Cargando…

Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells

Inflammasomes are cytosolic complexes composed of a Nod-like receptor, NLR, the adaptor protein, ASC, and a proteolytic enzyme, caspase-1. Inflammasome activation leads to caspase-1 activation and promotes functional maturation of IL-1β and IL-18, two prototypical inflammatory cytokines. Besides, in...

Descripción completa

Detalles Bibliográficos
Autores principales: de Melo, Fernando Menegatti, Kawasaki, Karine, Sellani, Tarciso Almeida, Bonifácio, Bruno Souza, Mortara, Renato Arruda, Toma, Henrique Eisi, de Melo, Filipe Menegatti, Rodrigues, Elaine Guadelupe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502261/
https://www.ncbi.nlm.nih.gov/pubmed/36144933
http://dx.doi.org/10.3390/nano12183145
_version_ 1784795662073724928
author de Melo, Fernando Menegatti
Kawasaki, Karine
Sellani, Tarciso Almeida
Bonifácio, Bruno Souza
Mortara, Renato Arruda
Toma, Henrique Eisi
de Melo, Filipe Menegatti
Rodrigues, Elaine Guadelupe
author_facet de Melo, Fernando Menegatti
Kawasaki, Karine
Sellani, Tarciso Almeida
Bonifácio, Bruno Souza
Mortara, Renato Arruda
Toma, Henrique Eisi
de Melo, Filipe Menegatti
Rodrigues, Elaine Guadelupe
author_sort de Melo, Fernando Menegatti
collection PubMed
description Inflammasomes are cytosolic complexes composed of a Nod-like receptor, NLR, the adaptor protein, ASC, and a proteolytic enzyme, caspase-1. Inflammasome activation leads to caspase-1 activation and promotes functional maturation of IL-1β and IL-18, two prototypical inflammatory cytokines. Besides, inflammasome activation leads to pyroptosis, an inflammatory type of cell death. Inflammasomes are vital for the host to cope with foreign pathogens or tissue damage. Herein, we show that quantum-dot-based iron oxide nanoparticles, MNP@QD, trigger NLRP3 inflammasome activation and subsequent release of proinflammatory interleukin IL-1β by murine bone marrow-derived dendritic cells (BMDCs). This activation is more pronounced if these cells endocytose the nanoparticles before receiving inflammatory stimulation. MNP@QD was characterized by using imaging techniques like transmission electron microscopy, fluorescence microscopy, and atomic force microscopy, as well as physical and spectroscopical techniques such as fluorescence spectroscopy and powder diffraction. These findings may open the possibility of using the composite MNP@QD as both an imaging and a therapeutic tool.
format Online
Article
Text
id pubmed-9502261
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95022612022-09-24 Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells de Melo, Fernando Menegatti Kawasaki, Karine Sellani, Tarciso Almeida Bonifácio, Bruno Souza Mortara, Renato Arruda Toma, Henrique Eisi de Melo, Filipe Menegatti Rodrigues, Elaine Guadelupe Nanomaterials (Basel) Article Inflammasomes are cytosolic complexes composed of a Nod-like receptor, NLR, the adaptor protein, ASC, and a proteolytic enzyme, caspase-1. Inflammasome activation leads to caspase-1 activation and promotes functional maturation of IL-1β and IL-18, two prototypical inflammatory cytokines. Besides, inflammasome activation leads to pyroptosis, an inflammatory type of cell death. Inflammasomes are vital for the host to cope with foreign pathogens or tissue damage. Herein, we show that quantum-dot-based iron oxide nanoparticles, MNP@QD, trigger NLRP3 inflammasome activation and subsequent release of proinflammatory interleukin IL-1β by murine bone marrow-derived dendritic cells (BMDCs). This activation is more pronounced if these cells endocytose the nanoparticles before receiving inflammatory stimulation. MNP@QD was characterized by using imaging techniques like transmission electron microscopy, fluorescence microscopy, and atomic force microscopy, as well as physical and spectroscopical techniques such as fluorescence spectroscopy and powder diffraction. These findings may open the possibility of using the composite MNP@QD as both an imaging and a therapeutic tool. MDPI 2022-09-10 /pmc/articles/PMC9502261/ /pubmed/36144933 http://dx.doi.org/10.3390/nano12183145 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Melo, Fernando Menegatti
Kawasaki, Karine
Sellani, Tarciso Almeida
Bonifácio, Bruno Souza
Mortara, Renato Arruda
Toma, Henrique Eisi
de Melo, Filipe Menegatti
Rodrigues, Elaine Guadelupe
Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title_full Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title_fullStr Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title_full_unstemmed Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title_short Quantum-Dot-Based Iron Oxide Nanoparticles Activate the NLRP3 Inflammasome in Murine Bone Marrow-Derived Dendritic Cells
title_sort quantum-dot-based iron oxide nanoparticles activate the nlrp3 inflammasome in murine bone marrow-derived dendritic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502261/
https://www.ncbi.nlm.nih.gov/pubmed/36144933
http://dx.doi.org/10.3390/nano12183145
work_keys_str_mv AT demelofernandomenegatti quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT kawasakikarine quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT sellanitarcisoalmeida quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT bonifaciobrunosouza quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT mortararenatoarruda quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT tomahenriqueeisi quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT demelofilipemenegatti quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells
AT rodrigueselaineguadelupe quantumdotbasedironoxidenanoparticlesactivatethenlrp3inflammasomeinmurinebonemarrowderiveddendriticcells