Literature DB >> 26554512

Low levels of graphene and graphene oxide inhibit cellular xenobiotic defense system mediated by efflux transporters.

Su Liu1, Wei Jiang1, Bing Wu1,2, Jing Yu1, Haiyan Yu1, Xu-Xiang Zhang1, Cristina Torres-Duarte2, Gary N Cherr2,3.   

Abstract

Low levels of graphene and graphene oxide (GO) are considered to be environmentally safe. In this study, we analyzed the potential effects of graphene and GO at relatively low concentrations on cellular xenobiotic defense system mediated by efflux transporters. The results showed that graphene (<0.5 μg/mL) and GO (<20 μg/mL) did not decrease cell viability, generate reactive oxygen species, or disrupt mitochondrial function. However, graphene and GO at the nontoxic concentrations could increase calcein-AM (CAM, an indicator of membrane ATP-binding cassette (ABC) transporter) activity) accumulation, indicating inhibition of ABC transporters' efflux capabilities. This inhibition was observed even at 0.005 μg/mL graphene and 0.05 μg/mL GO, which are 100 times and 400 times lower than their lowest toxic concentration from cytotoxicity experiments, respectively. The inhibition of ABC transporters significantly increased the toxicity of paraquat and arsenic, known substrates of ABC transporters. The inhibition of ABC transporters was found to be based on graphene and GO damaging the plasma membrane structure and fluidity, thus altering functions of transmembrane ABC transporters. This study demonstrates that low levels of graphene and GO are not environmentally safe since they can significantly make cell more susceptible to other xenobiotics, and this chemosensitizing activity should be considered in the risk assessment of graphene and GO.

Entities:  

Keywords:  ABC transporter; HepG2; cytotoxicity; graphene; graphene oxide

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Substances:

Year:  2015        PMID: 26554512     DOI: 10.3109/17435390.2015.1104739

Source DB:  PubMed          Journal:  Nanotoxicology        ISSN: 1743-5390            Impact factor:   5.913


  6 in total

1.  Impact of emerging, high-production-volume graphene-based materials on the bioavailability of benzo(a)pyrene to brine shrimp and fish liver cells.

Authors:  April L Rodd; Cintia J Castilho; Carlos Ef Chaparro; J Rene Rangel-Mendez; Robert H Hurt; Agnes B Kane
Journal:  Environ Sci Nano       Date:  2018-07-31

2.  Characteristic synergistic cytotoxic effects toward cells in graphene oxide dressing with cadmium and copper ions.

Authors:  Yiyang Dong; Yulin Chang; Haidi Gao; Victoria Arantza León Anchustegui; Qiang Yu; Haifang Wang; Jia-Hui Liu; Shihui Wang
Journal:  Toxicol Res (Camb)       Date:  2019-09-16       Impact factor: 3.524

3.  Sub-Lethal Concentrations of Graphene Oxide Trigger Acute-Phase Response and Impairment of Phase-I Xenobiotic Metabolism in Upcyte® Hepatocytes.

Authors:  A Romaldini; R Spanò; F Catalano; F Villa; A Poggi; S Sabella
Journal:  Front Bioeng Biotechnol       Date:  2022-05-19

4.  TiO2 nanoparticles potentiated the cytotoxicity, oxidative stress and apoptosis response of cadmium in two different human cells.

Authors:  Maqusood Ahamed; Mohd Javed Akhtar; ZabnAllah M Alaizeri; Hisham A Alhadlaq
Journal:  Environ Sci Pollut Res Int       Date:  2020-01-15       Impact factor: 4.223

5.  Comparative analysis of toxicity reduction of wastewater in twelve industrial park wastewater treatment plants based on battery of toxicity assays.

Authors:  Yue Yu; Bing Wu; Linmiao Jiang; Xu-Xiang Zhang; Hong-Qiang Ren; Mei Li
Journal:  Sci Rep       Date:  2019-03-06       Impact factor: 4.379

6.  Comparison of cytotoxicity and membrane efflux pump inhibition in HepG2 cells induced by single-walled carbon nanotubes with different length and functional groups.

Authors:  Zhuoyan Shen; Jialu Wu; Yue Yu; Su Liu; Wei Jiang; Habiba Nurmamat; Bing Wu
Journal:  Sci Rep       Date:  2019-05-17       Impact factor: 4.379

  6 in total

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