TRIM21 介导的 SQSTM1/p62 泛素化可消除其 Ser403 磷酸化并增强棕榈酸的细胞毒性。

Peng Yang, Shenglan Gao, Jianliang Shen, Tong Liu, Kevin Lu, Xinlu Han, Jun Wang, Hong-Min Ni, Wen-Xing Ding, Hong Li, Ji-An Pan, Kesong Peng, Wei-Xing Zong
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The ubiquitin E3 ligase TRIM21 ubiquitinates SQSTM1 at the K7 residue and abolishes the PB1 dimerization, S403 phosphorylation, and SQSTM1 aggregation. TRIM21 is oxidized at C92, C111, and C114 to form disulfide bonds that lead to its oligomerization and decreased E3 activity. Mutagenizing the three C residues to S (3CS) abolishes TRIM21 oligomerization and increases its E3 activity. TRIM21 ablation leads to decreased SQSTM1 K7 ubiquitination, hence elevated SQSTM1 S403 phosphorylation and aggregation, which confers protection against PA-induced oxidative stress and cytotoxicity. Therefore, TRIM21 is a negative regulator of SQSTM1 phosphorylation, aggregation, and the antioxidant sequestration function. TRIM21 is oxidized to reduce its E3 activity that helps enhance the SQSTM1-KEAP1-NFE2L2 antioxidant pathway. 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引用次数: 0

摘要

长链游离脂肪酸(FFAs)的积累和氧化毒性是导致多种病症的主要原因。游离脂肪酸的细胞毒性机制仍然难以捉摸。在这里,我们发现棕榈酸(PA)--循环中最丰富的游离脂肪酸--会诱导 SQSTM1/p62(序列组 1)的 S403 磷酸化及其聚集,从而封存 KEAP1 并激活非经典的 SQSTM1-KEAP1-NFE2L2 抗氧化途径。PA 诱导的 SQSTM1 S403 磷酸化和聚集依赖于 SQSTM1 K7-D69 氢键的形成以及 Phox 和 Bem1(PB1)结构域的二聚化,这有利于 TBK1 的招募,从而使 SQSTM1 S403 磷酸化。泛素 E3 连接酶 TRIM21 可在 K7 残基上泛素化 SQSTM1,从而消除 PB1 的二聚化、S403 磷酸化和 SQSTM1 的聚集。TRIM21 在 C92、C111 和 C114 处被氧化,形成二硫键,导致其寡聚化和 E3 活性降低。将三个 C 残基突变为 S(3CS)可消除 TRIM21 的低聚作用并提高其 E3 活性。TRIM21 消减会导致 SQSTM1 K7 泛素化减少,从而使 SQSTM1 S403 磷酸化和聚集增加,从而使其免受 PA 诱导的氧化应激和细胞毒性的影响。因此,TRIM21 是 SQSTM1 磷酸化、聚集和抗氧化螯合功能的负调控因子。TRIM21 被氧化后会降低其 E3 活性,从而有助于增强 SQSTM1-KEAP1-NFE2L2 的抗氧化途径。抑制 TRIM21 可能是保护组织免受长链脂肪酸导致的脂毒性的一种可行策略。
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TRIM21-mediated ubiquitination of SQSTM1/p62 abolishes its Ser403 phosphorylation and enhances palmitic acid cytotoxicity.

Long-chain free fatty acids (FFAs) accumulation and oxidative toxicity is a major cause for several pathological conditions. The mechanisms underlying FFA cytotoxicity remain elusive. Here we show that palmitic acid (PA), the most abundant FFA in the circulation, induces S403 phosphorylation of SQSTM1/p62 (sequestosome 1) and its aggregation, which sequesters KEAP1 and activates the non-canonical SQSTM1-KEAP1-NFE2L2 antioxidant pathway. The PA-induced SQSTM1 S403 phosphorylation and aggregation are dependent on SQSTM1 K7-D69 hydrogen bond formation and dimerization in the Phox and Bem1 (PB1) domain, which facilitates the recruitment of TBK1 that phosphorylates SQSTM1 S403. The ubiquitin E3 ligase TRIM21 ubiquitinates SQSTM1 at the K7 residue and abolishes the PB1 dimerization, S403 phosphorylation, and SQSTM1 aggregation. TRIM21 is oxidized at C92, C111, and C114 to form disulfide bonds that lead to its oligomerization and decreased E3 activity. Mutagenizing the three C residues to S (3CS) abolishes TRIM21 oligomerization and increases its E3 activity. TRIM21 ablation leads to decreased SQSTM1 K7 ubiquitination, hence elevated SQSTM1 S403 phosphorylation and aggregation, which confers protection against PA-induced oxidative stress and cytotoxicity. Therefore, TRIM21 is a negative regulator of SQSTM1 phosphorylation, aggregation, and the antioxidant sequestration function. TRIM21 is oxidized to reduce its E3 activity that helps enhance the SQSTM1-KEAP1-NFE2L2 antioxidant pathway. Inhibition of TRIM21 May be a viable strategy to protect tissues from lipotoxicity resulting from long-chain FFAs.Abbreviations: ER: endoplasmic reticulum; FFA: free fatty acid; HMOX1/HO-1: heme oxygenase 1; IB: immunoblotting; IF: immunofluorescence; IP: immunoprecipitation; KEAP1: kelch like ECH associated protein 1; MASH: metabolic dysfunction-associated steatohepatitis; MEF: mouse embryonic fibroblast; NFE2L2/Nrf2: NFE2 like BZIP transcription factor 2; PA: palmitic acid; PB1: Phox and Bem 1; ROS: reactive oxygen species; SLD: steatotic liver disease; SQSTM1: sequestosome 1; TBK1: TANK-binding kinase 1; TRIM21: tripartite motif containing 21.

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