Huang Zhenhua, Tong Yufeng, Wang Jinfeng, Huang Youguo
National Laboratory of Biomacromolecules, Center for Molecular Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.
Cancer Cell Int. 2003 Apr 8;3(1):5. doi: 10.1186/1475-2867-3-5.
Changes of membrane lipids in cisplatin-sensitive A549 and cisplatin-resistant A549/DDP cells during the apoptotic process induced by a clinical dose of cisplatin (30 &mgr;M) were detected by 1H and 31P-NMR spectroscopy and by membrane fluidity measurement. The apoptotic phenotypes of the two cell lines were monitored with flow cytometry. The assays of apoptosis showed that significant apoptotic characteristics of the A549 cells were induced when the cells were cultured for 24 hours after treatment with cisplatin, while no apoptotic characteristic could be detected for the resistant A549/DDP cells even after 48 hours. The results of 1H-NMR spectroscopy demonstrated that the CH2/CH3 and Glu/Ct ratios of the membrane of A549 cells increased significantly, but those in A549/DDP cell membranes decreased. In addition, the Chol/CH3 and Eth/Ct ratios decreased for the former but increased for the latter cells under the same conditions. 31P-NMR spectroscopy indicated levels of phosphomonoesters (PME) and ATP decreased in A549 but increased in A549/DDP cells after being treated with cisplatin. These results were supported with the data obtained from 1H-NMR measurements. The results clearly indicated that components and properties of membrane phospholipids of the two cell lines were significantly different during the apoptotic process when they were treated with a clinical dose of cisplatin. Plasma membrane fluidity changes during cisplatin treatment as detected with the fluorescence probe TMA-DPH also indicate marked difference between the two cell lines. We provided evidence that there are significant differences in plasma membrane changes during treatment of cisplatin sensitive A549 and resistant A549/DDP cells.
采用1H和31P核磁共振波谱法以及膜流动性测量方法,检测临床剂量顺铂(30μM)诱导凋亡过程中,顺铂敏感型A549细胞和顺铂耐药型A549/DDP细胞的膜脂变化。通过流式细胞术监测这两种细胞系的凋亡表型。凋亡检测结果显示,顺铂处理后培养24小时,A549细胞诱导出明显的凋亡特征,而耐药的A549/DDP细胞即使在48小时后也未检测到凋亡特征。1H核磁共振波谱结果表明,A549细胞膜的CH2/CH3和Glu/Ct比值显著增加,而A549/DDP细胞膜的这两个比值则下降。此外,相同条件下,前者的Chol/CH3和Eth/Ct比值下降,而后者细胞的这两个比值升高。31P核磁共振波谱表明,顺铂处理后,A549细胞中的磷酸单酯(PME)和ATP水平下降,而A549/DDP细胞中的这两个水平升高。这些结果得到了1H核磁共振测量数据的支持。结果清楚地表明,临床剂量顺铂处理后,两种细胞系在凋亡过程中膜磷脂的成分和性质存在显著差异。用荧光探针TMA-DPH检测顺铂处理过程中的质膜流动性变化,也表明两种细胞系之间存在明显差异。我们提供的证据表明,顺铂敏感型A549细胞和顺铂耐药型A549/DDP细胞在顺铂处理过程中质膜变化存在显著差异。