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The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis
BACKGROUND: Neutrophil extracellular traps (NETs) play an important role in the development and progression of ulcerative colitis (UC). Peptidyl arginine deiminase 4 (PAD4) is essential for the formation of NETs via catalyzing histone citrullination. This study mainly to explore the role of PAD4-med...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10151647/ https://www.ncbi.nlm.nih.gov/pubmed/37143672 http://dx.doi.org/10.3389/fimmu.2023.1144976 |
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author | Wang, Ping Liu, Dan Zhou, Ziqi Liu, Fangjun Shen, Yiming You, Qi Lu, Shiping Wu, Jie |
author_facet | Wang, Ping Liu, Dan Zhou, Ziqi Liu, Fangjun Shen, Yiming You, Qi Lu, Shiping Wu, Jie |
author_sort | Wang, Ping |
collection | PubMed |
description | BACKGROUND: Neutrophil extracellular traps (NETs) play an important role in the development and progression of ulcerative colitis (UC). Peptidyl arginine deiminase 4 (PAD4) is essential for the formation of NETs via catalyzing histone citrullination. This study mainly to explore the role of PAD4-mediated NETs in intestinal inflammation of dextran sulfate sodium (DSS)-induced UC. METHODS: Acute and chronic colitis mouse models were established by supplementing DSS in drinking water. Colon tissues from colitis mice were analyzed for the level of PAD4 expression, citrullinated histone H3(Cit-H3), intestinal histopathology, and inflammatory cytokines secretion. Serum samples were tested for systemic neutrophil activation biomarkers. Colitis mice administered with Cl-amidine, a PAD4 inhibitor, and PAD4 knockout mice were investigated to detect NETs formation, intestinal inflammation, and barrier function. RESULT: We found the formation of NETs significantly increased in DSS-induced colitis mice and was correlated with disease markers. Blocking NETs formation by Cl-amidine or PAD4 genetic knockout could alleviate clinical colitis index, intestinal inflammation, and barrier dysfunction. CONCLUSION: This study provided a research basis for the role of PAD4-mediated NETs formation in the pathogenesis of UC and suggested that inhibition of PAD4 activity and the formation of NETs may be helpful for the prevention and treatment of UC. |
format | Online Article Text |
id | pubmed-10151647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101516472023-05-03 The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis Wang, Ping Liu, Dan Zhou, Ziqi Liu, Fangjun Shen, Yiming You, Qi Lu, Shiping Wu, Jie Front Immunol Immunology BACKGROUND: Neutrophil extracellular traps (NETs) play an important role in the development and progression of ulcerative colitis (UC). Peptidyl arginine deiminase 4 (PAD4) is essential for the formation of NETs via catalyzing histone citrullination. This study mainly to explore the role of PAD4-mediated NETs in intestinal inflammation of dextran sulfate sodium (DSS)-induced UC. METHODS: Acute and chronic colitis mouse models were established by supplementing DSS in drinking water. Colon tissues from colitis mice were analyzed for the level of PAD4 expression, citrullinated histone H3(Cit-H3), intestinal histopathology, and inflammatory cytokines secretion. Serum samples were tested for systemic neutrophil activation biomarkers. Colitis mice administered with Cl-amidine, a PAD4 inhibitor, and PAD4 knockout mice were investigated to detect NETs formation, intestinal inflammation, and barrier function. RESULT: We found the formation of NETs significantly increased in DSS-induced colitis mice and was correlated with disease markers. Blocking NETs formation by Cl-amidine or PAD4 genetic knockout could alleviate clinical colitis index, intestinal inflammation, and barrier dysfunction. CONCLUSION: This study provided a research basis for the role of PAD4-mediated NETs formation in the pathogenesis of UC and suggested that inhibition of PAD4 activity and the formation of NETs may be helpful for the prevention and treatment of UC. Frontiers Media S.A. 2023-04-18 /pmc/articles/PMC10151647/ /pubmed/37143672 http://dx.doi.org/10.3389/fimmu.2023.1144976 Text en Copyright © 2023 Wang, Liu, Zhou, Liu, Shen, You, Lu and Wu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Wang, Ping Liu, Dan Zhou, Ziqi Liu, Fangjun Shen, Yiming You, Qi Lu, Shiping Wu, Jie The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title | The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title_full | The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title_fullStr | The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title_full_unstemmed | The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title_short | The role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
title_sort | role of protein arginine deiminase 4-dependent neutrophil extracellular traps formation in ulcerative colitis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10151647/ https://www.ncbi.nlm.nih.gov/pubmed/37143672 http://dx.doi.org/10.3389/fimmu.2023.1144976 |
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