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八面体铼簇合物的细胞摄取和细胞毒性

Cellular uptake and cytotoxicity of octahedral rhenium cluster complexes.

作者信息

Choi Soo-Jin, Brylev Konstantin A, Xu Jing-Zhe, Mironov Yuri V, Fedorov Vladimir E, Sohn Youn Soo, Kim Sung-Jin, Choy Jin-Ho

机构信息

Division of Nano Sciences BK21, Department of Chemistry and Nano Science, Ewha Womans University, Seoul 120-750, Republic of Korea.

出版信息

J Inorg Biochem. 2008 Nov;102(11):1991-6. doi: 10.1016/j.jinorgbio.2008.07.013. Epub 2008 Aug 3.

Abstract

Cellular uptake behavior of a novel class of octahedral rhenium cluster compounds, hexahydroxo complexes K(4)[{Re(6)S(8)}(OH)(6)].8H(2)O (1) and K(4)[{Re(6)Se(8)}(OH)(6)].8H(2)O (2), was evaluated in human cervical adenocarcinoma HeLa cells. Confocal microscopy and flow cytometry studies demonstrated that rhenium cluster 1 was not internalized into cell, while rhenium cluster 2 was. Conjugation of a polymer to rhenium cluster 1, namely the derivative K(4)[{Re(6)S(8)}(OH)(5)L] (3) (L is amphiphilic diblock copolymer MPEG550-CH(2)CONH-GlyPheLeuGlyPheLeu-COO(-)), considerably enhanced cellular uptake in a concentration-dependent manner and was predominantly localized in the cytoplasm and nucleus upon incubation time. The uptake of rhenium cluster 2 was mediated by energy-dependent endocytosis, whereas rhenium cluster 3 was directly ingested into cells by cell-fusion-like mechanism. According to the cytotoxicity evaluation test, both rhenium clusters 2 and 3 did not exhibit acute cytotoxic effects up to 50 microM, at the practical concentration level of biological applications. It is, therefore, expected that the rhenium cluster complexes can be promising potential candidates as diagnostic agents for medical treatment.

摘要

在人宫颈腺癌HeLa细胞中评估了一类新型八面体铼簇化合物,即六羟基配合物K(4)[{Re(6)S(8)}(OH)(6)].8H(2)O (1)和K(4)[{Re(6)Se(8)}(OH)(6)].8H(2)O (2)的细胞摄取行为。共聚焦显微镜和流式细胞术研究表明,铼簇1未内化到细胞中,而铼簇2则被内化。将一种聚合物与铼簇1偶联,即衍生物K(4)[{Re(6)S(8)}(OH)(5)L] (3)(L为两亲性二嵌段共聚物MPEG550-CH(2)CONH-GlyPheLeuGlyPheLeu-COO(-)),以浓度依赖的方式显著增强了细胞摄取,并且在孵育后主要定位于细胞质和细胞核中。铼簇2的摄取是由能量依赖的内吞作用介导的,而铼簇3是通过类似细胞融合的机制直接摄入细胞的。根据细胞毒性评估试验,在生物应用的实际浓度水平下,铼簇2和3在高达50 microM时均未表现出急性细胞毒性作用。因此,预计铼簇配合物有望成为有前途的潜在医疗诊断剂候选物。

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