Resolution of acute inflammation induced by monosodium urate crystals (MSU) through neutrophil extracellular trap-MSU aggregate-mediated negative signaling

We explored the potential molecular basis for the spontaneous resolution of MSU induced acute inflammation using a cell-based model in that huge NET-MSU aggregates frustrate the transformation of newly entering PMNs to the N2 phenotype, enhancing the production of the anti-inflammatory cytokine IL-1RA.

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Publication Details

Journal
Journal of Inflammation
Published
2024-11-27
DOI
https://doi.org/10.1186/s12950-024-00423-9
Citations
11
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
2.65

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article

Resolution of acute inflammation induced by monosodium urate crystals (MSU) through neutrophil extracellular trap-MSU aggregate-mediated negative signaling

Chieh‐Yu Shen, Song‐Chou Hsieh, Ko‐Jen Li, Chia‐Li Yu et al.
11 citations
Journal of Inflammation
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
2.65
article

Resolution of acute inflammation induced by monosodium urate crystals (MSU) through neutrophil extracellular trap-MSU aggregate-mediated negative signaling

Chieh‐Yu Shen, Song‐Chou Hsieh, Ko‐Jen Li, Chia‐Li Yu, Yu‐Min Kuo, Yu-Hsuan Chen, Cheng‐Hsun Lu, Chih-Hao Wu
article en
11 citations

Abstract

We explored the potential molecular basis for the spontaneous resolution of MSU induced acute inflammation using a cell-based model in that huge NET-MSU aggregates frustrate the transformation of newly entering PMNs to the N2 phenotype, enhancing the production of the anti-inflammatory cytokine IL-1RA.

Journal of InflammationVol. 21(1)
National Taiwan University (TW), National Taiwan University Hospital (TW)
National Science Council, National Taiwan University Hospital, National Taiwan University
Life below water
Openalex Percentile: Top 9%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
2.65
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