Wang Hua-Qin, Imai Yuzuru, Kataoka Ayane, Takahashi Ryosuke
Department of Neurology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Antioxid Redox Signal. 2007 May;9(5):533-42. doi: 10.1089/ars.2006.1522.
Parkin is the gene responsible for a familial form of Parkinson's disease (PD) termed autosomal recessive juvenile parkinsonism (AR-JP)/PARK2. Parkin has been shown to protect cells from endoplasmic reticulum (ER) stress and oxidative stress, presumably due to its ubiquitin ligase (E3) activity that targets proteins for proteasomal degradation. Although the authors showed that parkin is upregulated in response to ER stress, subsequent reports suggest that it does not represent a universal unfolded protein response (UPR). Here the authors report different regulation of parkin in response to ER stress in different cell lines, demonstrating upregulation of parkin as a cell type-specific response to ER stress. 2-Mercaptoethanol (2-ME) and tunicamycin increased the expression of parkin in SH-SY5Y (H) cells, Neuro2a cells, Goto-P3 cells, but not in SH-SY5Y (J) cells and IMR32 cells. In parallel with these studies, similar upregulation of the parkin coregulated gene (PACRG)/gene adjacent to parkin (Glup) was also observed by ER stress. Luciferase assays failed to detect the transcriptional activation of 500 bp parkin/Glup promoter in response to ER stress. These results indicate that induction of parkin by ER stress represents a cell type-specific response.
帕金蛋白是一种与家族性帕金森病(PD)相关的基因,这种帕金森病被称为常染色体隐性青少年帕金森综合征(AR-JP)/PARK2。帕金蛋白已被证明能保护细胞免受内质网(ER)应激和氧化应激,推测这是由于其泛素连接酶(E3)活性将蛋白质靶向蛋白酶体降解。尽管作者表明帕金蛋白在ER应激反应中上调,但随后的报道表明它并不代表普遍的未折叠蛋白反应(UPR)。在此,作者报道了帕金蛋白在不同细胞系中对ER应激的不同调节,证明帕金蛋白的上调是对ER应激的一种细胞类型特异性反应。2-巯基乙醇(2-ME)和衣霉素可增加SH-SY5Y(H)细胞、Neuro2a细胞、Goto-P3细胞中帕金蛋白的表达,但在SH-SY5Y(J)细胞和IMR32细胞中则不然。与这些研究同时进行的是,ER应激也观察到了帕金蛋白共调节基因(PACRG)/帕金蛋白相邻基因(Glup)的类似上调。荧光素酶检测未能检测到500 bp帕金蛋白/Glup启动子对ER应激的转录激活。这些结果表明,ER应激诱导帕金蛋白是一种细胞类型特异性反应。