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Meteorin‐like protein/METRNL/Interleukin‐41 ameliorates atopic dermatitis‐like inflammation.

Authors :
Huang, Danqi
Liu, Xiuting
Gao, Xun
Choi, Chun Kit
Giglio, Giovanni
Farah, Luay
Leung, Ting‐Fan
Wong, Katie Ching‐Yau
Kan, Lea Ling‐Yu
Chong, Jeffrey Wing‐Heung
Meng, Qing‐Jun
Liao, Jinyue
Cheung, Phyllis Fung‐Yi
Wong, Chun‐Kwok
Source :
Allergy. May2024, p1. 15p. 7 Illustrations.
Publication Year :
2024

Abstract

Background Methods Results Conclusions Meteorin‐like protein (METRNL)/Interleukin‐41 (IL‐41) is a novel immune‐secreted cytokine/myokine involved in several inflammatory diseases. However, how METRNL exerts its regulatory properties on skin inflammation remains elusive. This study aims to elucidate the functionality and regulatory mechanism of METRNL in atopic dermatitis (AD).METRNL levels were determined in skin and serum samples from patients with AD and subsequently verified in the vitamin D3 analogue MC903‐induced AD‐like mice model. The cellular target of METRNL activity was identified by multiplex immunostaining, single‐cell RNA‐seq and RNA‐seq.METRNL was significantly upregulated in lesions and serum of patients with dermatitis compared to healthy controls (p <.05). Following repeated MC903 exposure, AD model mice displayed elevated levels of METRNL in both ears and serum. Administration of recombinant murine METRNL protein (rmMETRNL) ameliorated allergic skin inflammation and hallmarks of AD in mice, whereas blocking of METRNL signaling led to the opposite. METRNL enhanced β‐Catenin activation, limited the expression of Th2‐related molecules that attract the accumulation of Arginase‐1 (Arg1)hi macrophages, dendritic cells, and activated mast cells.METRNL can bind to KIT receptor and subsequently alleviate the allergic inflammation of AD by inhibiting the expansion of immune cells, and downregulating inflammatory gene expression by regulating the level of active WNT pathway molecule β‐Catenin. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01054538
Database :
Academic Search Index
Journal :
Allergy
Publication Type :
Academic Journal
Accession number :
177124675
Full Text :
https://doi.org/10.1111/all.16150