• 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

使用酿酒酵母作为模式生物评估单壁碳纳米管的生物相容性。

Biocompatibility assessment of single-walled carbon nanotubes using Saccharomyces cerevisiae as a model organism.

机构信息

College of Animal Science and Technology, Northwest A&F University, Xinong Road 22nd, Yangling, 712100, Shaanxi, China.

出版信息

J Nanobiotechnology. 2018 Apr 25;16(1):44. doi: 10.1186/s12951-018-0370-1.

DOI:10.1186/s12951-018-0370-1
PMID:29695232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5916727/
Abstract

BACKGROUND

Single-walled carbon nanotubes (SWCNTs) have many potential applications in various fields. Especially, the unique physicochemical properties make them as the prime candidates for applications in biomedical fields. However, biocompatibility of SWCNTs has been a major concern for their applications. In the study, biocompatibility of oxidized SWCNTs (O-SWCNTs) was assessed using Saccharomyces cerevisiae (S. cerevisiae) as a model organism.

RESULTS

Cell proliferation and viability were significantly changed after exposure to O-SWCNTs (188.2 and 376.4 mg/L) for 24 h. O-SWCNTs were internalized in cells and distributed in cytoplasm, vesicles, lysosomes and cell nucleus. The average O-SWCNTs contents in S. cerevisiae were ranged from 0.18 to 4.82 mg/g during the exposure from 0 to 24 h, and the maximum content was reached at 18 h after exposure. Both penetration and endocytosis were involved in the internalization of O-SWCNTs in S. cerevisiae, and endocytosis was the main pathway. Cellular structures and morphology were changed after exposure to O-SWCNTs, such as undulating appearance at the membrane, shrinking of the cytosol, increased numbers of lipid droplets and disruption of vacuoles. ROS and antioxidant enzymes activities were observably changed following exposure. For the treatment at 376.4 mg/L, 20.8% of the total cells was undergone apoptosis. Decrease of mitochondrial transmembrane potential and leakage of cytochrome c from mitochondria were observed after exposure. Moreover, expression levels of apoptosis-related genes were significantly increased.

CONCLUSIONS

O-SWCNTs can internalize in S. cerevisiae cells via direct penetration and endocytosis, and distribute in cytoplasm, vesicles, lysosomes and cell nucleus. Besides, O-SWCNTs (188.2 and 376.4 mg/L) can induce apoptosis in S. cerevisiae cells, and oxidative stress is involved in activation of the mitochondria-dependent apoptotic pathway.

摘要

背景

单壁碳纳米管(SWCNTs)在各个领域都有许多潜在的应用。特别是,它们独特的物理化学性质使它们成为生物医学领域应用的首选。然而,SWCNTs 的生物相容性一直是它们应用的主要关注点。在这项研究中,以酿酒酵母(Saccharomyces cerevisiae)作为模式生物,评估了氧化 SWCNTs(O-SWCNTs)的生物相容性。

结果

暴露于 O-SWCNTs(188.2 和 376.4 mg/L)24 小时后,细胞增殖和活力明显改变。O-SWCNTs 被细胞内化,并分布在细胞质、囊泡、溶酶体和细胞核中。在暴露 0 至 24 小时期间,酿酒酵母中的平均 O-SWCNTs 含量范围为 0.18 至 4.82 mg/g,暴露 18 小时后达到最大值。在酿酒酵母中,O-SWCNTs 的内化既涉及穿透也涉及内吞作用,内吞作用是主要途径。暴露于 O-SWCNTs 后,细胞结构和形态发生变化,如细胞膜起伏、细胞质收缩、脂质滴数量增加和液泡破裂。暴露后 ROS 和抗氧化酶活性明显改变。在 376.4 mg/L 的处理下,有 20.8%的总细胞发生凋亡。暴露后观察到线粒体跨膜电位下降和细胞色素 c 从线粒体漏出。此外,凋亡相关基因的表达水平显著增加。

结论

O-SWCNTs 可以通过直接穿透和内吞作用进入酿酒酵母细胞,并分布在细胞质、囊泡、溶酶体和细胞核中。此外,O-SWCNTs(188.2 和 376.4 mg/L)可诱导酿酒酵母细胞凋亡,氧化应激参与激活线粒体依赖性凋亡途径。

