Piezo2 + mechanosensory neurons and glial cells initiate resident macrophage activation in postoperative ileus

炎症 免疫染色 病理 CXCL10型 下调和上调 巨噬细胞 医学 趋化因子 机械敏感通道 生物 免疫学 运动性 细胞生物学 体内 小胶质细胞 肠梗阻 细胞 胶质纤维酸性蛋白 体外 肠神经系统 CXCL2型 免疫组织化学 神经胶质 小肠
作者
Zheng Wang,Elodie Modave,Samuel Van Remoortel,Nika Pajk,Pieter Vanden Berghe,Yifan Chen,Marte Vandeput,Iris Appeltans,Runze Quan,Gianluca Matteoli,Nathalie Stakenborg,Guy E. Boeckxstaens
出处
期刊:Gut [BMJ]
卷期号:: gutjnl-2025
标识
DOI:10.1136/gutjnl-2025-336369
摘要

Background Postoperative ileus (POI) is a common complication of abdominal surgery and is marked by impaired gut motility driven by inflammation of the muscularis externa. While muscularis macrophages (mMfs) are central to this response, the early trigger(s) responsible for their activation remain unclear. Objective To assess the role of the mechanosensitive neurons and enteric glial cells (EGCs) in the early activation of mMfs in POI. Design Intestinal manipulation (IM) was performed in wild-type C57BL/6 mice and the kinetics of cell influx and activation were assessed. Single-nucleus RNA sequencing (snRNA-seq) was conducted on the intestinal muscularis layer 30 min after sham and IM. In vitro and in vivo studies were conducted to validate the role of Ccl4 and Cxcl10 in mMf activation. D-GsMTx4 was administered while Wnt1 Cre ; Piezo2 fl/wt mice were generated to analyse the role of Piezo2 in POI. Results Inflammatory cells, primarily mature mMfs, increased in the muscularis externa within 30 min post-IM due to cell proliferation, while cFos staining showed enteric neurons and EGCs to be activated prior to mMfs. Immunostaining revealed expression of Piezo2 in the enteric neurons and EGCs and inhibition of Piezo2 significantly reduced IM-induced inflammation. snRNAseq indicated cell-cell communication between mMfs and mMfs/EGCs via the release of Ccl4 and Cxcl10, respectively. Finally, blockade of Ccl4 and Cxcl10 attenuated mMf activation. Conclusions Our findings reveal activation of Piezo2-expressing enteric neurons and EGCs as a very early step in IM-induced inflammation of POI. These cells subsequently activate mMfs resulting in upregulation of Ccl4, further amplifying the inflammatory cascade. These results highlight a key role for Piezo2 in the pathophysiology of POI.
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