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Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate

Although intraperitoneal injection of monosodium urate (MSU) is an effective model for studying peritonitis, its establishment remains challenging. Here, we present a protocol for using MSU to activate the NLRP3 inflammasome in bone-marrow-derived macrophages (BMDMs) and to induce peritonitis in mic...

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Detalles Bibliográficos
Autores principales: Liu, Didi, Huang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493585/
https://www.ncbi.nlm.nih.gov/pubmed/37682717
http://dx.doi.org/10.1016/j.xpro.2023.102554
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author Liu, Didi
Huang, Yi
author_facet Liu, Didi
Huang, Yi
author_sort Liu, Didi
collection PubMed
description Although intraperitoneal injection of monosodium urate (MSU) is an effective model for studying peritonitis, its establishment remains challenging. Here, we present a protocol for using MSU to activate the NLRP3 inflammasome in bone-marrow-derived macrophages (BMDMs) and to induce peritonitis in mice. We describe steps for isolating and culturing BMDMs, preparing MSU crystals, and activating the NLRP3 inflammasome using western blot and ELISA. We then detail procedures for inducing peritonitis and testing for relevant indicators using flow cytometry and ELISA. For complete details on the use and execution of this protocol, please refer to Huang et al. (2023).(1)
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spelling pubmed-104935852023-09-12 Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate Liu, Didi Huang, Yi STAR Protoc Protocol Although intraperitoneal injection of monosodium urate (MSU) is an effective model for studying peritonitis, its establishment remains challenging. Here, we present a protocol for using MSU to activate the NLRP3 inflammasome in bone-marrow-derived macrophages (BMDMs) and to induce peritonitis in mice. We describe steps for isolating and culturing BMDMs, preparing MSU crystals, and activating the NLRP3 inflammasome using western blot and ELISA. We then detail procedures for inducing peritonitis and testing for relevant indicators using flow cytometry and ELISA. For complete details on the use and execution of this protocol, please refer to Huang et al. (2023).(1) Elsevier 2023-09-07 /pmc/articles/PMC10493585/ /pubmed/37682717 http://dx.doi.org/10.1016/j.xpro.2023.102554 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Liu, Didi
Huang, Yi
Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title_full Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title_fullStr Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title_full_unstemmed Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title_short Protocol for in vivo and in vitro activation of NLRP3 inflammasome in mice using monosodium urate
title_sort protocol for in vivo and in vitro activation of nlrp3 inflammasome in mice using monosodium urate
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493585/
https://www.ncbi.nlm.nih.gov/pubmed/37682717
http://dx.doi.org/10.1016/j.xpro.2023.102554
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