Inhibition of PGK1 ameliorates acute kidney injury through inactivating the PKM2/ALOX12/ferroptosis pathway in a study with male mice

Despite decades of studies into the mechanisms underlying acute kidney injury (AKI), the effective clinical therapies are still limited. Here we report that the development of AKI was attenuated by conditional knockout of phosphoglycerate kinase 1 (PGK1) in renal tubular epithelial cells (RTECs) and aggravated by specific overexpression of PGK1 and administration of 3-phosphoglycerate (3-PG) in male mice. PGK1 interacted with pyruvate kinase M2 (PKM2), inducing PKM2 phosphorylation, promoting the formation of the PKM2 dimer and the subsequent nuclear translocation of PKM2. In the nucleus, the interaction of PKM2 with Pknox1 potentiated the enrichment of Pknox1 within ALOX12 promoters, which resulted in ALOX12-mediated ferroptosis in RTECs. Our drug screening experiments identified L7DG as a potential PGK1 inhibitor which exhibited protective effects against ischemic/reperfusion (I/R)-induced renal injury. Overall, we establish that genetic and pharmacological inhibition of PGK1 might be proposed as an avenue for managing AKI.

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Publication Details

Journal
Nature Communications
Published
2025-10-24
DOI
https://doi.org/10.1038/s41467-025-64480-1
Citations
2
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
3.04

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article

Inhibition of PGK1 ameliorates acute kidney injury through inactivating the PKM2/ALOX12/ferroptosis pathway in a study with male mice

Mengyuan Wang, Zhengyang Bao, Yanling Wei, Yuanyuan Wen et al.
2 citations
Nature Communications
Ferroptosis and cancer prognosis
3.04
article

Inhibition of PGK1 ameliorates acute kidney injury through inactivating the PKM2/ALOX12/ferroptosis pathway in a study with male mice

Mengyuan Wang, Zhengyang Bao, Yanling Wei, Yuanyuan Wen, Xinyu Meng, Neng Bao, Chenyang Zhao, Qing-Bo Lu, Xuexue Zhu, Hai‐Jian Sun, Na Li, Jia‐Bao Su, Xiao Fu, Ao-Yuan Zhang, Guo Chen, Le-Ming Ji, An‐Jing Xu
article en
2 citations

Abstract

Despite decades of studies into the mechanisms underlying acute kidney injury (AKI), the effective clinical therapies are still limited. Here we report that the development of AKI was attenuated by conditional knockout of phosphoglycerate kinase 1 (PGK1) in renal tubular epithelial cells (RTECs) and aggravated by specific overexpression of PGK1 and administration of 3-phosphoglycerate (3-PG) in male mice. PGK1 interacted with pyruvate kinase M2 (PKM2), inducing PKM2 phosphorylation, promoting the formation of the PKM2 dimer and the subsequent nuclear translocation of PKM2. In the nucleus, the interaction of PKM2 with Pknox1 potentiated the enrichment of Pknox1 within ALOX12 promoters, which resulted in ALOX12-mediated ferroptosis in RTECs. Our drug screening experiments identified L7DG as a potential PGK1 inhibitor which exhibited protective effects against ischemic/reperfusion (I/R)-induced renal injury. Overall, we establish that genetic and pharmacological inhibition of PGK1 might be proposed as an avenue for managing AKI.

Nature CommunicationsVol. 16(1)
Jiangnan University (CN), China Pharmaceutical University (CN), Jiangxi Maternal and Child Health Hospital (CN), Wuxi Fourth People's Hospital (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Jiangnan University, Natural Science Foundation of Jiangsu Province, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 7%
Ferroptosis and cancer prognosis
3.04
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