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Cystathionine gamma-lyase (Cth) induces efferocytosis in macrophages via ERK1/2 to modulate intestinal barrier repair.

Authors :
Zhao, Xiao-Hu
Yang, Ting
Zheng, Meng-Yao
Zhao, Peinan
An, Li-Ya
Qi, Yu-Xing
Yi, Ke-Qian
Zhang, Peng-Cheng
Sun, Da-Li
Source :
Cell Communication & Signaling. 1/23/2023, Vol. 21 Issue 1, p1-20. 20p.
Publication Year :
2023

Abstract

Background: The inflammatory response induced by intestinal ischaemia‒reperfusion injury (I/R) is closely associated with infectious complications and mortality in critically ill patients, and the timely and effective clearance of apoptotic cells is an important part of reducing the inflammatory response. Studies have shown that the efferocytosis by phagocytes plays an important role. Recently, studies using small intestine organoid models showed that macrophage efferocytosis could promote the repair capacity of the intestinal epithelium. However, no studies have reported efferocytosis in the repair of I/R in animal models. Results: We used an in vivo efferocytosis assay and discovered that macrophage efferocytosis played an indispensable role in repairing and maintaining intestinal barrier function after I/R. In addition, the specific molecular mechanism that induced macrophage efferocytosis was Cth-ERK1/2 dependent. We found that Cth drove macrophage efferocytosis in vivo and in vitro. Overexpression/silencing Cth promoted/inhibited the ERK1/2 pathway, respectively, which in turn affected efferocytosis and mediated intestinal barrier recovery. In addition, we found that the levels of Cth and macrophage efferocytosis were positively correlated with the recovery of intestinal function in clinical patients. Conclusion: Cth can activate the ERK1/2 signalling pathway, induce macrophage efferocytosis, and thus promote intestinal barrier repair. ANik3mFzVX11c2tZJFb62z Video Abstract [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1478811X
Volume :
21
Issue :
1
Database :
Academic Search Index
Journal :
Cell Communication & Signaling
Publication Type :
Academic Journal
Accession number :
161448499
Full Text :
https://doi.org/10.1186/s12964-022-01030-y