4.8 Article

Zn Induces Lipophagy via the Deacetylation of Beclin1 and Alleviates Cu-Induced Lipotoxicity at Their Environmentally Relevant Concentrations

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 8, Pages 4943-4953

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c08609

Keywords

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Funding

  1. National Natural Science Foundation of China [32030111, 31872585]
  2. National Key R&D Program of China [2018YFD0900600]

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This study found that Zn activated lipophagy, alleviating Cu-induced lipid accumulation by promoting deacetylation of Beclin1. This previously unidentified mechanism sheds light on the antagonistic effects of Cu and Zn on metabolism at environmentally relevant concentrations. The importance of combined exposure and the role of Beclin1 deacetylation in promoting lipophagy were highlighted in understanding the biological effects of heavy metals during environmental risk assessments.
In this study, the mechanisms of environmentally relevant doses of Cu and Zn mixtures influencing lipid deposition and metabolism were investigated in freshwater teleost yellow catfish Pelteobagrus fulvidraco (2 months old, 4.95 (t0.01 g, mean +/- SEM). Our study indicated that waterborne Cu exposure increased lipid content, while Zn activated lipophagic flux and alleviated Cu-induced lipid accumulation. Yellow catfish hepatocytes treated with Zn or Zn + Cu activated autophagy-specific lipophagy, decreased lipid storage, and increased nonesterified fatty acid (NEFA) release, suggesting a causal relationship between lipophagy and lipid droplet (LD) breakdown under Zn and Zn + Cu conditions. Our further investigation found that Beclin1 deacetylation by sirtuin 1 (SIRT1) was required for Zn- and Zn + Cu-induced lipophagy and lipolysis, and lysine residues 427 and 434 were key sites for Beclin1 deacetylation. Taken together, these findings show that the Zn-induced deacetylation of Beclin1 promotes lipophagy as an important pathway to alleviate Cu-induced lipid accumulation in fish, which reveals a previously unidentified mechanism for understanding the antagonistic effects of Cu and Zn on metabolism at their environmentally relevant concentrations. Our results highlight the importance of combined exposure when the biological effects of heavy metals are evaluated during environmental risk assessments.

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