• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Mesoporous carbon nanomaterials induced pulmonary surfactant inhibition, cytotoxicity, inflammation and lung fibrosis.

作者信息

Chen Yunan, Yang Yi, Xu Bolong, Wang Shunhao, Li Bin, Ma Juan, Gao Jie, Zuo Yi Y, Liu Sijin

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China.

Department of Mechanical Engineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA.

出版信息

J Environ Sci (China). 2017 Dec;62:100-114. doi: 10.1016/j.jes.2017.08.018. Epub 2017 Sep 8.

DOI:10.1016/j.jes.2017.08.018
PMID:29289281
Abstract

Environmental exposure and health risk upon engineered nanomaterials are increasingly concerned. The family of mesoporous carbon nanomaterials (MCNs) is a rising star in nanotechnology for multidisciplinary research with versatile applications in electronics, energy and gas storage, and biomedicine. Meanwhile, there is mounting concern on their environmental health risks due to the growing production and usage of MCNs. The lung is the primary site for particle invasion under environmental exposure to nanomaterials. Here, we studied the comprehensive toxicological profile of MCNs in the lung under the scenario of moderate environmental exposure. It was found that at a low concentration of 10μg/mL MCNs induced biophysical inhibition of natural pulmonary surfactant. Moreover, MCNs at similar concentrations reduced viability of J774A.1 macrophages and lung epithelial A549 cells. Incubating with nature pulmonary surfactant effectively reduced the cytotoxicity of MCNs. Regarding the pro-inflammatory responses, MCNs activated macrophages in vitro, and stimulated lung inflammation in mice after inhalation exposure, associated with lung fibrosis. Moreover, we found that the size of MCNs played a significant role in regulating cytotoxicity and pro-inflammatory potential of this nanomaterial. In general, larger MCNs induced more pronounced cytotoxic and pro-inflammatory effects than their smaller counterparts. Our results provided valuable information on the toxicological profile and environmental health risks of MCNs, and suggested that fine-tuning the size of MCNs could be a practical precautionary design strategy to increase safety and biocompatibility of this nanomaterial.

摘要

相似文献

1
Mesoporous carbon nanomaterials induced pulmonary surfactant inhibition, cytotoxicity, inflammation and lung fibrosis.
J Environ Sci (China). 2017 Dec;62:100-114. doi: 10.1016/j.jes.2017.08.018. Epub 2017 Sep 8.
2
Analysis of pulmonary surfactant in rat lungs after inhalation of nanomaterials: Fullerenes, nickel oxide and multi-walled carbon nanotubes.吸入纳米材料(富勒烯、氧化镍和多壁碳纳米管)后大鼠肺中肺表面活性物质的分析
Nanotoxicology. 2016;10(2):194-203. doi: 10.3109/17435390.2015.1039093. Epub 2015 May 7.
3
Engineered nanoparticle respiratory exposure and potential risks for cardiovascular toxicity: predictive tests and biomarkers.工程纳米颗粒呼吸暴露与心血管毒性的潜在风险:预测性测试和生物标志物。
Inhal Toxicol. 2009 Jul;21 Suppl 1:68-73. doi: 10.1080/08958370902942566.
4
Lung deposition and toxicological responses evoked by multi-walled carbon nanotubes dispersed in a synthetic lung surfactant in the mouse.多壁碳纳米管在合成肺表面活性剂中的分散对小鼠肺部沉积和毒理学反应的影响。
Arch Toxicol. 2012 Jan;86(1):137-49. doi: 10.1007/s00204-011-0741-y. Epub 2011 Jul 30.
5
Inhalation toxicity assessment of carbon-based nanoparticles.碳基纳米粒子吸入毒性评估。
Acc Chem Res. 2013 Mar 19;46(3):770-81. doi: 10.1021/ar200311b. Epub 2012 May 11.
6
[Pulmonary toxicity of manufactured nanomaterials].[人造纳米材料的肺毒性]
Nihon Eiseigaku Zasshi. 2012 May;67(3):396-400. doi: 10.1265/jjh.67.396.
7
Evaluation of pulmonary and systemic toxicity following lung exposure to graphite nanoplates: a member of the graphene-based nanomaterial family.肺部暴露于石墨纳米片(一种基于石墨烯的纳米材料家族成员)后肺毒性和全身毒性的评估。
Part Fibre Toxicol. 2016 Jun 21;13(1):34. doi: 10.1186/s12989-016-0145-5.
8
Atomic layer deposition coating of carbon nanotubes with zinc oxide causes acute phase immune responses in human monocytes in vitro and in mice after pulmonary exposure.用氧化锌对碳纳米管进行原子层沉积涂层处理,在体外可引起人单核细胞的急性期免疫反应,在肺部暴露后的小鼠体内也会引发这种反应。
Part Fibre Toxicol. 2016 Jun 8;13(1):29. doi: 10.1186/s12989-016-0141-9.
9
SWCNT suppress inflammatory mediator responses in human lung epithelium in vitro.单壁碳纳米管在体外抑制人肺上皮细胞中的炎症介质反应。
Toxicol Appl Pharmacol. 2009 Feb 1;234(3):378-90. doi: 10.1016/j.taap.2008.10.015. Epub 2008 Nov 7.
10
Multi-walled carbon nanotubes directly induce epithelial-mesenchymal transition in human bronchial epithelial cells via the TGF-β-mediated Akt/GSK-3β/SNAIL-1 signalling pathway.多壁碳纳米管通过TGF-β介导的Akt/GSK-3β/SNAIL-1信号通路直接诱导人支气管上皮细胞发生上皮-间质转化。
Part Fibre Toxicol. 2016 Jun 1;13(1):27. doi: 10.1186/s12989-016-0138-4.

