Influence of bovine serum albumin pre-incubation on toxicity and ER stress-apoptosis gene expression in THP-1 macrophages exposed to ZnO nanoparticles
- PMID: 29783874
- DOI: 10.1080/15376516.2018.1479907
Influence of bovine serum albumin pre-incubation on toxicity and ER stress-apoptosis gene expression in THP-1 macrophages exposed to ZnO nanoparticles
Abstract
When entering a biological environment, proteins could be adsorbed onto nanoparticles (NPs), which can potentially influence the toxicity of NPs. This study used bovine serum albumin (BSA) as the model for serum protein and investigated its interactions with three different types of ZnO NPs, coded as XFI06 (pristine NPs of 20 nm), NM110 (pristine NPs of 100 nm) and NM111 (hydrophobic NPs of 130 nm). Atomic force microscope indicated the adsorption of BSA to ZnO NPs, leading to the increase of NP diameters. Pre-incubation with BSA did not significantly affect hydrodynamic size but decreased Zeta potential of NM110 and NM111. The fluorescence and synchronous fluorescence of BSA were quenched after pre-incubation with ZnO NPs, and the quenching effects were more obvious for XFI06 and NM110. Exposure to all types of ZnO NPs significantly induced cytotoxicity and lysosomal destabilization, which was slightly alleviated when NPs were pre-incubated with BSA. However, ZnO NPs with or without pre-incubation of BSA resulted in comparable intracellular Zn ions, glutathione and reactive oxygen species in THP-1 macrophages. Exposure to ZnO NPs promoted the expression of endoplasmic reticulum (ER) stress markers (DDIT3 and XBP-1s) and apoptosis genes (CASP9 and CASP12). Pre-incubation with BSA had minimal impact on ER stress gene expression but decreased apoptosis gene expression. Combined, these results suggested that pre-incubation with BSA could modestly alleviate the cytotoxicity and reduce ER stress related apoptosis gene expression in THP-1 macrophages after ZnO NP exposure.
Keywords: THP-1 macrophages; ZnO nanoparticles (NPs); bovine serum albumin (BSA); cytotoxicity; endoplasmic reticulum (ER) stress.
Similar articles
-
Influence of pristine and hydrophobic ZnO nanoparticles on cytotoxicity and endoplasmic reticulum (ER) stress-autophagy-apoptosis gene expression in A549-macrophage co-culture.Ecotoxicol Environ Saf. 2019 Jan 15;167:188-195. doi: 10.1016/j.ecoenv.2018.10.018. Epub 2018 Oct 16. Ecotoxicol Environ Saf. 2019. PMID: 30340083
-
Toxicity of ZnO nanoparticles (NPs) to THP-1 macrophages: interactions with saturated or unsaturated free fatty acids.Toxicol Mech Methods. 2019 May;29(4):291-299. doi: 10.1080/15376516.2018.1550130. Epub 2019 Jan 16. Toxicol Mech Methods. 2019. PMID: 30461332
-
Toxicity of ZnO nanoparticles (NPs) with or without hydrophobic surface coating to THP-1 macrophages: interactions with BSA or oleate-BSA.Toxicol Mech Methods. 2018 Sep;28(7):520-528. doi: 10.1080/15376516.2018.1469708. Epub 2018 May 16. Toxicol Mech Methods. 2018. PMID: 29697006
-
A review of endoplasmic reticulum (ER) stress and nanoparticle (NP) exposure.Life Sci. 2017 Oct 1;186:33-42. doi: 10.1016/j.lfs.2017.08.003. Epub 2017 Aug 4. Life Sci. 2017. PMID: 28782531 Review.
-
Biological reactivity of zinc oxide nanoparticles with mammalian test systems: an overview.Nanomedicine (Lond). 2015;10(13):2075-92. doi: 10.2217/nnm.15.44. Epub 2015 Jul 2. Nanomedicine (Lond). 2015. PMID: 26135328 Review.
Cited by
-
The cytotoxicity of zinc oxide nanoparticles to 3D brain organoids results from excessive intracellular zinc ions and defective autophagy.Cell Biol Toxicol. 2023 Feb;39(1):259-275. doi: 10.1007/s10565-021-09678-x. Epub 2021 Nov 11. Cell Biol Toxicol. 2023. PMID: 34766255
-
Assessing cytotoxicity and endoplasmic reticulum stress in human blood-brain barrier cells due to silver and copper oxide nanoparticles.J Appl Genet. 2024 Feb 9. doi: 10.1007/s13353-024-00833-8. Online ahead of print. J Appl Genet. 2024. PMID: 38332387
-
Toxicity of combined exposure of ZnO nanoparticles (NPs) and myricetin to Caco-2 cells: changes of NP colloidal aspects, NP internalization and the apoptosis-endoplasmic reticulum stress pathway.Toxicol Res (Camb). 2019 Jun 20;8(5):613-620. doi: 10.1039/c9tx00127a. eCollection 2019 Sep 1. Toxicol Res (Camb). 2019. PMID: 31588339 Free PMC article.
-
Transcriptomic-based toxicological investigations of graphene oxide with modest cytotoxicity to human umbilical vein endothelial cells: changes of Toll-like receptor signaling pathways.Toxicol Res (Camb). 2021 Oct 16;10(6):1104-1115. doi: 10.1093/toxres/tfab091. eCollection 2021 Dec. Toxicol Res (Camb). 2021. PMID: 34956614 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous