Author:
Wang Jin,Kang Haixia,Zhao Wenying,Bai Wenjuan,Qi Xin,Yan Kepeng,Miao Naijun,Dong Dong,Wang Yuanyuan,Thanabalasuriar Ajitha,Zhang Dachuan,Ye Youqiong,Xu Tian-le,Li Bin,Wang Jing
Abstract
AbstractNeutrophils are the most abundant immune cells that constantly patrol and marginate into the vascular beds of multiple tissues to support immune homeostasis. The extent to which neutrophils undergo adaptation in response to diverse tissue microenvironments, and the resultant biological implications of such adaptation, remains unclear. Here, we performed intravital imaging, transcriptional, and functional analyses of neutrophils in different tissues. Our findings showed that the lung harbors a transcriptionally distinct neutrophil population with unique migratory behaviors. These resident-like neutrophils guarantee a rapid response upon infection and play an important role in maintaining the homeostasis of pulmonary vasculature. Notably, pulmonary neutrophils are imprinted by mechanical cues via the mechanosensitive ion channel Piezo1. Mice with conditional Piezo1 ablation lost lung-specific neutrophil signatures, and showed impaired lung capillary angiogenesis. Furthermore, these mice displayed increased susceptibility to airway infection. Collectively, these data identify mechanical sensing via Piezo1 as an important driver for tissue-specialized neutrophils that support pulmonary homeostasis.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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