文献类型：期刊文献

中文题名：对乙酰氨基酚耐受肝细胞株的建立及其作用机制研究

英文题名：Establishment of Acetaminophen-Resistant Liver Cell Line and Its Possible Mechanism

作者：曹欢欢[1,2];茅育蕾[1,3];陈娟慧[1];陈佳媛[1];郑锐攀[1];岑梦娇[1];倪坚[1];金立方[1,2]

机构：[1]绍兴文理学院生命科学学院;[2]杭州精准医药研究中心;[3]绍兴文理学院附属医院

年份：2018

卷号：40

期号：5

起止页码：717

中文期刊名：中国细胞生物学学报

外文期刊名：Chinese Journal of Cell Biology

收录：CSTPCD、、CSCD2017_2018、CSCD

基金：浙江省自然科学基金(批准号:Y2110911)资助的课题~~

语种：中文

中文关键词：肝细胞;对乙酰氨基酚;耐药;氧化应激

外文关键词：hepatocytes;acetaminophen;drug resistant;oxidant stress

中文摘要：对乙酰氨基酚(acetaminophen,APAP)是引起急性肝衰竭最主要的原因,但其确切的作用机制仍不明了。该研究建立了不同浓度的APAP耐药肝细胞,并对其耐药机制进行初步研究。克隆状密度培养的AML-12小鼠肝细胞浓度递增诱导建立APAP耐药细胞系;细胞计数检测细胞增殖能力;Mito Tracker和H_2DCF-DA分别检测线粒体膜电位和氧自由基水平;GSH/GSSH检测细胞抗氧化能力;q PCR检测细胞基因表达水平;Western blot检测蛋白质水平。成功建立了增殖和耐药稳定的1.25和2.50 mmol/L APAP耐药AML-12肝细胞。在相应浓度APAP处理后,与对照组相比,耐药组细胞增殖能力强,氧自由基水平低,线粒体膜电位水平高,GSH/GSSH值高。进一步研究结果显示,耐受组细胞抗氧化通路Nrf2及其靶基因表达活性提高,而凋亡相关信号通路JNK及其相关基因活性下降。肝细胞表型特征分析显示,耐药组细胞肝功能相关基因表达水平并未发生显著变化,但与染色体重塑相关的转录因子Foxa1和Foxa2 m RNA和蛋白质水平显著升高。该研究建立了增殖和耐药性状稳定的APAP耐药肝细胞,耐药性状的获得与抗氧化能力和抗凋亡能力的提高相关,并提示染色体重塑相关转录因子也可能参与这一过程,为深入研究耐药机制奠定了基础。

外文摘要：Acetaminophen（APAP） is the most important common cause of acute liver failure; however, the exact mechanism of toxicity of this analgesic drug is not elucidated. In the present study, we generated APAPresistant liver cell line and determined their basic properties. AML-12 mouse hepatocytes were cultured with clonal cell density to generate APAP-resistant cells by means of gradually increasing the concentration of the APAP drug. Cell proliferation was determined by cell counting. The levels of reactive oxygen species（ROS） and mitochondrial membrane potential（MMP） were determined by H2 DCF-DA and Mito Tracker detection, respectively. The levels of m RNA and protein were determined by q PCR and Western blot analysis, respectively. We successfully established 1.25 and 2.50 mmol/L APAP-resistant AML-12 cell lines（ARCs）. Cell proliferation analysis revealed that, compared to the control group, ARCs had high proliferation capacity, low ROS levels, and high MMP and GSH/GSSH levels. Furthermore, Western blot and q PCR analysis showed that the expression level of the Nrf2 signaling pathway was up-regulated, whereas the level of the JNK signaling pathway was down-regulated. In addition, ARCs retained normal hepatocytic phenotypes, except for the high expressions of Foxa1 and Foxa2 genes, which were related to chromatin remodeling. We successfully established APAP-resistant hepatocyte lines with low oxidative stress levels but with retained normal hepatocytic phenotypes. Activation of Nrf2 and inactivation of JNK signaling pathway appeared to be involved in the protection of hepatocytes against APAP-induced cell apoptosis.