1. TWEAK is an activator of Hippo-YAP signaling protecting against hepatic Ischemia/ reperfusion injury.
- Author
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Tong W, Zhu L, Han P, Bai Y, Wang T, Chen D, Li Z, Chi H, Deng X, Zhang Y, and Shen Z
- Subjects
- Animals, Humans, Mice, Male, Adaptor Proteins, Signal Transducing metabolism, Adaptor Proteins, Signal Transducing genetics, Disease Models, Animal, Organoids metabolism, Transcription Factors metabolism, Transcription Factors genetics, Reperfusion Injury metabolism, Cytokine TWEAK metabolism, Hippo Signaling Pathway, TWEAK Receptor metabolism, TWEAK Receptor genetics, Signal Transduction, Liver metabolism, Liver pathology, Protein Serine-Threonine Kinases metabolism, YAP-Signaling Proteins metabolism, Mice, Inbred C57BL
- Abstract
Hepatic ischemia-reperfusion injury (IRI) represents a formidable complication commonly linked with hemorrhagic shock, liver resection, and transplantation. This study aims to elucidate the role of Tumor Necrosis Factor-like Weak Inducer of Apoptosis (TWEAK) in the pathogenesis of hepatic I/R injury and to delineate the underlying mechanisms involved. Utilizing a hypoxia-reoxygenation model in human liver organoids (HLOs) alongside a murine model of warm ischemia-reperfusion injury, we systematically investigated the interplay between TWEAK, its receptor Fn14, and the HIPPO signaling pathway. Our findings indicate that TWEAK pretreatment significantly mitigates IRI in murine livers as well as hypoxia/reoxygenation injury in HLOs. Notably, administration of adeno-associated virus (AAV) to knock down Fn14 abrogated the protective effects of TWEAK in the murine model. Transcriptome sequencing analysis revealed that the interaction between TWEAK and Fn14 enhances cellular resistance to IRI by activating the HIPPO signaling pathway. Overall, TWEAK emerges as a promising therapeutic target for mitigating hepatic I/R injury, potentially improving outcomes in liver transplantation., (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Published
- 2024
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