Zhang Xiao-fei, Li Chao, Zhao Chang-qi, Liu Li-hong
College of Life Sciences, Beijing Normal University, Beijing 100875, China.
Yao Xue Xue Bao. 2011 May;46(5):513-20.
To investigate whether a series of water-soluble cross-linked chitosan derivates synthesized in the guide of imprinting technology could be used as a uranium chelating agent to protect cells exposed to depleted uranium (DU), the imprinted chitosan derivates with high UO2(2+) chelating ability were screened, and cell model of human renal proximal tubule epithelium cells (HK-2) exposed to DU (500 micromol.L-1) was built, chitosan derivates (400 mg.L-1 ) was added to test group and diethylenetriaminepentaacetic acid (DTPA, 50 mg.L-1) was added to positive control group. The results showed that three Cu2+ imprinted chitosan derivates had higher uranium chelating ability (>49 microg.mg-1) than chitosan and non-imprinted chitosan derivates. Compared to the cells exposed to DU only, survival of cells in group added chitosan derivates rose up significantly (increased from 57.3% to 88.7%, and DTPA to 72.6%), and DU intracellular accumulation decreased, membrane damage and DNA damage also eased. Among the imprinted chitosan derivates, Cu2+ imprinted penta dialdehyde cross-linked carboxymethyl chitosan (Cu-P-CMC) was the best, and better than DTPA. From ultrastructure observation, the DU precipitates of test group added Cu-P-CMC were most grouped in a big hairy clusters in a string together outside cells. It is possible that the DU-chitosan derivates precipitates are too big to enter into cells, and from this way, the DU uptake by cells decreased so as to detoxication.
为研究在印迹技术指导下合成的一系列水溶性交联壳聚糖衍生物是否可作为铀螯合剂来保护暴露于贫铀(DU)的细胞,筛选出具有高UO2(2+)螯合能力的印迹壳聚糖衍生物,构建了暴露于DU(500 μmol·L-1)的人肾近端小管上皮细胞(HK-2)细胞模型,试验组添加壳聚糖衍生物(400 mg·L-1),阳性对照组添加二乙烯三胺五乙酸(DTPA,50 mg·L-1)。结果显示,三种Cu2+印迹壳聚糖衍生物的铀螯合能力(>49 μg·mg-1)高于壳聚糖和非印迹壳聚糖衍生物。与仅暴露于DU的细胞相比,添加壳聚糖衍生物组的细胞存活率显著提高(从57.3%增至88.7%,添加DTPA组增至72.6%),细胞内DU蓄积减少,膜损伤和DNA损伤也减轻。在印迹壳聚糖衍生物中,Cu2+印迹戊二醛交联羧甲基壳聚糖(Cu-P-CMC)效果最佳,且优于DTPA。从超微结构观察,添加Cu-P-CMC的试验组中DU沉淀物大多在细胞外聚集成大的毛簇状。可能是DU-壳聚糖衍生物沉淀物太大无法进入细胞,从而使细胞对DU的摄取减少以实现解毒。