Acetylation of lactate dehydrogenase B drives NAFLD progression by impairing lactate clearance

被引:65
|
作者
Wang, Tongxin [1 ,2 ]
Chen, Kai [3 ]
Yao, Weilei [1 ,2 ]
Zheng, Ruilong [4 ]
He, Qiongyu [1 ,2 ]
Xia, Jun [1 ,2 ]
Li, Juan [1 ,2 ]
Shao, Yafei [1 ,2 ]
Zhang, Li [1 ,2 ]
Huang, Lu [1 ,2 ]
Qin, Longshan [1 ,2 ]
Xu, Mingming [1 ,2 ]
Zhang, Zheng [1 ,2 ]
Pan, Dingyu [5 ]
Li, Zhen [5 ]
Huang, Feiruo [1 ,2 ,6 ]
机构
[1] Huazhong Agr Univ, Coll Anim Sci & Technol, Dept Anim Nutr & Feed Sci, Wuhan 430070, Peoples R China
[2] Cooperat Innovat Ctr Sustainable Pig Prod, Wuhan 430070, Peoples R China
[3] Wuhan Univ, Zhongnan Hosp, Dept Anesthesiol, Wuhan 430071, Peoples R China
[4] Wageningen Univ & Res, Dept Anim Sci, Anim Nutr Grp, De Elst 1, NL-6708 WD Wageningen, Netherlands
[5] Wuhan Univ, Zhongnan Hosp, Dept Hepatobiliary & Pancreat Surg, Donghu Rd 169, Wuhan 430071, Peoples R China
[6] Huazhong Agr Univ, Minist Educ, Key Lab Environm Correlat Dietol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
PCAF; LDHB; Acetylation; Hepatic lactate clearance; NAFLD; FATTY LIVER-DISEASE; LYSINE ACETYLATION; OXIDATIVE STRESS; METABOLISM; MICE;
D O I
10.1016/j.jhep.2020.11.028
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Lactate has recently been reported to accumulate in the livers of patients progressing from simple steatosis to non-alcoholic steatohepatitis (NASH). However, the underlying mechanism(s) of lactate accumulation and the role of lactate in the progression of non-alcoholic fatty liver disease (NAFLD) are essentially unknown. Methods: We compared the acetylome in liver samples taken from healthy individuals, patients with simple steatosis and patients with NASH to identify potential targets of acetylation with a role in lactate metabolism. Interactions between the acetylated target and acetyltransferases were measured in multiple cell lines. An acetyltransferase inhibitor was injected into high-fat diet (HFD)-fed mice to determine the role of lactate on NAFLD progression in vivo. Results: Hyperacetylation of lactate dehydrogenase B (LDHB) was found to be associated with lactate accumulation in NAFL and NASH livers in humans and mice. P300/CBP-associated factor (PCAF)-mediated acetylation of LDHB K82 was found to significantly decrease LDHB activity and impair hepatic lactate clearance, resulting in lactate accumulation. Acetylated LDHB induced lactate accumulation which exacerbated lipid deposition and inflammatory responses by activating histone hyperacetylation in HFD-induced NASH. The administration of embelin, a PCAF inhibitor, and the generation of an acetylation-deficient mutant of LDHB ameliorated NASH. Conclusion: PCAF-dependent LDHB acetylation plays a key role in hepatic lipid accumulation and inflammatory responses by impairing lactate clearance; this process might be a potential therapeutic target for the treatment of NASH. Lay summary: Lactate is known to accumulate in the livers of patients during the progression of non-alcoholic fatty liver disease (NAFLD); however, the underlying mechanism(s) of this accumulation and its importance in disease progression are unknown. Herein, we show that the acetylation of an enzyme involved in lactate metabolism leads to impaired lactate clearance and exacerbates NAFLD progression. (C) 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1038 / 1052
页数:15
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