Extracellular vesicles containing GAS6 protect the liver from ischemia-reperfusion injury by enhancing macrophage efferocytosis via MerTK-ERK-COX2 signaling

• Published in: Cell death discovery 2024-09, Vol.10 (1), p.401-13, Article 401
• Main Authors: Miao, Longyu, Yu, Chaoqun, Guan, Ge, Luan, Xiaoyu, Jin, Xiaoshuang, Pan, Meiqi, Yang, Yuzhen, Yan, Jiaoyang, Chen, Peng, Di, Guohu
• Format: Article
• Language: English
• Subjects: 631/337/475/2290; 631/532/2074; 692/699/1503/1607/1605; Apoptosis; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Cycle Analysis; Cyclooxygenase-2; Extracellular signal-regulated kinase; Extracellular vesicles; Hepatocytes; Inflammation; Ischemia; Kinases; Life Sciences; Liver; Liver transplantation; Macrophages; Mesenchymal stem cells; Phenotypes; Proteomics; Reperfusion; Signal transduction; Stem cell transplantation; Stem Cells; Transfection
• ISSN: 2058-7716; 2058-7716
• DOI: 10.1038/s41420-024-02169-y

Hepatic ischemia-reperfusion injury (HIRI) is a significant issue during liver transplantation and surgery, contributing to the liver failure or even mortality. Although extracellular vesicles derived from mesenchymal stem cells (MSC-EVs) have shown substantial potentials in cell replacement therapy of various organ ischemia reperfusion injuries (IRIs), the precise mechanisms remain unclear. In this study, we demonstrate that systemic MSC-EVs administration is predominantly absorbed by macrophages, and verified that it could significantly reduce the liver injury and inflammatory response in mice suffering from HIRI. Furthermore, treatment with MSC-EVs induces macrophage polarization toward an anti-inflammatory phenotype. Mechanistically, proteomic profiling reveals an enrichment of growth arrest-specific 6 (GAS6) in MSC-EVs, significantly promoting the activation of myeloid-epithelial-reproductive tyrosine kinase/extracellular regulated protein kinases/cyclooxygenase 2 (MerTK/ERK/COX2) signaling pathway in macrophages and further enhancing their efferocytosis efficiency. Knockdown of GAS6 via lentiviral transfection or inhibition of MerTK using UNC2025 (a MerTK small molecule inhibitor) partially eliminates the protective effects of MSC-EVs on macrophage efferocytosis and liver injury. Overall, our findings support that MSC-EVs enriched GAS6 execute an anti-inflammation effect, highlighting that treatment based on the modulation of macrophage function by MSC-EVs as a promising approach in IRI. HIRI is a thorny problem after liver surgery such as liver transplantation. In a murine model of HIRI, MSC-EVs enriched GAS6 effectively enhance macrophage efferocytosis both in vivo and in vitro through the GAS6/MerTK/ERK/COX2 signaling pathway and significantly mitigate liver injury. This image was drawn by the authors.