granule neurons. In addition, we determine that endogenous Siva is associated with the plasma membrane and that Caspase-8 and Bid are important for neuronal apoptosis. Our studies highlight the participation of membrane signaling events in p53's apoptotic program in primary neurons and have significant implications for understanding the mechanisms underlying pathogenesis after neuronal injury and in neurodegenerative diseases.
p53在急性损伤或疾病导致的神经元细胞死亡中起核心作用。为了确定p53触发细胞凋亡的途径,我们使用微阵列分析来鉴定在细胞凋亡而非细胞周期停滞期间特异性上调的p53靶基因。该分析确定了一小部分对p53凋亡反应具有高度选择性的靶标,包括Siva,一种促凋亡蛋白,其功能尚未完全了解。Siva的表达模式表明它在细胞凋亡中起指导作用,因此,我们证明Siva对于小脑颗粒神经元中p53依赖性细胞凋亡至关重要。此外,我们确定内源性Siva与质膜相关,并且半胱天冬酶-8和Bid对神经元细胞凋亡很重要。我们的研究强调了膜信号事件在原代神经元p53凋亡程序中的参与,对于理解神经元损伤后和神经退行性疾病发病机制具有重要意义。