Effects of Graphene Oxide Nanoparticles on the Immune System Biomarkers Produced by RAW 264.7 and Human Whole Blood Cell Cultures

被引:43
作者
Lategan, Kim [1 ]
Alghadi, Hend [1 ]
Bayati, Mohamed [2 ]
de Cortalezzi, Maria Fidalgo [2 ]
Pool, Edmund [1 ]
机构
[1] Univ Western Cape, Dept Med Biosci, ZA-7535 Cape Town, South Africa
[2] Univ Missouri, Dept Civil & Environm Engn, Columbia, MO 65211 USA
基金
新加坡国家研究基金会;
关键词
graphene oxide nanoparticles; cytotoxicity; macrophage activation; humoral immune response; IN-VITRO; SIGNAL-TRANSDUCTION; INTERFERON-GAMMA; IMMUNOTOXICITY; PATHWAY; HETEROAGGREGATION; NANOMATERIALS; MACROPHAGES; MECHANISMS; NANOSHEETS;
D O I
10.3390/nano8020125
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene oxide nanoparticles (GONPs) have attracted a lot of attention due to their many applications. These applications include batteries, super capacitors, drug delivery and biosensing. However, few studies have investigated the effects of these nanoparticles on the immune system. In this study, the in vitro effects of GONPs on the immune system was evaluated by exposing murine macrophages, RAW 264.7 cells and human whole blood cell cultures (to GONPs. The effects of GONPs on RAW cells were monitored under basal conditions. The whole blood cell cultures were exposed to GONPs in the presence or absence of the mitogens lipopolysaccharide (LPS) and phytohaemmagglutinin (PHA). A number of parameters were monitored for both RAW and whole blood cell cultures, these included cytotoxicity, inflammatory biomarkers, cytokines of the acquired immune system and a proteome profile analysis. The GONPs were cytotoxic to both RAW and whole blood cell cultures at 500 mu g/mL. In the absence of LPS, GONPs elicited an inflammatory response from the murine macrophage, RAW and whole blood cell cultures at 15.6 and 5 mu g/mL respectively. This activation was further corroborated by proteome profile analysis of both experimental cultures. GONPs inhibited LPS induced interleukin 6 (IL-6) synthesis and PHA induced interferon gamma (IFN gamma) synthesis by whole blood cell cultures in a dose dependent manner. In the absence of mitogens, GONPs stimulated IL-10 synthesis by whole blood cell cultures. The current study shows that GONPs modulate immune system biomarkers and that these may pose a health risk to individuals exposed to this type of nanoparticle.
引用
收藏
页数:16
相关论文
共 33 条
[1]   Toxicity of Graphene and Graphene Oxide Nanowalls Against Bacteria [J].
Akhavan, Omid ;
Ghaderi, Elham .
ACS NANO, 2010, 4 (10) :5731-5736
[2]   Oxidative stress and immunotoxicity induced by graphene oxide in zebrafish [J].
Chen, Minjie ;
Yin, Junfa ;
Liang, Yong ;
Yuan, Shaopeng ;
Wang, Fengbang ;
Song, Maoyong ;
Wang, Hailin .
AQUATIC TOXICOLOGY, 2016, 174 :54-60
[3]   Role of toll-like receptors 3, 4 and 7 in cellular uptake and response to titanium dioxide nanoparticles [J].
Chen, Peng ;
Kanehira, Koki ;
Taniguchi, Akiyoshi .
SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS, 2013, 14 (01)
[4]   Graphene/graphene oxide and their derivatives in the separation/isolation and preconcentration of protein species: A review [J].
Chen, Xuwei ;
Hai, Xin ;
Wang, Jianhua .
ANALYTICA CHIMICA ACTA, 2016, 922 :1-10
[5]  
Cherian R. S., 2014, J NANOMED NANOTECHNO, V5, P200
[6]   Colloidal Properties and Stability of Graphene Oxide Nanomaterials in the Aquatic Environment [J].
Chowdhury, Indranil ;
Duch, Matthew C. ;
Mansukhani, Nikhita D. ;
Hersam, Mark C. ;
Bouchard, Dermont .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2013, 47 (12) :6288-6296
[7]   Screening of xenobiotics for direct immunotoxicity in an animal study [J].
De Jong, Wim H. ;
Van Loveren, Henk .
METHODS, 2007, 41 (01) :3-8
[8]   The interleukin-10 signal transduction pathway and regulation of gene expression in mononuclear phagocytes [J].
Donnelly, RP ;
Dickensheets, H ;
Finbloom, DS .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1999, 19 (06) :563-573
[9]  
Elimelech M., 1998, Particle deposition aggregation, measurement, modeling and simulation
[10]   In vitro evaluation of graphene oxide nanosheets on immune function [J].
Feito, M. J. ;
Vila, M. ;
Matesanz, M. C. ;
Linares, J. ;
Goncalves, G. ;
Marques, P. A. A. P. ;
Vallet-Regi, M. ;
Rojo, J. M. ;
Portoles, M. T. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2014, 432 :221-228