Assessing cytotoxicity and endoplasmic reticulum stress in human blood-brain barrier cells due to silver and copper oxide nanoparticles.

Copper oxide nanoparticles Cytotoxicity Endoplasmic reticulum stress-induction Human cerebral microvessel endothelial cells Silver nanoparticles

Journal

Journal of applied genetics
ISSN: 2190-3883
Titre abrégé: J Appl Genet
Pays: England
ID NLM: 9514582

Informations de publication

Date de publication:
09 Feb 2024
Historique:
received: 08 09 2023
accepted: 18 01 2024
revised: 17 01 2024
medline: 9 2 2024
pubmed: 9 2 2024
entrez: 9 2 2024
Statut: aheadofprint

Résumé

In recent years, it has been generally accepted that metal-based nanoparticles (NPs) may induce stress in the endoplasmic reticulum (ER), a key organelle where protein folding occurs. We examined ER stress in immortalized human cerebral microvascular cells (hCMEC/D3) after exposure to silver-NPs (Ag-NPs)- and copper oxide-NPs (CuO-NPs) induced toxicity at < 10 nm and < 40 nm or < 50 nm diameters, respectively. In cytotoxicity assessments, cells were exposed to different CuO-NPs (5-400 µg/mL) or Ag-NPs (1-10 µg/mL) concentration ranges for 24 h and 72 h, and tetrazole salt reduction assays (EZ4U) were performed. Also, Ag-NP or CuO-NP effects on cell proliferation, apoptosis (caspase 3/7 assays), and ER stress and cell morphology were evaluated. In ER stress assessments, RNA-like endoplasmic reticulum kinase (PERK), activating transcription factor 6 (ATF6), inositol-requiring enzyme 1 (IRE1a), and others stress factor mRNA levels were determined after 24 h treatment using Real-Time PCR. Increased stress sensors (IRE1a, PERK, and ATF6) mRNA levels were observed after exposure to Ag-NPs (< 10 and < 40 nm) or CuO-NPs (< 50 nm). We investigated the expression of tight junction (TJ) proteins (barrier junctions) and showed that both types of NP reduced of OCLN gene expression. Morphological changes were observed after Ag-NP or CuO-NP exposure using holotomographic microscopy. Our data suggest that Ag- and CuO-NPs should undergo future in vitro and in vivo toxicology studies, especially for downstream biomedical application and occupational risk assessments.

Identifiants

pubmed: 38332387
doi: 10.1007/s13353-024-00833-8
pii: 10.1007/s13353-024-00833-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

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Auteurs

Luiza Chojnacka-Puchta (L)

Central Institute for Labour Protection - National Research Institute, Czerniakowska 16, 00-701, Warsaw, Poland. lucho@ciop.pl.

Dorota Sawicka (D)

Central Institute for Labour Protection - National Research Institute, Czerniakowska 16, 00-701, Warsaw, Poland.

Lidia Zapor (L)

Central Institute for Labour Protection - National Research Institute, Czerniakowska 16, 00-701, Warsaw, Poland.

Katarzyna Miranowicz-Dzierzawska (K)

Central Institute for Labour Protection - National Research Institute, Czerniakowska 16, 00-701, Warsaw, Poland.

Classifications MeSH