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纳米颗粒中残留的过硫酸铵通过上皮-间充质转化对细胞产生细胞毒性作用。

Residual Ammonium Persulfate in Nanoparticles Has Cytotoxic Effects on Cells through Epithelial-Mesenchymal Transition.

机构信息

Deparment of Anatomy, Guangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, Southern Medical University, Guangdong, Guangzhou, 510515, China.

出版信息

Sci Rep. 2017 Sep 18;7(1):11769. doi: 10.1038/s41598-017-12328-0.

Abstract

Ammonium persulfate (APS), a low molecular weight chemical compound with strong oxidizing properties, should to be totally removed during preparation of nanomaterials due to its cytotoxicity. APS exerts its oxidative stress effects mainly on cell membrane, but its intracellular influence remains unclear. Here, we designed a facile negatively-charged carboxylic gelatin-methyacrylate (carbox-GelMA) nanoparticle (NP) as a cargo-carrier through the catalytic and oxidizing action of APS in W/O system. The formed APS-loaded carbox-GelMA NPs (APS/NPs) were transported into the lysosome in MCF-7 breast cancer cells. The intracellular APS/NPs produced a high level of oxidative stress in lysosome and induced epithelial-mesenchymal transition (EMT). Consequently, the MCF-7 cells challenged with APS/NPs had a strong metastatic and invasive capability in vitro and in vivo. This study highlights that a facile APS-loaded nanocarrier has cyctotoxicity on cells through EMT. Unexpectedly, we found a novel pathway inducing EMT via lysosomal oxidative stress.

摘要

过硫酸铵(APS)是一种具有强氧化性的低分子量化学物质,由于其细胞毒性,在制备纳米材料时应完全去除。APS 主要通过细胞膜发挥其氧化应激作用,但细胞内的影响尚不清楚。在这里,我们设计了一种简便的带负电荷的羧酸明胶-甲基丙烯酰胺(carbox-GelMA)纳米颗粒(NP),通过 W/O 体系中 APS 的催化和氧化作用作为载体。形成的载有 APS 的羧酸明胶-甲基丙烯酰胺 NPs(APS/NPs)被运送到 MCF-7 乳腺癌细胞的溶酶体中。细胞内的 APS/NPs 在溶酶体中产生高水平的氧化应激,并诱导上皮-间充质转化(EMT)。因此,用 APS/NPs 处理的 MCF-7 细胞在体外和体内具有很强的转移和侵袭能力。这项研究强调,一种简便的载有 APS 的纳米载体通过 EMT 对细胞具有细胞毒性。出乎意料的是,我们发现了一种通过溶酶体氧化应激诱导 EMT 的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/5603593/4961d7fcbb65/41598_2017_12328_Fig1_HTML.jpg

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