• 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

二氧化钛颗粒类型和浓度影响Caco-2细胞中的炎症反应。

Titanium Dioxide Particle Type and Concentration Influence the Inflammatory Response in Caco-2 Cells.

作者信息

Tada-Oikawa Saeko, Ichihara Gaku, Fukatsu Hitomi, Shimanuki Yuka, Tanaka Natsuki, Watanabe Eri, Suzuki Yuka, Murakami Masahiko, Izuoka Kiyora, Chang Jie, Wu Wenting, Yamada Yoshiji, Ichihara Sahoko

机构信息

Department of Human Nutrition, School of Life Studies, Sugiyama Jogakuen University, Nagoya 464-8662, Japan.

Graduate School of Regional Innovation Studies, Mie University, Tsu 514-8507, Japan.

出版信息

Int J Mol Sci. 2016 Apr 16;17(4):576. doi: 10.3390/ijms17040576.

DOI:10.3390/ijms17040576
PMID:27092499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4849032/
Abstract

Titanium dioxide (TiO₂) nanoparticles are widely used in cosmetics, sunscreens, biomedicine, and food products. When used as a food additive, TiO₂ nanoparticles are used in significant amounts as white food-coloring agents. However, the effects of TiO₂ nanoparticles on the gastrointestinal tract remain unclear. The present study was designed to determine the effects of five TiO₂ particles of different crystal structures and sizes in human epithelial colorectal adenocarcinoma (Caco-2) cells and THP-1 monocyte-derived macrophages. Twenty-four-hour exposure to anatase (primary particle size: 50 and 100 nm) and rutile (50 nm) TiO₂ particles reduced cellular viability in a dose-dependent manner in THP-1 macrophages, but in not Caco-2 cells. However, 72-h exposure of Caco-2 cells to anatase (50 nm) TiO₂ particles reduced cellular viability in a dose-dependent manner. The highest dose (50 µg/mL) of anatase (100 nm), rutile (50 nm), and P25 TiO₂ particles also reduced cellular viability in Caco-2 cells. The production of reactive oxygen species tended to increase in both types of cells, irrespective of the type of TiO₂ particle. Exposure of THP-1 macrophages to 50 µg/mL of anatase (50 nm) TiO₂ particles increased interleukin (IL)-1β expression level, and exposure of Caco-2 cells to 50 µg/mL of anatase (50 nm) TiO₂ particles also increased IL-8 expression. The results indicated that anatase TiO₂ nanoparticles induced inflammatory responses compared with other TiO₂ particles. Further studies are required to determine the in vivo relevance of these findings to avoid the hazards of ingested particles.

摘要

二氧化钛(TiO₂)纳米颗粒广泛应用于化妆品、防晒霜、生物医学和食品中。当用作食品添加剂时,TiO₂纳米颗粒被大量用作白色食品着色剂。然而,TiO₂纳米颗粒对胃肠道的影响仍不清楚。本研究旨在确定五种不同晶体结构和尺寸的TiO₂颗粒对人上皮结直肠癌(Caco-2)细胞和THP-1单核细胞衍生巨噬细胞的影响。在THP-1巨噬细胞中,24小时暴露于锐钛矿型(初级粒径:50和100 nm)和金红石型(50 nm)TiO₂颗粒会以剂量依赖的方式降低细胞活力,但在Caco-2细胞中则不会。然而,Caco-2细胞暴露于锐钛矿型(50 nm)TiO₂颗粒72小时会以剂量依赖的方式降低细胞活力。锐钛矿型(100 nm)、金红石型(50 nm)和P25 TiO₂颗粒的最高剂量(50 µg/mL)也会降低Caco-2细胞的活力。无论TiO₂颗粒的类型如何,两种细胞中的活性氧生成均有增加的趋势。将THP-1巨噬细胞暴露于50 µg/mL的锐钛矿型(50 nm)TiO₂颗粒会增加白细胞介素(IL)-1β的表达水平,将Caco-2细胞暴露于50 µg/mL的锐钛矿型(50 nm)TiO₂颗粒也会增加IL-8的表达。结果表明,与其他TiO₂颗粒相比,锐钛矿型TiO₂纳米颗粒会引发炎症反应。需要进一步研究以确定这些发现与体内情况的相关性,以避免摄入颗粒的危害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/3681471ab0e1/ijms-17-00576-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/0f4a68c9a9a5/ijms-17-00576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/4192c93b5877/ijms-17-00576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/f129df80255f/ijms-17-00576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/a96a2c5ad64d/ijms-17-00576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/f8114ce8837c/ijms-17-00576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/7422e47d9cb1/ijms-17-00576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/3681471ab0e1/ijms-17-00576-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/0f4a68c9a9a5/ijms-17-00576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/4192c93b5877/ijms-17-00576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/f129df80255f/ijms-17-00576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/a96a2c5ad64d/ijms-17-00576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/f8114ce8837c/ijms-17-00576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/7422e47d9cb1/ijms-17-00576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b1a/4849032/3681471ab0e1/ijms-17-00576-g007.jpg

相似文献

1
Titanium Dioxide Particle Type and Concentration Influence the Inflammatory Response in Caco-2 Cells.二氧化钛颗粒类型和浓度影响Caco-2细胞中的炎症反应。
Int J Mol Sci. 2016 Apr 16;17(4):576. doi: 10.3390/ijms17040576.
2
In vitro phototoxicity and hazard identification of nano-scale titanium dioxide.纳米二氧化钛的体外光毒性和危害识别。
Toxicol Appl Pharmacol. 2012 Jan 15;258(2):226-36. doi: 10.1016/j.taap.2011.10.023. Epub 2011 Nov 15.
3
The crystal structure of titanium dioxide nanoparticles influences immune activity in vitro and in vivo.二氧化钛纳米颗粒的晶体结构影响体外和体内的免疫活性。
Part Fibre Toxicol. 2018 Jan 30;15(1):9. doi: 10.1186/s12989-018-0245-5.
4
In vitro intestinal epithelium responses to titanium dioxide nanoparticles.体外肠道上皮细胞对二氧化钛纳米颗粒的反应。
Food Res Int. 2019 May;119:634-642. doi: 10.1016/j.foodres.2018.10.041. Epub 2018 Oct 12.
5
Cytotoxicity and genotoxicity of nanosized and microsized titanium dioxide and iron oxide particles in Syrian hamster embryo cells.纳米级和微米级二氧化钛及氧化铁颗粒对叙利亚仓鼠胚胎细胞的细胞毒性和遗传毒性
Ann Occup Hyg. 2012 Jul;56(5):631-44. doi: 10.1093/annhyg/mes006. Epub 2012 Mar 26.
6
Involvement of JNK and P53 activation in G2/M cell cycle arrest and apoptosis induced by titanium dioxide nanoparticles in neuron cells.在神经细胞中,二氧化钛纳米颗粒诱导的 G2/M 细胞周期阻滞和细胞凋亡涉及 JNK 和 P53 的激活。
Toxicol Lett. 2010 Dec 15;199(3):269-76. doi: 10.1016/j.toxlet.2010.09.009. Epub 2010 Sep 21.
7
Titanium dioxide induces different levels of IL-1beta production dependent on its particle characteristics through caspase-1 activation mediated by reactive oxygen species and cathepsin B.二氧化钛通过活性氧和组织蛋白酶 B 介导的半胱天冬酶-1 激活,根据其颗粒特性诱导不同水平的白细胞介素-1β产生。
Biochem Biophys Res Commun. 2010 Feb 5;392(2):160-5. doi: 10.1016/j.bbrc.2009.12.178. Epub 2010 Jan 7.
8
Distinctive toxicity of TiO2 rutile/anatase mixed phase nanoparticles on Caco-2 cells.锐钛矿/金红石混合相二氧化钛纳米颗粒对 Caco-2 细胞的独特毒性。
Chem Res Toxicol. 2012 Mar 19;25(3):646-55. doi: 10.1021/tx200334k. Epub 2012 Feb 10.
9
Cellular responses by stable and uniform ultrafine titanium dioxide particles in culture-medium dispersions when secondary particle size was 100 nm or less.当二次粒径为 100nm 或以下时,在培养基分散体中稳定且均匀的超细二氧化钛颗粒引起的细胞反应。
Toxicol In Vitro. 2010 Sep;24(6):1629-38. doi: 10.1016/j.tiv.2010.06.003. Epub 2010 Jun 10.
10
Food grade titanium dioxide disrupts intestinal brush border microvilli in vitro independent of sedimentation.食品级二氧化钛可在体外独立于沉降作用破坏肠道刷状缘微绒毛。
Cell Biol Toxicol. 2014 Jun;30(3):169-88. doi: 10.1007/s10565-014-9278-1. Epub 2014 May 11.