相似文献

1
Biocompatibility assessment of single-walled carbon nanotubes using Saccharomyces cerevisiae as a model organism.使用酿酒酵母作为模式生物评估单壁碳纳米管的生物相容性。
J Nanobiotechnology. 2018 Apr 25;16(1):44. doi: 10.1186/s12951-018-0370-1.
2
Toxicological effects of multi-walled carbon nanotubes on Saccharomyces cerevisiae: The uptake kinetics and mechanisms and the toxic responses.多壁碳纳米管对酿酒酵母的毒理学效应:摄取动力学和机制及毒性反应。
J Hazard Mater. 2016 Nov 15;318:650-662. doi: 10.1016/j.jhazmat.2016.07.049. Epub 2016 Jul 21.
3
Single-walled and multiwalled carbon nanotubes induce oxidative stress in isolated rat brain mitochondria.单壁和多壁碳纳米管在分离的大鼠脑线粒体中诱导氧化应激。
Toxicol Ind Health. 2019 Jul;35(7):497-506. doi: 10.1177/0748233719856983. Epub 2019 Jul 4.
4
Effect of polyethylene glycol surface charge functionalization of SWCNT on the in vitro and in vivo nanotoxicity and biodistribution monitored noninvasively using MRI.使用 MRI 进行非侵入性监测,研究聚乙二醇表面电荷功能化对 SWCNT 的体外和体内纳米毒性和生物分布的影响。
Toxicol Mech Methods. 2019 May;29(4):233-243. doi: 10.1080/15376516.2018.1540674. Epub 2019 Feb 18.
5
The developmental toxicity, bioaccumulation and distribution of oxidized single walled carbon nanotubes in .氧化单壁碳纳米管在……中的发育毒性、生物累积和分布
Toxicol Res (Camb). 2018 May 3;7(5):897-906. doi: 10.1039/c8tx00084k. eCollection 2018 Sep 1.
6
Development toxicity of functionalized single-walled carbon nanotubes on rare minnow embryos and larvae.功能化单壁碳纳米管对稀有鮈鲫胚胎和幼体的发育毒性
Nanotoxicology. 2015;9(5):579-90. doi: 10.3109/17435390.2014.957253. Epub 2014 Sep 11.
7
Cytotoxicity of single-walled carbon nanotubes on PC12 cells.单壁碳纳米管对 PC12 细胞的细胞毒性。
Toxicol In Vitro. 2011 Feb;25(1):242-50. doi: 10.1016/j.tiv.2010.11.010. Epub 2010 Nov 19.
8
Combined effect of single-walled carbon nanotubes and cadmium on human lung cancer cells.单壁碳纳米管和镉对人肺癌细胞的联合效应。
Environ Sci Pollut Res Int. 2022 Dec;29(58):87844-87857. doi: 10.1007/s11356-022-21933-0. Epub 2022 Jul 12.
9
Biocompatibility assessment of FeO nanoparticles using Saccharomyces cerevisiae as a model organism.使用酿酒酵母作为模式生物评估 FeO 纳米颗粒的生物相容性。
Comp Biochem Physiol C Toxicol Pharmacol. 2020 Jan;227:108645. doi: 10.1016/j.cbpc.2019.108645. Epub 2019 Oct 22.
10
Vitamin E renders protection to PC12 cells against oxidative damage and apoptosis induced by single-walled carbon nanotubes.维生素 E 可保护 PC12 细胞免受单壁碳纳米管诱导的氧化损伤和细胞凋亡。
Toxicol In Vitro. 2012 Feb;26(1):32-41. doi: 10.1016/j.tiv.2011.10.004. Epub 2011 Oct 13.

引用本文的文献

1
Recent Advances in Two-Dimensional MXene-Based Electrochemical Biosensors for Sweat Analysis.二维 MXene 基电化学生物传感器在汗液分析中的最新进展。
Molecules. 2023 Jun 7;28(12):4617. doi: 10.3390/molecules28124617.
2
A Nanobody-Mediated Virus-Targeting Drug Delivery Platform for the Central Nervous System Viral Disease Therapy.一种用于中枢神经系统病毒病治疗的纳米体介导的病毒靶向药物传递平台。
Microbiol Spectr. 2021 Dec 22;9(3):e0148721. doi: 10.1128/Spectrum.01487-21. Epub 2021 Nov 24.
3
Low Toxicological Impact of Commercial Pristine Multi-Walled Carbon Nanotubes on the Yeast .

