The Toxicity of Nanoparticles to Human Endothelial Cells
- PMID: 29453532
- DOI: 10.1007/978-3-319-72041-8_4
The Toxicity of Nanoparticles to Human Endothelial Cells
Abstract
The use of nanoparticles (NPs) in commercially available products and as biomedicinal materials could lead to increasing contact of human blood vessels with NPs, and it is necessary to assess the potential adverse effects of NPs to cells lining blood vessels. Of them, endothelial cells (ECs) are of particular relevance as they play a crucial role in the regulation of function of blood vessels. In this book chapter, I discussed studies that used human ECs to study the toxicity and mechanisms of NPs. It has been shown that exposure of human ECs to NPs could lead to cytotoxicity, genotoxicity, endothelial activation and impaired NO signaling. Oxidative stress and inflammation induced by NPs have been suggested as the mechanisms associated with the toxicity of NPs to ECs, and a three-tier model has been proposed to explain the association between NP induced oxidative stress and toxicity. In recent years, dysfunction of autophagy (excessive autophagy induction) has also been suggested as one of the mechanisms associated with the toxicity of NPs to human ECs. In the future, it is necessary to use human ECs to assess the toxicity of NPs to better understand the potential adverse effects of NPs entering circulation.
Keywords: Endothelial activation; Endothelial cell (EC); Genotoxicity; Nanoparticle (NP); Oxidative stress.
Similar articles
-
The use of human umbilical vein endothelial cells (HUVECs) as an in vitro model to assess the toxicity of nanoparticles to endothelium: a review.J Appl Toxicol. 2017 Dec;37(12):1359-1369. doi: 10.1002/jat.3470. Epub 2017 Apr 6. J Appl Toxicol. 2017. PMID: 28383141 Review.
-
Induction of oxidative stress, lysosome activation and autophagy by nanoparticles in human brain-derived endothelial cells.Biochem J. 2012 Feb 1;441(3):813-21. doi: 10.1042/BJ20111252. Biochem J. 2012. PMID: 22026563
-
Assessment of the lung toxicity of copper oxide nanoparticles: current status.Nanomedicine (Lond). 2015;10(15):2365-77. doi: 10.2217/nnm.15.72. Epub 2015 Aug 7. Nanomedicine (Lond). 2015. PMID: 26251192
-
High-Content Imaging and Gene Expression Approaches To Unravel the Effect of Surface Functionality on Cellular Interactions of Silver Nanoparticles.ACS Nano. 2015 Oct 27;9(10):10431-44. doi: 10.1021/acsnano.5b04661. Epub 2015 Sep 3. ACS Nano. 2015. PMID: 26327399
-
Nanoparticles: molecular targets and cell signalling.Arch Toxicol. 2011 Jul;85(7):733-41. doi: 10.1007/s00204-010-0546-4. Epub 2010 May 26. Arch Toxicol. 2011. PMID: 20502881 Review.
Cited by
-
Air Pollution Exposure Induces Vascular Injury and Hampers Endothelial Repair by Altering Progenitor and Stem Cells Functionality.Front Cell Dev Biol. 2022 May 27;10:897831. doi: 10.3389/fcell.2022.897831. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35712669 Free PMC article. Review.
-
Dietary supplementation with copper nanoparticles influences the markers of oxidative stress and modulates vasodilation of thoracic arteries in young Wistar rats.PLoS One. 2020 Feb 21;15(2):e0229282. doi: 10.1371/journal.pone.0229282. eCollection 2020. PLoS One. 2020. PMID: 32084205 Free PMC article.
-
Bismuth Oxide (Bi2O3) Nanoparticles Cause Selective Toxicity in a Human Endothelial (HUVE) Cell Line Compared to Epithelial Cells.Toxics. 2023 Apr 4;11(4):343. doi: 10.3390/toxics11040343. Toxics. 2023. PMID: 37112570 Free PMC article.
-
Therapeutic Nanoparticles for the Different Phases of Ischemic Stroke.Life (Basel). 2021 May 26;11(6):482. doi: 10.3390/life11060482. Life (Basel). 2021. PMID: 34073229 Free PMC article. Review.
-
Gadolinium Oxide Nanoparticles Induce Toxicity in Human Endothelial HUVECs via Lipid Peroxidation, Mitochondrial Dysfunction and Autophagy Modulation.Nanomaterials (Basel). 2020 Aug 26;10(9):1675. doi: 10.3390/nano10091675. Nanomaterials (Basel). 2020. PMID: 32859033 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous