Mincle/Syk Signalling Promotes Intestinal Mucosal Inflammation Through Induction of Macrophage Pyroptosis in Crohn's Disease.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
02 Dec 2020
Historique:
pubmed: 26 4 2020
medline: 3 2 2022
entrez: 26 4 2020
Statut: ppublish

Résumé

Macrophage-inducible C-type lectin [Mincle] signalling plays a proinflammatory role in different organs such as the brain and liver, but its role in intestinal inflammation, including Crohn's disease [CD], remains unknown. The characteristics of Mincle signalling expression in CD patients and experimental colitis were examined. The functional role of Mincle signalling in the intestine was addressed in experimental colitis models in vivo by using Mincle knock-out [Mincle-/-] mice. In addition, neutralising anti-Mincle antibody, downstream spleen tyrosine kinase [Syk] inhibitor, and Mincle pharmacological agonist were used to study the Mincle signalling in intestine. Bone marrow-derived macrophages were collected from mice and used to further verify the effect of Mincle signalling in macrophages. This study has shown that Mincle signalling was significantly elevated in active human CD and experimental colitis, and macrophages were the principal leukocyte subset that upregulate Mincle signalling. Mincle deficiency and Syk pharmacological inhibition ameliorated the colitis by reducing induced macrophage pyroptosis, and activation of Mincle with the agonist aggravated the intestinal inflammation. The ex vivo studies demonstrated that activation of Mincle signalling promoted the release of proinflammatory cytokines, whereas its absence restricted release of proinflammatory cytokines from pyroptosis of macrophages. In addition, Mincle/Syk signalling in macrophages could promote the production of chemokines to recruit neutrophils by activating mitogen-activated protein kinase [MAPK] during intestinal inflammation. Mincle signalling promotes intestinal mucosal inflammation by inducing macrophage pyroptosis. Modulation of the Mincle/Syk axis emerges as a potential therapeutic strategy to target inflammation and treat CD.

Sections du résumé

BACKGROUND BACKGROUND
Macrophage-inducible C-type lectin [Mincle] signalling plays a proinflammatory role in different organs such as the brain and liver, but its role in intestinal inflammation, including Crohn's disease [CD], remains unknown.
METHODS METHODS
The characteristics of Mincle signalling expression in CD patients and experimental colitis were examined. The functional role of Mincle signalling in the intestine was addressed in experimental colitis models in vivo by using Mincle knock-out [Mincle-/-] mice. In addition, neutralising anti-Mincle antibody, downstream spleen tyrosine kinase [Syk] inhibitor, and Mincle pharmacological agonist were used to study the Mincle signalling in intestine. Bone marrow-derived macrophages were collected from mice and used to further verify the effect of Mincle signalling in macrophages.
RESULTS RESULTS
This study has shown that Mincle signalling was significantly elevated in active human CD and experimental colitis, and macrophages were the principal leukocyte subset that upregulate Mincle signalling. Mincle deficiency and Syk pharmacological inhibition ameliorated the colitis by reducing induced macrophage pyroptosis, and activation of Mincle with the agonist aggravated the intestinal inflammation. The ex vivo studies demonstrated that activation of Mincle signalling promoted the release of proinflammatory cytokines, whereas its absence restricted release of proinflammatory cytokines from pyroptosis of macrophages. In addition, Mincle/Syk signalling in macrophages could promote the production of chemokines to recruit neutrophils by activating mitogen-activated protein kinase [MAPK] during intestinal inflammation.
CONCLUSIONS CONCLUSIONS
Mincle signalling promotes intestinal mucosal inflammation by inducing macrophage pyroptosis. Modulation of the Mincle/Syk axis emerges as a potential therapeutic strategy to target inflammation and treat CD.

Identifiants

pubmed: 32333776
pii: 5825302
doi: 10.1093/ecco-jcc/jjaa088
doi:

Substances chimiques

CLEC4D protein, human 0
Lectins, C-Type 0
Receptors, Immunologic 0
SYK protein, human EC 2.7.10.2
Syk Kinase EC 2.7.10.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1734-1747

Subventions

Organisme : Distinguished Scholars Foundation of Jiangsu Province
ID : JCRCB2016006
Organisme : Key Project of Science Foundation of the 12th Five-Year Plan
ID : BNJ13J002
Organisme : Innovation Project of Military Medicine
ID : 16CXZ007
Organisme : General Project of Military Logistics Research
ID : CLB19J025

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Wenbin Gong (W)

School of Medicine, Southeast University, Nanjing, P. R. China.
Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Tao Zheng (T)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Kun Guo (K)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Miao Fang (M)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Haohao Xie (H)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Weijie Li (W)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Qinqing Tang (Q)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Zhiwu Hong (Z)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Huajian Ren (H)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Guosheng Gu (G)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Gefei Wang (G)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Xiuwen Wu (X)

Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

Yun Zhao (Y)

Department of General Surgery, BenQ Medical Center, Affiliated BenQ Hospital of Nanjing Medical University, Nanjing, P. R. China.

Jianan Ren (J)

School of Medicine, Southeast University, Nanjing, P. R. China.
Research Institute of General Surgery, Jinling Hospital, Nanjing, P. R. China.

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Classifications MeSH