本文引用的文献

1
Mitochondrial impairment and oxidative stress mediated apoptosis induced by α-FeO nanoparticles in .α-FeO纳米颗粒介导的线粒体损伤和氧化应激诱导的细胞凋亡
Toxicol Res (Camb). 2017 Jul 18;6(5):719-728. doi: 10.1039/c7tx00123a. eCollection 2017 Sep 1.
2
Toxicological effects of graphene oxide on .氧化石墨烯对……的毒理学效应
Toxicol Res (Camb). 2017 May 26;6(4):535-543. doi: 10.1039/c7tx00103g. eCollection 2017 Jul 1.
3
Mitochondrial oxidative stress and dysfunction induced by single- and multiwall carbon nanotubes: A comparative study.
商用原始多壁碳纳米管对酵母的低毒理学影响
Nanomaterials (Basel). 2021 Sep 1;11(9):2272. doi: 10.3390/nano11092272.
4
Comparative and mechanistic toxicity assessment of structure-dependent toxicity of carbon-based nanomaterials.基于结构的碳基纳米材料毒性的比较和机制毒性评估。
J Hazard Mater. 2021 Sep 15;418:126282. doi: 10.1016/j.jhazmat.2021.126282. Epub 2021 Jun 2.
5
Mapping Single Walled Carbon Nanotubes in Photosynthetic Algae by Single-Cell Confocal Raman Microscopy.通过单细胞共聚焦拉曼显微镜对光合藻类中的单壁碳纳米管进行成像
Materials (Basel). 2020 Nov 13;13(22):5121. doi: 10.3390/ma13225121.
6
Commonalities and Differences in the Transcriptional Response of the Model Fungus to Different Commercial Graphene Oxide Materials.模式真菌对不同商业氧化石墨烯材料转录反应的共性与差异
Front Microbiol. 2020 Aug 11;11:1943. doi: 10.3389/fmicb.2020.01943. eCollection 2020.
7
Indocyanine Green-Parthenolide Thermosensitive Liposome Combination Treatment for Triple-Negative Breast Cancer.吲哚菁绿-姜黄素热敏脂质体联合治疗三阴性乳腺癌。
Int J Nanomedicine. 2020 May 5;15:3193-3206. doi: 10.2147/IJN.S245289. eCollection 2020.
8
Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets.模型真菌酿酒酵母对不同浓度商用石墨烯纳米片的毒理学反应。
Sci Rep. 2020 Feb 24;10(1):3232. doi: 10.1038/s41598-020-60101-7.
9
Application of antigen presenting cell-targeted nanovaccine delivery system in rhabdovirus disease prophylactics using fish as a model organism.抗原呈递细胞靶向纳米疫苗传递系统在以鱼类为模式生物的弹状病毒病预防中的应用。
J Nanobiotechnology. 2020 Jan 30;18(1):24. doi: 10.1186/s12951-020-0584-x.
10
Interaction Analysis of Commercial Graphene Oxide Nanoparticles with Unicellular Systems and Biomolecules.商用氧化石墨烯纳米颗粒与单细胞系统和生物分子的相互作用分析。
Int J Mol Sci. 2019 Dec 27;21(1):205. doi: 10.3390/ijms21010205.
单壁和多壁碳纳米管诱导的线粒体氧化应激与功能障碍:一项比较研究。
J Biomed Mater Res A. 2017 Jul;105(7):2047-2055. doi: 10.1002/jbm.a.36063. Epub 2017 May 15.
4
Toxicological effects of multi-walled carbon nanotubes on Saccharomyces cerevisiae: The uptake kinetics and mechanisms and the toxic responses.多壁碳纳米管对酿酒酵母的毒理学效应:摄取动力学和机制及毒性反应。
J Hazard Mater. 2016 Nov 15;318:650-662. doi: 10.1016/j.jhazmat.2016.07.049. Epub 2016 Jul 21.
5
Carbon Nanotubes in Biomedical Applications: Factors, Mechanisms, and Remedies of Toxicity.生物医学应用中的碳纳米管:毒性因素、机制及应对措施
J Med Chem. 2016 Sep 22;59(18):8149-67. doi: 10.1021/acs.jmedchem.5b01770. Epub 2016 May 27.
6
A review of toxicity studies of single-walled carbon nanotubes in laboratory animals.实验室动物中单壁碳纳米管毒性研究综述。
Regul Toxicol Pharmacol. 2016 Feb;74:42-63. doi: 10.1016/j.yrtph.2015.11.015. Epub 2015 Nov 24.
7
Acute toxicity comparison of single-walled carbon nanotubes in various freshwater organisms.单壁碳纳米管在多种淡水生物中的急性毒性比较
Biomed Res Int. 2015;2015:323090. doi: 10.1155/2015/323090. Epub 2015 Jan 14.
8
Carbon nanotubes: potential medical applications and safety concerns.碳纳米管:潜在的医学应用和安全隐患。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2015 May-Jun;7(3):371-86. doi: 10.1002/wnan.1317. Epub 2014 Nov 27.
9
Acrolein-Induced Oxidative Stress and Cell Death Exhibiting Features of Apoptosis in the Yeast Saccharomyces cerevisiae Deficient in SOD1.在缺乏超氧化物歧化酶1(SOD1)的酿酒酵母中,丙烯醛诱导的氧化应激和细胞死亡呈现出凋亡特征。
Cell Biochem Biophys. 2015 Apr;71(3):1525-36. doi: 10.1007/s12013-014-0376-8.
10
Toxicity of single-walled carbon nanotubes.单壁碳纳米管的毒性
Arch Toxicol. 2016 Jan;90(1):103-18. doi: 10.1007/s00204-014-1376-6. Epub 2014 Oct 2.