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二氧化钛纳米颗粒改变A549细胞中的细胞磷酸化蛋白质组。

Titanium Dioxide Nanoparticles Alter the Cellular Phosphoproteome in A549 Cells.

作者信息

Biola-Clier Mathilde, Gaillard Jean-Charles, Rabilloud Thierry, Armengaud Jean, Carriere Marie

机构信息

Univ. Grenoble-Alpes, IRIG, SyMMES, CIBEST, F-38000 Grenoble, France.

Laboratoire Innovations technologiques pour la Détection et le Diagnostic (Li2D), Service de Pharmacologie et Immunoanalyse (SPI), CEA, INRA, F-30207 Bagnols-sur-Cèze, France.

出版信息

Nanomaterials (Basel). 2020 Jan 21;10(2):185. doi: 10.3390/nano10020185.

Abstract

TiO nanoparticles (NPs) are one of the most produced NPs worldwide and are used in many consumer products. Their impact on human health, especially through inhalation, has been studied for more than two decades. TiO is known for its strong affinity towards phosphates, and consequently interaction with cellular phosphates may be one of the mechanisms driving its toxicity. In the present study, we used a phosphoproteomics approach to document the interaction of TiO-NP with phosphoproteins from A549 human pulmonary alveolar epithelial cells. Cells were exposed to 21 nm anatase/rutile TiO-NPs, then their phosphopeptides were extracted and analyzed using shotgun proteomics. By comparing the phosphoprotein content, phosphorylation status and phosphorylation sites of exposed cells with that of control cells, our results show that by affecting the phosphoproteome, TiO-NPs affect cellular processes such as apoptosis, linked with cell cycle and the DNA damage response, TP53 being central to these pathways. Other pathways including inflammation and molecular transport are also affected. These molecular mechanisms of TiO-NP toxicity have been reported previously, our study shows for the first time that they may derive from phosphoproteome modulation, which could be one of their upstream regulators.

摘要

二氧化钛纳米颗粒(NPs)是全球产量最高的纳米颗粒之一,被用于许多消费品中。二十多年来,人们一直在研究它们对人类健康的影响,尤其是通过吸入途径。二氧化钛以其对磷酸盐的强亲和力而闻名,因此与细胞内磷酸盐的相互作用可能是其毒性作用的机制之一。在本研究中,我们采用磷酸化蛋白质组学方法来记录二氧化钛纳米颗粒与A549人肺泡上皮细胞中磷蛋白的相互作用。将细胞暴露于21纳米的锐钛矿/金红石型二氧化钛纳米颗粒中,然后提取其磷酸肽并使用鸟枪法蛋白质组学进行分析。通过比较暴露细胞与对照细胞的磷蛋白含量、磷酸化状态和磷酸化位点,我们的结果表明,二氧化钛纳米颗粒通过影响磷酸化蛋白质组,影响细胞凋亡等细胞过程,这些过程与细胞周期和DNA损伤反应相关,TP53是这些途径的核心。包括炎症和分子运输在内的其他途径也受到影响。二氧化钛纳米颗粒毒性的这些分子机制此前已有报道,我们的研究首次表明它们可能源于磷酸化蛋白质组的调节,这可能是其上游调节因子之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c60b/7074930/cb0a4ad25dd3/nanomaterials-10-00185-g001.jpg

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