ZHX2 emerges as a negative regulator of mitochondrial oxidative phosphorylation during acute liver injury

Yankun Zhang, Yuchen Fan, Huili Hu, Xiaohui Zhang, Zehua Wang, Zhuanchang Wu, Liyuan Wang, Xiangguo Yu, Xiaojia Song, Peng Xiang, Xiaodong Zhang, Tixiao Wang, Siyu Tan, Chunyang Li, Lifen Gao, Xiaohong Liang, Shuijie Li, Nailin Li, Xuetian Yue () and Chunhong Ma ()
Additional contact information
Yankun Zhang: Cheeloo Medical College of Shandong University
Yuchen Fan: Qilu Hospital of Shandong University
Huili Hu: Shandong University
Xiaohui Zhang: Shandong University
Zehua Wang: Cheeloo Medical College of Shandong University
Zhuanchang Wu: Cheeloo Medical College of Shandong University
Liyuan Wang: Cheeloo Medical College of Shandong University
Xiangguo Yu: Cheeloo Medical College of Shandong University
Xiaojia Song: Cheeloo Medical College of Shandong University
Peng Xiang: Cheeloo Medical College of Shandong University
Xiaodong Zhang: Cheeloo Medical College of Shandong University
Tixiao Wang: Cheeloo Medical College of Shandong University
Siyu Tan: Cheeloo Medical College of Shandong University
Chunyang Li: Cheeloo Medical College of Shandong University
Lifen Gao: Cheeloo Medical College of Shandong University
Xiaohong Liang: Cheeloo Medical College of Shandong University
Shuijie Li: Harbin Medical University
Nailin Li: Karolinska Institute
Xuetian Yue: Cheeloo Medical College of Shandong University
Chunhong Ma: Cheeloo Medical College of Shandong University

Nature Communications, 2023, vol. 14, issue 1, 1-18

Abstract: Abstract Mitochondria dysfunction contributes to acute liver injuries, and mitochondrial regulators, such as PGC-1α and MCJ, affect liver regeneration. Therefore, identification of mitochondrial modulators may pave the way for developing therapeutic strategies. Here, ZHX2 is identified as a mitochondrial regulator during acute liver injury. ZHX2 both transcriptionally inhibits expression of several mitochondrial electron transport chain genes and decreases PGC-1α stability, leading to reduction of mitochondrial mass and OXPHOS. Loss of Zhx2 promotes liver recovery by increasing mitochondrial OXPHOS in mice with partial hepatectomy or CCl4-induced liver injury, and inhibition of PGC-1α or electron transport chain abolishes these effects. Notably, ZHX2 expression is higher in liver tissues from patients with drug-induced liver injury and is negatively correlated with mitochondrial mass marker TOM20. Delivery of shRNA targeting Zhx2 effectively protects mice from CCl4-induced liver injury. Together, our data clarify ZHX2 as a negative regulator of mitochondrial OXPHOS and a potential target for developing strategies for improving liver recovery after acute injuries.

Date: 2023
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DOI: 10.1038/s41467-023-43439-0

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