引用本文的文献

1
Carbon Nanotube Immunotoxicity in Alveolar Epithelial Type II Cells Is Mediated by Physical Contact-Independent Cell-Cell Interaction with Macrophages as Demonstrated in an Optimized Air-Liquid Interface (ALI) Coculture Model.在优化的气液界面(ALI)共培养模型中证实,肺泡II型上皮细胞中的碳纳米管免疫毒性是通过与巨噬细胞的非物理接触依赖性细胞间相互作用介导的。
Nanomaterials (Basel). 2024 Jul 29;14(15):1273. doi: 10.3390/nano14151273.
2
Nanostructured Medical Devices: Regulatory Perspective and Current Applications.纳米结构医疗设备:监管视角与当前应用
Materials (Basel). 2024 Apr 12;17(8):1787. doi: 10.3390/ma17081787.
3
Lung inflammation perturbation by engineered nanoparticles.
工程纳米颗粒对肺部炎症的干扰
Front Bioeng Biotechnol. 2023 May 25;11:1199230. doi: 10.3389/fbioe.2023.1199230. eCollection 2023.
4
Lung surfactant as a biophysical assay for inhalation toxicology.肺表面活性剂作为吸入毒理学的生物物理检测方法。
Curr Res Toxicol. 2022 Dec 23;4:100101. doi: 10.1016/j.crtox.2022.100101. eCollection 2023.
5
Immunotoxicity of nanomaterials in health and disease: Current challenges and emerging approaches for identifying immune modifiers in susceptible populations.纳米材料在健康和疾病中的免疫毒性:鉴定易感人群中免疫调节剂的当前挑战和新兴方法。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2022 Nov;14(6):e1804. doi: 10.1002/wnan.1804.
6
The emergence of nanoporous materials in lung cancer therapy.纳米多孔材料在肺癌治疗中的出现。
Sci Technol Adv Mater. 2022 Jul 20;23(1):225-274. doi: 10.1080/14686996.2022.2052181. eCollection 2022.
7
Mechanisms of cell injury induced by inhaled molybdenum trioxide nanoparticles in Golden Syrian Hamsters.吸入三氧化钼纳米颗粒引起金黄地鼠细胞损伤的机制。
Exp Biol Med (Maywood). 2022 Dec;247(23):2067-2080. doi: 10.1177/15353702221104033. Epub 2022 Jun 25.
8
An adverse outcome pathway for lung surfactant function inhibition leading to decreased lung function.一条导致肺功能下降的肺表面活性物质功能抑制的不良结局途径。
Curr Res Toxicol. 2021 May 27;2:225-236. doi: 10.1016/j.crtox.2021.05.005. eCollection 2021.
9
Co-culture of human alveolar epithelial (A549) and macrophage (THP-1) cells to study the potential toxicity of ambient PM: a comparison of growth under ALI and submerged conditions.共培养人肺泡上皮(A549)细胞和巨噬细胞(THP-1)以研究环境细颗粒物的潜在毒性:气液界面(ALI)和浸没条件下生长情况的比较
Toxicol Res (Camb). 2020 Sep 24;9(5):636-651. doi: 10.1093/toxres/tfaa072. eCollection 2020 Sep.
10
Interactions of particulate matter and pulmonary surfactant: Implications for human health.颗粒物与肺表面活性剂的相互作用:对人类健康的影响。
Adv Colloid Interface Sci. 2020 Oct;284:102244. doi: 10.1016/j.cis.2020.102244. Epub 2020 Aug 19.