Swainsonine inhibits autophagic degradation and causes cytotoxicity by reducing CTSD O-GlcNAcylation

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemico-Biological Interactions Pub Date : 2023-09-01 DOI:10.1016/j.cbi.2023.110629
Shuai Wang , Panpan Tan , Hongwei Wang , Jicang Wang , Cai Zhang , Hao Lu , Baoyu Zhao
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Abstract

Swainsonine (SW) is the primary toxin in locoweed, a poisonous plant. SW can cause animal poisoning, affect the quality and safety of meat products and threaten human health, but the mechanism of its toxicity is little defined. Here, we identified 159 differentially expressed proteins, many of which are involved in autophagy and glycosylation modification processes, using proteomics sequencing analysis. O-linked-N-acetylglucosamylation (O-GlcNAcylation) is a glycosylation modification widely involved in various biological processes. Our results show that SW toxicity is related to O-GlcNAcylation. In addition, increased O-GlcNAcylation with the O-GlcNAcase (OGA) inhibitor TMG promoted autophagy, while decreased O-GlcNAcylation with the O-GlcNAc transferase (OGT) inhibitor OSMI inhibited autophagy. Further analysis by Immunoprecipitation (IP) showed that SW could change the O-GlcNAcylation of Cathepsin D (CTSD), reducing the expression of mature CTSD (m-CTSD). In summary, these findings suggest that SW inhibits the O-GlcNAcylation of CTSD, affecting its maturation and leading to the impairment of lysosome function. Consequently, it inhibits autophagy degradation, and causes cytotoxicity, providing a new theoretical basis for SW toxicological mechanism.

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苦马豆素抑制自噬降解并通过降低CTSD o - glcn酰化引起细胞毒性
马豆素(Swainsonine, SW)是一种有毒植物麻草中的主要毒素。SW可引起动物中毒,影响肉制品质量安全,威胁人类健康,但其毒性机制尚不明确。在这里,我们鉴定了159个差异表达蛋白,其中许多参与自噬和糖基化修饰过程,使用蛋白质组学测序分析。O-linked-N-acetylglucosamylation (o - glcnac酰化)是一种广泛参与多种生物过程的糖基化修饰。我们的研究结果表明,SW毒性与o - glcn酰化有关。此外,与O-GlcNAcase (OGA)抑制剂TMG的o - glcnac酰化升高可促进自噬,而与O-GlcNAcase转移酶(OGT)抑制剂OSMI的o - glcnac酰化降低可抑制自噬。免疫沉淀(IP)进一步分析表明,SW可以改变组织蛋白酶D (CTSD)的o - glcn酰化,降低成熟CTSD (m-CTSD)的表达。综上所述,这些发现表明,SW抑制CTSD的o - glcn酰化,影响其成熟,导致溶酶体功能受损。从而抑制自噬降解,引起细胞毒性,为研究SW毒理学机制提供了新的理论依据。
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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