Dorier Marie, Béal David, Marie-Desvergne Caroline, Dubosson Muriel, Barreau Frédérick, Houdeau Eric, Herlin-Boime Nathalie, Carriere Marie
a Chimie Interface Biologie pour l'Environnement, la Santé et la Toxicologie (CIBEST) , INAC, SyMMES, University of Grenoble Alpes , Grenoble , France.
b Chimie Interface Biologie pour l'Environnement, la Santé et la Toxicologie (CIBEST) , CEA, INAC, LCIB , Grenoble , France.
Nanotoxicology. 2017 Aug;11(6):751-761. doi: 10.1080/17435390.2017.1349203. Epub 2017 Jul 19.
The whitening and opacifying properties of titanium dioxide (TiO) are commonly exploited when it is used as a food additive (E171). However, the safety of this additive can be questioned as TiO nanoparticles (TiO-NPs) have been classed at potentially toxic. This study aimed to shed some light on the mechanisms behind the potential toxicity of E171 on epithelial intestinal cells, using two in vitro models: (i) a monoculture of differentiated Caco-2 cells and (ii) a coculture of Caco-2 with HT29-MTX mucus-secreting cells. Cells were exposed to E171 and two different types of TiO-NPs, either acutely (6-48 h) or repeatedly (three times a week for 3 weeks). Our results confirm that E171 damaged these cells, and that the main mechanism of toxicity was oxidation effects. Responses of the two models to E171 were similar, with a moderate, but significant, accumulation of reactive oxygen species, and concomitant downregulation of the expression of the antioxidant enzymes catalase, superoxide dismutase and glutathione reductase. Oxidative damage to DNA was detected in exposed cells, proving that E171 effectively induces oxidative stress; however, no endoplasmic reticulum stress was detected. E171 effects were less intense after acute exposure compared to repeated exposure, which correlated with higher Ti accumulation. The effects were also more intense in cells exposed to E171 than in cells exposed to TiO-NPs. Taken together, these data show that E171 induces only moderate toxicity in epithelial intestinal cells, via oxidation.
二氧化钛(TiO)用作食品添加剂(E171)时,其美白和遮光特性常被利用。然而,这种添加剂的安全性可能受到质疑,因为TiO纳米颗粒(TiO-NPs)已被归类为具有潜在毒性。本研究旨在通过两种体外模型,阐明E171对肠道上皮细胞潜在毒性背后的机制:(i)分化的Caco-2细胞单培养物,以及(ii)Caco-2与HT29-MTX黏液分泌细胞的共培养物。细胞急性(6 - 48小时)或反复(每周三次,共3周)暴露于E171和两种不同类型的TiO-NPs。我们的结果证实,E171会损伤这些细胞,且主要毒性机制是氧化作用。两种模型对E171的反应相似,活性氧有中度但显著的积累,同时抗氧化酶过氧化氢酶、超氧化物歧化酶和谷胱甘肽还原酶的表达下调。在暴露的细胞中检测到DNA的氧化损伤,证明E171能有效诱导氧化应激;然而,未检测到内质网应激。与反复暴露相比,急性暴露后E171的影响较小,这与更高的钛积累相关。E171对细胞的影响也比对TiO-NPs暴露的细胞更强烈。综上所述,这些数据表明,E171通过氧化作用仅在上皮肠道细胞中诱导中度毒性。