引用本文的文献

1
Bioaccessibility and cellular transport study of silver and titanium dioxide nanoparticles from exposed seaweed and mussels using Caco-2 cells.利用Caco-2细胞对暴露于海藻和贻贝中的银和二氧化钛纳米颗粒进行生物可及性和细胞转运研究。
Mikrochim Acta. 2025 Mar 8;192(4):216. doi: 10.1007/s00604-025-07066-4.
2
Easy and green synthesis of nano-ZnO and nano-TiO for efficient photocatalytic degradation of organic pollutants.用于高效光催化降解有机污染物的纳米氧化锌和纳米二氧化钛的简便绿色合成方法。
Heliyon. 2024 Sep 5;10(17):e37469. doi: 10.1016/j.heliyon.2024.e37469. eCollection 2024 Sep 15.
3
Emerging strategies for combating in colorectal cancer treatment: Systematic review, improvements and future challenges.

本文引用的文献

1
Zn(II) released from zinc oxide nano/micro particles suppresses vasculogenesis in human endothelial colony-forming cells.从氧化锌纳米/微粒中释放出的锌离子(II)抑制人内皮祖细胞中的血管生成。
Toxicol Rep. 2015 May 2;2:692-701. doi: 10.1016/j.toxrep.2015.04.003. eCollection 2015.
2
Biological effect of food additive titanium dioxide nanoparticles on intestine: an in vitro study.食品添加剂二氧化钛纳米颗粒对肠道的生物学效应:一项体外研究
J Appl Toxicol. 2015 Oct;35(10):1169-78. doi: 10.1002/jat.3171. Epub 2015 Jun 23.
3
Different mechanisms are involved in oxidative DNA damage and genotoxicity induction by ZnO and TiO2 nanoparticles in human colon carcinoma cells.
结直肠癌治疗中新兴的对抗策略:系统综述、进展与未来挑战
Exploration (Beijing). 2023 Dec 22;4(1):20230092. doi: 10.1002/EXP.20230092. eCollection 2024 Feb.
4
Oral intake of titanium dioxide nanoparticles affect the course and prognosis of ulcerative colitis in mice: involvement of the ROS-TXNIP-NLRP3 inflammasome pathway.口服二氧化钛纳米颗粒影响小鼠溃疡性结肠炎的病程和预后:涉及 ROS-TXNIP-NLRP3 炎性体途径。
Part Fibre Toxicol. 2023 Jun 22;20(1):24. doi: 10.1186/s12989-023-00535-9.
5
MRC-5 Human Lung Fibroblasts Alleviate the Genotoxic Effect of Fe-N Co-Doped Titanium Dioxide Nanoparticles through an OGG1/2-Dependent Reparatory Mechanism.MRC-5 人肺成纤维细胞通过 OGG1/2 依赖性修复机制缓解 Fe-N 共掺杂二氧化钛纳米颗粒的遗传毒性作用。
Int J Mol Sci. 2023 Mar 29;24(7):6401. doi: 10.3390/ijms24076401.
6
Adverse Outcome Pathways Associated with the Ingestion of Titanium Dioxide Nanoparticles-A Systematic Review.与摄入二氧化钛纳米颗粒相关的不良结局途径——一项系统综述
Nanomaterials (Basel). 2022 Sep 21;12(19):3275. doi: 10.3390/nano12193275.
7
The impact of selected food additives on the gastrointestinal tract in the example of nonspecific inflammatory bowel diseases.以非特异性炎症性肠病为例,某些食品添加剂对胃肠道的影响。
Arch Med Sci. 2021 Jan 8;18(5):1286-1296. doi: 10.5114/aoms/125001. eCollection 2022.
