Cargando…

PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation

Polymerase 1 and transcript release factor (PTRF, encoding by Cavin-1) regulates interleukin 33 (IL-33) release, which is implicated in asthma development. Z-DNA binding protein 1 (ZBP1)-sensing Z-RNAs induces necroptosis which causes inflammatory diseases. House dust mite (HDM) is the major source...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Juan, Liu, Yahui, Lan, Gelei, Zhou, Yao, Ni, Yingmeng, Liao, Kai, Zheng, Fang, Cheng, Qijian, Shi, Guochao, Su, Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349813/
https://www.ncbi.nlm.nih.gov/pubmed/37454215
http://dx.doi.org/10.1038/s41419-023-05971-1
_version_ 1785074001180098560
author Du, Juan
Liu, Yahui
Lan, Gelei
Zhou, Yao
Ni, Yingmeng
Liao, Kai
Zheng, Fang
Cheng, Qijian
Shi, Guochao
Su, Xiao
author_facet Du, Juan
Liu, Yahui
Lan, Gelei
Zhou, Yao
Ni, Yingmeng
Liao, Kai
Zheng, Fang
Cheng, Qijian
Shi, Guochao
Su, Xiao
author_sort Du, Juan
collection PubMed
description Polymerase 1 and transcript release factor (PTRF, encoding by Cavin-1) regulates interleukin 33 (IL-33) release, which is implicated in asthma development. Z-DNA binding protein 1 (ZBP1)-sensing Z-RNAs induces necroptosis which causes inflammatory diseases. House dust mite (HDM) is the major source of allergen in house dust and is strongly associated with the development of asthma. Whether PTRF via IL-33 and ZBP1 mediates HDM-induced macrophage necroptosis and airway inflammation remains unclear. Here, we found that deficiency of PTRF could reduce lung IL-33, ZBP1, phosphor-receptor-interacting protein kinase 3 (p-RIPK3), and phosphor-mixed lineage kinase domain-like (p-MLKL) (necroptosis executioner), and airway inflammation in an HDM-induced asthma mouse model. In HDM-treated macrophages, ZBP1, p-RIPK3, and p-MLKL levels were markedly increased, and these changes were reversed by deletion of Cavin-1. Deletion of Il33 also reduced expression of ZBP1, p-RIPK3, and p-MLKL in HDM-challenged lungs. Moreover, IL-33 synergizing with HDM boosted expression of ZBP1, p-RIPK3, and p-MLKL in macrophages. In bronchial epithelial cells rather than macrophages and vascular endothelial cells, PTRF positively regulates IL-33 expression. Therefore, we conclude that PTRF mediates HDM-induced macrophage ZBP1/necroptosis and airway inflammation, and this effect could be boosted by bronchial epithelial cell-derived IL-33. Our findings suggest that PTRF-IL33-ZBP1 signaling pathway might be a promising target for dampening airway inflammation.
format Online
Article
Text
id pubmed-10349813
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-103498132023-07-17 PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation Du, Juan Liu, Yahui Lan, Gelei Zhou, Yao Ni, Yingmeng Liao, Kai Zheng, Fang Cheng, Qijian Shi, Guochao Su, Xiao Cell Death Dis Article Polymerase 1 and transcript release factor (PTRF, encoding by Cavin-1) regulates interleukin 33 (IL-33) release, which is implicated in asthma development. Z-DNA binding protein 1 (ZBP1)-sensing Z-RNAs induces necroptosis which causes inflammatory diseases. House dust mite (HDM) is the major source of allergen in house dust and is strongly associated with the development of asthma. Whether PTRF via IL-33 and ZBP1 mediates HDM-induced macrophage necroptosis and airway inflammation remains unclear. Here, we found that deficiency of PTRF could reduce lung IL-33, ZBP1, phosphor-receptor-interacting protein kinase 3 (p-RIPK3), and phosphor-mixed lineage kinase domain-like (p-MLKL) (necroptosis executioner), and airway inflammation in an HDM-induced asthma mouse model. In HDM-treated macrophages, ZBP1, p-RIPK3, and p-MLKL levels were markedly increased, and these changes were reversed by deletion of Cavin-1. Deletion of Il33 also reduced expression of ZBP1, p-RIPK3, and p-MLKL in HDM-challenged lungs. Moreover, IL-33 synergizing with HDM boosted expression of ZBP1, p-RIPK3, and p-MLKL in macrophages. In bronchial epithelial cells rather than macrophages and vascular endothelial cells, PTRF positively regulates IL-33 expression. Therefore, we conclude that PTRF mediates HDM-induced macrophage ZBP1/necroptosis and airway inflammation, and this effect could be boosted by bronchial epithelial cell-derived IL-33. Our findings suggest that PTRF-IL33-ZBP1 signaling pathway might be a promising target for dampening airway inflammation. Nature Publishing Group UK 2023-07-15 /pmc/articles/PMC10349813/ /pubmed/37454215 http://dx.doi.org/10.1038/s41419-023-05971-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Du, Juan
Liu, Yahui
Lan, Gelei
Zhou, Yao
Ni, Yingmeng
Liao, Kai
Zheng, Fang
Cheng, Qijian
Shi, Guochao
Su, Xiao
PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title_full PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title_fullStr PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title_full_unstemmed PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title_short PTRF-IL33-ZBP1 signaling mediating macrophage necroptosis contributes to HDM-induced airway inflammation
title_sort ptrf-il33-zbp1 signaling mediating macrophage necroptosis contributes to hdm-induced airway inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349813/
https://www.ncbi.nlm.nih.gov/pubmed/37454215
http://dx.doi.org/10.1038/s41419-023-05971-1
work_keys_str_mv AT dujuan ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT liuyahui ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT langelei ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT zhouyao ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT niyingmeng ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT liaokai ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT zhengfang ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT chengqijian ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT shiguochao ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation
AT suxiao ptrfil33zbp1signalingmediatingmacrophagenecroptosiscontributestohdminducedairwayinflammation