Modification of MWCNTs with Bi2WO6 nanoparticles targeting IL-1β and NLRP3 inflammasome via augmented autophagy.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 02 05 2024
accepted: 10 08 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 31 10 2024
Statut: epublish

Résumé

This study reports the facile hydrothermal synthesis of pure Bi2WO6 and Bi2WO6\MWCNTs nanocomposite at specific molar ratio 1:2.5 of Bi2WO6:MWCNTs and elucidates their role in modulating the NLRP3 inflammasome pathway via autophagy induction. Comprehensive characterization techniques, including XRD, Raman, UV.Vis PL,FESEM,EDS and TEM, revealed the successful incorporation of MWCNTs into the Bi2WO6 structures, leading to enhanced crystattlinity, reduced band gap energy (2.4 eV) suppressed charge carrier recombination and mitigated nanoparticles aggregation. Notably, the reduced band gap facikitaed improved visible light harvesting, a crucial attribute for photocatalytic applications. Significantly, the nanocompsoite exhibited a remarkable capacity to augment autophagy in bone marrow-derived macrophages (BMDMs), consequently down-regulating the NLRP3 inflammasom activation and IL-1β secretion upon LPS and ATP stimulation. Immunofluorescence assays unveiled increased co-localization of LC3 and NLRP3, suggestion enhanced targeting of NLRP3 by autophagy. Inhibition of autophagy by 3-MA reversed these effects, confirming the pivotal role of autophagy induction. Furthermore, the nanocomposite attenuated caspase-1 activation and ASC oligomerzation, thereby impeding inflammasome assembly. Collectively, these findings underscore the potential of Bi2WO6\MWCNTs nanocompsite as a multifaceted therapeutic platform, levering its tailored optoelectronic properties and sbility to modulate the NLRP3 infalmmasome via autophagy augmentation. This work covers the way for the development of advanced nanomaterials with tunable functionalities for combating inflammatory disorders and antimicrobial applications.

Identifiants

pubmed: 39480754
doi: 10.1371/journal.pone.0309389
pii: PONE-D-24-15368
doi:

Substances chimiques

NLR Family, Pyrin Domain-Containing 3 Protein 0
Inflammasomes 0
Interleukin-1beta 0
Nlrp3 protein, mouse 0
Tungsten Compounds 0
Caspase 1 EC 3.4.22.36

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0309389

Informations de copyright

Copyright: © 2024 Rahoomi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Zenaa R Rahoomi (ZR)

Ibn Sina University of Medical and Pharmaceutical Science, Baghdad, Iraq.
Department of Applied Sciences, University of Technology- Iraq, Baghdad, Iraq.

Duha S Ahmed (DS)

Department of Applied Sciences, University of Technology- Iraq, Baghdad, Iraq.

Majid S Jabir (MS)

Department of Applied Sciences, University of Technology- Iraq, Baghdad, Iraq.

Haney Samir (H)

Department of Veterinary Medicine, Tokyo University of Agriculture and Technology, Fuchu, Japan.

Ayman A Swelum (AA)

Department of Animal Production, College of Food and Agriculture Science, King Saud University, Riyadh, Saudi Arabia.

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Classifications MeSH