Glycidol induces necroptosis and inflammation through autophagy-necrosome pathway in renal cell and mice

Glycidol is a common food contaminant, and its main target organ is the kidney. However, the mechanism of nephrotoxicity of glycidol has not been fully elucidated. In this paper, we investigated the mechanism of glycidol toxicity in mice kidneys and NRK-52E cells. We found that glycidol exposure induced necroptosis in renal cells through the RIPK1/RIPK3/MLKL pathway. Mechanistically, it was further found that glycidol blocked renal cell autophagy and induced ectopic aggregation of p62. Accumulated p62 recruited RIPK1 and activated downstream RIPK1/RIPK3/MLKL necrosome production. At the same time, the accumulated p62 could also participate in the activation of intracellular NF-κB nuclear transcription factor by interacting with RIPK1 to form a signalling complex, which promoted the secretion of inflammatory factors TNF-α and IL-1β, and induced inflammation in the kidney. Our present study provided a new understanding of the complex mechanism of glycidol on renal injury.

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Publication Details

Journal
The Science of The Total Environment
Published
2025-02-18
DOI
https://doi.org/10.1016/j.scitotenv.2025.178852
Primary Topic
Autophagy in Disease and Therapy
Type
article
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article

Glycidol induces necroptosis and inflammation through autophagy-necrosome pathway in renal cell and mice

Meitong Liu, Yuelin Chen, Xinyu Yao, Hongdi Wei et al.
The Science of The Total Environment
Autophagy in Disease and Therapy
article

Glycidol induces necroptosis and inflammation through autophagy-necrosome pathway in renal cell and mice

Meitong Liu, Yuelin Chen, Xinyu Yao, Hongdi Wei, Shuang Guan, Jing Lu
article en

Abstract

Glycidol is a common food contaminant, and its main target organ is the kidney. However, the mechanism of nephrotoxicity of glycidol has not been fully elucidated. In this paper, we investigated the mechanism of glycidol toxicity in mice kidneys and NRK-52E cells. We found that glycidol exposure induced necroptosis in renal cells through the RIPK1/RIPK3/MLKL pathway. Mechanistically, it was further found that glycidol blocked renal cell autophagy and induced ectopic aggregation of p62. Accumulated p62 recruited RIPK1 and activated downstream RIPK1/RIPK3/MLKL necrosome production. At the same time, the accumulated p62 could also participate in the activation of intracellular NF-κB nuclear transcription factor by interacting with RIPK1 to form a signalling complex, which promoted the secretion of inflammatory factors TNF-α and IL-1β, and induced inflammation in the kidney. Our present study provided a new understanding of the complex mechanism of glycidol on renal injury.

The Science of The Total EnvironmentVol. 968
Jilin University (CN)
Good health and well-being
Openalex Percentile: Top 95%
Autophagy in Disease and Therapy
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