Hong Yeon-Mi, Hong Yohan, Choi Yeong-Gon, Yeo Sujung, Jin Soo Hee, Lee Sae-Won, Sung Backil, Lee Sook-Hyun, Jung Hyejin, Lim Sabina
Research Group of Pain and Neuroscience, East-West Medical Research Institute, Kyung Hee University, Seoul, Republic of Korea; Department of Meridian & Acupoint, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea.
Research Group of Pain and Neuroscience, East-West Medical Research Institute, Kyung Hee University, Seoul, Republic of Korea; Department of Neurodegenerative Diseases, Ilsong Institute of Life Science, Hallym University, Anyang, Republic of Korea.
Oxid Med Cell Longev. 2017;2017:7982389. doi: 10.1155/2017/7982389. Epub 2017 Feb 9.
In a previous study, we found that the short isoform of DNAJB6 (DNAJB6(S)) had been decreased in the striatum of a mouse model of Parkinson's disease (PD) induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). DNAJB6, one of the heat shock proteins, has been implicated in the pathogenesis of PD. In this study, we explored the cytoprotective effect of DNAJB6(S) against 1-methyl-4-phenylpyridinium ion- (MPP-) induced apoptosis and the underlying molecular mechanisms in cultured LN18 cells from astrocytic tumors. We observed that MPP significantly reduced the cell viability and induced apoptosis in LN18 glioblastoma cells. DNAJB6(S) protected LN18 cells against MPP-induced apoptosis not only by suppressing Bax cleavage but also by inhibiting a series of apoptotic events including loss of mitochondrial membrane potential, increase in intracellular reactive oxygen species, and activation of caspase-9. These observations suggest that the cytoprotective effects of DNAJB6(S) may be mediated, at least in part, by the mitochondrial pathway of apoptosis.
在先前的一项研究中,我们发现,在1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病(PD)小鼠模型的纹状体中,DNAJB6的短异构体(DNAJB6(S))减少。热休克蛋白之一的DNAJB6与PD的发病机制有关。在本研究中,我们探讨了DNAJB6(S)对1-甲基-4-苯基吡啶离子(MPP⁺)诱导的星形细胞瘤培养的LN18细胞凋亡的细胞保护作用及其潜在分子机制。我们观察到,MPP⁺显著降低了LN18胶质母细胞瘤细胞的活力并诱导其凋亡。DNAJB6(S)保护LN18细胞免受MPP⁺诱导的凋亡,不仅通过抑制Bax裂解,还通过抑制一系列凋亡事件,包括线粒体膜电位丧失、细胞内活性氧增加和caspase-9激活。这些观察结果表明,DNAJB6(S)的细胞保护作用可能至少部分地通过凋亡的线粒体途径介导。