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在肝损伤期间,丝裂原活化蛋白激酶13(MAPK13)使磷酸甘油酸脱氢酶(PHGDH)磷酸化,并通过伴侣介导的自噬促进其降解。

MAPK13 phosphorylates PHGDH and promotes its degradation via chaperone-mediated autophagy during liver injury.

作者信息

Xing Ru, Liu Ruilong, Man Yongxiao, Liu Chen, Zhang Yajuan, Gao Hong, Yang Weiwei

机构信息

Key Laboratory of Multi-cell Systems, Shanghai Key Laboratory of Molecular Andrology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.

Ben May Department for Cancer Research, The University of Chicago, Chicago, IL, USA.

出版信息

Cell Discov. 2025 Feb 18;11(1):15. doi: 10.1038/s41421-024-00758-w.

Abstract

Drug-induced liver injury (DILI) is the leading cause of acute liver failure and poses a significant clinical challenge in both diagnosis and treatment. Serine synthesis pathway (SSP) links glycolysis to one-carbon cycle and plays an important role in cell homeostasis by regulating substance synthesis, redox homeostasis and gene expression. However, the regulatory mechanism of SSP in DILI remains unclear. Phosphoglycerate dehydrogenase (PHGDH) is the rate-limiting enzyme in SSP. Here we show that during DILI, mitogen-activated protein kinase 13 (MAPK13) is activated and then phosphorylates PHGDH at serine 371 upon oxidative stress, which triggers PHGDH protein degradation via chaperone-mediated autophagy (CMA) pathway. PHGDH degradation suppresses SSP and glutathione production, thereby exacerbating DILI and cholestatic liver injury. Importantly, both MAPK13 inhibition and dietary serine supplementation ameliorates these liver injuries. Our finding demonstrates a unique regulatory mechanism of SSP, in which MAPK13 phosphorylates PHGDH and promotes its CMA degradation, establishes its critical role in DILI and cholestatic liver injury, and highlights the therapeutic potential of MAPK13 inhibitor or dietary serine to treat these liver injuries.

摘要

药物性肝损伤(DILI)是急性肝衰竭的主要原因,在诊断和治疗方面均构成重大临床挑战。丝氨酸合成途径(SSP)将糖酵解与一碳循环相连接,并通过调节物质合成、氧化还原稳态和基因表达在细胞内稳态中发挥重要作用。然而,SSP在DILI中的调控机制仍不清楚。磷酸甘油酸脱氢酶(PHGDH)是SSP中的限速酶。在此我们表明,在DILI过程中,丝裂原活化蛋白激酶13(MAPK13)被激活,然后在氧化应激时使PHGDH的丝氨酸371位点磷酸化,这通过伴侣介导的自噬(CMA)途径触发PHGDH蛋白降解。PHGDH降解会抑制SSP和谷胱甘肽生成,从而加重DILI和胆汁淤积性肝损伤。重要的是,抑制MAPK13和补充膳食丝氨酸均可改善这些肝损伤。我们的研究发现揭示了SSP一种独特的调控机制,即MAPK13使PHGDH磷酸化并促进其CMA降解,确定了其在DILI和胆汁淤积性肝损伤中的关键作用,并突出了MAPK13抑制剂或膳食丝氨酸治疗这些肝损伤的潜在治疗价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc3/11832932/f03c61420f06/41421_2024_758_Fig1_HTML.jpg

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