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ABC 转运蛋白在 MPA-COOH-CdTe 量子点在人乳腺癌 SK-BR-3 细胞中的外排和毒性中的作用。

Involvement of ABC transporters in the efflux and toxicity of MPA-COOH-CdTe quantum dots in human breast cancer SK-BR-3 cells.

机构信息

Department of Breast Surgery, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, PR China.

Department of cardiothoracic surgery, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, PR China.

出版信息

J Biochem Mol Toxicol. 2019 Aug;33(8):e22343. doi: 10.1002/jbt.22343. Epub 2019 Apr 20.

Abstract

This paper aimed to study the possible involvement of adenosine triphosphate-binding cassette (ABC) transporters in the detoxification of quantum dots (QDs) in human breast carcinoma (SK-BR-3) cells. The effects of QD sizes on such interactions were also evaluated. For this purpose, we used monodispersed MPA-COOH-CdTe QDs with different diameters (emission length at 560 and 625 nm, named as QD-560 and QD-625). Such QDs tended to accumulate in cells and cause significant toxicity. Using specific inhibitors of ABC transporters, the cellular accumulation and toxicity of QDs in SK-BR-3 cells were significantly affected. Moreover, treatment of QDs caused concentration- and time-dependent induction of ABC transporters. Furthermore, the induction effects of smaller QDs were found to be greater than larger ones at equivalent concentrations, suggesting a size-dependent recognition of substrates by ABC transporters. Overall, these results provided important support for the modulation of QDs toxicity by ABC transporters.

摘要

本文旨在研究三磷酸腺苷结合盒(ABC)转运蛋白是否参与了人乳腺癌(SK-BR-3)细胞中量子点(QD)的解毒过程。同时还评估了 QD 尺寸对这种相互作用的影响。为此,我们使用了具有不同直径(发射长度为 560nm 和 625nm,分别命名为 QD-560 和 QD-625)的单分散 MPA-COOH-CdTe QD。这些 QD 容易在细胞内积累,导致明显的毒性。使用 ABC 转运蛋白的特异性抑制剂,QD 在 SK-BR-3 细胞中的细胞积累和毒性受到显著影响。此外,QD 的处理导致 ABC 转运蛋白的浓度和时间依赖性诱导。此外,在等效浓度下,较小 QD 的诱导作用大于较大 QD,表明 ABC 转运蛋白对底物具有尺寸依赖性识别。总的来说,这些结果为 ABC 转运蛋白调节 QD 毒性提供了重要依据。

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