内质网
未折叠蛋白反应
蛋白质组
蛋白质组学
生物
细胞生物学
转录组
线粒体
分子生物学
基因表达
生物化学
基因
作者
Yen-Yin Tsai,Yi-Huei Huang,Ya-Li Chao,Kuang-Yu Hu,Li‐Te Chin,Shiu-Huey Chou,Ai‐Ling Hour,Yeong-Der Yao,Chi‐Shun Tu,Yao‐Jen Liang,Cheng-Yuh Tsai,Haoyu Wu,Shan-Wen Tan,Han‐Min Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2011-11-22
卷期号:5 (12): 9354-9369
被引量:111
摘要
Growth inhibition and apoptotic/necrotic phenotype was observed in nanogold particle (AuNP)-treated human chronic myelogenous leukemia cells. To elucidate the underlying cellular mechanisms, proteomic techniques including two-dimensional electrophoresis/mass spectrometry and protein microarrays were utilized to study the differentially expressed proteome and phosphoproteome, respectively. Systems biology analysis of the proteomic data revealed that unfolded protein-associated endoplasmic reticulum (ER) stress response was the predominant event. Concomitant with transcriptomic analysis using mRNA expression, microarrays show ER stress response in the AuNP-treated cells. The ER stress protein markers' expression assay unveiled AuNPs as an efficient cellular ER stress elicitor. Upon ER stress, cellular responses, including reactive oxygen species increase, mitochondrial cytochrome c release, and mitochondria damage, chronologically occurred in the AuNP-treated cells. Conclusively, this study demonstrates that AuNPs cause cell death through induction of unmanageable ER stress.
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