Biochemistry & Molecular Biology, Michigan State University, East Lansing, Michigan, USA; Institute for Integrative Toxicology, Michigan State University, East Lansing, Michigan, USA.
Institute for Integrative Toxicology, Michigan State University, East Lansing, Michigan, USA; Microbiology & Molecular Genetics, Michigan Sptate University, East Lansing, Michigan, USA.
J Biol Chem. 2022 Sep;298(9):102301. doi: 10.1016/j.jbc.2022.102301. Epub 2022 Aug 2.
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is a persistent environmental contaminant that induces diverse biological and toxic effects, including reprogramming intermediate metabolism, mediated by the aryl hydrocarbon receptor. However, the specific reprogramming effects of TCDD are unclear. Here, we performed targeted LC-MS analysis of hepatic extracts from mice gavaged with TCDD. We detected an increase in S-(2-carboxyethyl)-L-cysteine, a conjugate from the spontaneous reaction between the cysteine sulfhydryl group and highly reactive acrylyl-CoA, an intermediate in the cobalamin (Cbl)-independent β-oxidation-like metabolism of propionyl-CoA. TCDD repressed genes in both the canonical Cbl-dependent carboxylase and the alternate Cbl-independent β-oxidation-like pathways as well as inhibited methylmalonyl-CoA mutase (MUT) at lower doses. Moreover, TCDD decreased serum Cbl levels and hepatic cobalt levels while eliciting negligible effects on gene expression associated with Cbl absorption, transport, trafficking, or derivatization to 5'-deoxy-adenosylcobalamin (AdoCbl), the required MUT cofactor. Additionally, TCDD induced the gene encoding aconitate decarboxylase 1 (Acod1), the enzyme responsible for decarboxylation of cis-aconitate to itaconate, and dose-dependently increased itaconate levels in hepatic extracts. Our results indicate MUT inhibition is consistent with itaconate activation to itaconyl-CoA, a MUT suicide inactivator that forms an adduct with adenosylcobalamin. This adduct in turn inhibits MUT activity and reduces Cbl levels. Collectively, these results suggest the decrease in MUT activity is due to Cbl depletion following TCDD treatment, which redirects propionyl-CoA metabolism to the alternate Cbl-independent β-oxidation-like pathway. The resulting hepatic accumulation of acrylyl-CoA likely contributes to TCDD-elicited hepatotoxicity and the multihit progression of steatosis to steatohepatitis with fibrosis.
2,3,7,8-四氯二苯并对二恶英(TCDD)是一种持久性的环境污染物,可通过芳烃受体诱导多种生物和毒性作用,包括中间代谢的重编程。然而,TCDD 的具体重编程作用尚不清楚。在这里,我们对用 TCDD 灌胃的小鼠的肝提取物进行了靶向 LC-MS 分析。我们检测到 S-(2-羧乙基)-L-半胱氨酸的增加,这是半胱氨酸巯基与高反应性丙烯酰辅酶 A 自发反应的产物,丙烯酰辅酶 A 是丙酰辅酶 A 的钴胺素(Cbl)非依赖性β-氧化样代谢的中间产物。TCDD 抑制了经典的 Cbl 依赖性羧化酶和替代的 Cbl 非依赖性β-氧化样途径中的基因,并且在较低剂量下抑制了甲基丙二酰辅酶 A 变位酶(MUT)。此外,TCDD 降低了血清 Cbl 水平和肝钴水平,同时对与 Cbl 吸收、转运、运输或衍生为 5'-脱氧-腺苷钴胺素(AdoCbl)相关的基因表达几乎没有影响,AdoCbl 是所需的 MUT 辅助因子。此外,TCDD 诱导顺乌头酸脱羧酶 1(Acod1)的基因表达,该酶负责顺乌头酸的脱羧生成衣康酸,并且衣康酸水平在肝提取物中呈剂量依赖性增加。我们的结果表明,MUT 抑制与衣康酸的激活一致,衣康酸激活为衣康酰辅酶 A,这是一种 MUT 自杀失活剂,与腺苷钴胺素形成加合物。该加合物反过来抑制 MUT 活性并降低 Cbl 水平。总的来说,这些结果表明 MUT 活性的降低是由于 TCDD 处理后 Cbl 的耗竭,这将丙酰辅酶 A 代谢重定向到替代的 Cbl 非依赖性β-氧化样途径。由此产生的肝丙烯酰辅酶 A 的积累可能导致 TCDD 诱导的肝毒性和脂肪变性向脂肪性肝炎伴纤维化的多打击进展。