8
Chronic effects of two rutile TiO nanomaterials in human intestinal and hepatic cell lines.两种锐钛矿 TiO2 纳米材料对人肠道和肝脏细胞系的慢性影响。
Part Fibre Toxicol. 2022 May 17;19(1):37. doi: 10.1186/s12989-022-00470-1.
9
Investigating the Molecular Processes behind the Cell-Specific Toxicity Response to Titanium Dioxide Nanobelts.研究钛纳米带细胞特异性毒性反应背后的分子过程。
Int J Mol Sci. 2021 Aug 30;22(17):9432. doi: 10.3390/ijms22179432.
10
TiO - do we have to worry about it? One of the important aetiological factors in inflammatory bowel disease.二氧化钛——我们需要担心它吗?它是炎症性肠病的重要病因之一。
Prz Gastroenterol. 2021;6(2):106-110. doi: 10.5114/pg.2021.106660. Epub 2021 Jun 4.
氧化锌和二氧化钛纳米颗粒在人结肠癌细胞中诱导氧化DNA损伤和遗传毒性的机制不同。
Toxicol In Vitro. 2015 Oct;29(7):1503-12. doi: 10.1016/j.tiv.2015.06.009. Epub 2015 Jun 13.
4
Synergistic effect of bolus exposure to zinc oxide nanoparticles on bleomycin-induced secretion of pro-fibrotic cytokines without lasting fibrotic changes in murine lungs.一次性暴露于氧化锌纳米颗粒对博来霉素诱导的促纤维化细胞因子分泌的协同作用,且小鼠肺部无持久性纤维化改变。
Int J Mol Sci. 2014 Dec 30;16(1):660-76. doi: 10.3390/ijms16010660.
5
Tissue distribution and elimination after oral and intravenous administration of different titanium dioxide nanoparticles in rats.大鼠口服和静脉注射不同二氧化钛纳米颗粒后的组织分布与消除
Part Fibre Toxicol. 2014 Jul 3;11:30. doi: 10.1186/1743-8977-11-30.
6
Proinflammatory effects of diesel exhaust nanoparticles on scleroderma skin cells.柴油废气纳米颗粒对硬皮病皮肤细胞的促炎作用。
J Immunol Res. 2014;2014:138751. doi: 10.1155/2014/138751. Epub 2014 Jun 1.
7
Titanium dioxide nanoparticles induce strong oxidative stress and mitochondrial damage in glial cells.二氧化钛纳米颗粒在神经胶质细胞中诱导强烈的氧化应激和线粒体损伤。
Free Radic Biol Med. 2014 Aug;73:84-94. doi: 10.1016/j.freeradbiomed.2014.04.026. Epub 2014 May 10.
8
Cell uptake and oral absorption of titanium dioxide nanoparticles.纳米二氧化钛的细胞摄取和口服吸收。
Toxicol Lett. 2014 Jul 15;228(2):103-10. doi: 10.1016/j.toxlet.2014.04.014. Epub 2014 May 1.
9
Zinc oxide nanoparticles induce migration and adhesion of monocytes to endothelial cells and accelerate foam cell formation.氧化锌纳米颗粒诱导单核细胞迁移和黏附在内皮细胞上,并加速泡沫细胞的形成。
Toxicol Appl Pharmacol. 2014 Jul 1;278(1):16-25. doi: 10.1016/j.taap.2014.04.010. Epub 2014 Apr 16.
10
Titanium dioxide nanoparticle impact and translocation through ex vivo, in vivo and in vitro gut epithelia.二氧化钛纳米颗粒对离体、体内和体外肠道上皮的影响及转运
Part Fibre Toxicol. 2014 Mar 25;11:13. doi: 10.1186/1743-8977-11-13.