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丹参酮 IIA 通过调节氧化还原平衡和谷氨酰胺代谢激活核因子红细胞 2 相关因子 2 抑制肺纤维化。

Tanshinone IIA Activates Nuclear Factor-Erythroid 2-Related Factor 2 to Restrain Pulmonary Fibrosis via Regulation of Redox Homeostasis and Glutaminolysis.

机构信息

State Key Laboratory of Natural Medicines, Department of Pharmacognosy, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China.

出版信息

Antioxid Redox Signal. 2019 May 20;30(15):1831-1848. doi: 10.1089/ars.2018.7569. Epub 2018 Sep 22.

Abstract

AIMS

Pulmonary fibrosis (PF) is characterized by myofibroblast activation through oxidative stress. However, the precise regulation of myofibroblast transdifferentiation remains largely uncharacterized.

RESULTS

In this study, we found that tanshinone IIA (Tan-IIA), an active component in the root of Salvia miltiorrhiza Bunge, can suppress reactive oxygen species (ROS)-mediated activation of myofibroblast and reduce extracellular matrix deposition in bleomycin (BLM)-challenged mice through the regulation of nuclear factor-erythroid 2-related factor 2 (Nrf2). Additionally, Tan-IIA restored redox homeostasis by upregulating Nrf2 with NADPH oxidase 4 suppression and effectively prevented myofibroblast activation by blocking ROS-mediated protein kinase C delta (PKCδ)/Smad3 signaling. Nrf2 knockdown in the fibroblasts and the lungs of BLM-treated mice reduced the inhibitory effects of Tan-IIA, indicating the essential role of Nrf2 in the Tan-IIA activity. Tan-IIA impaired the binding of kelch-like ECH-associated protein 1 (Keap1) to Nrf2 by promoting the degradation of Keap1 and thereby increasing Nrf2 induction by protecting Nrf2 stability against ubiquitination and proteasomal degradation. Importantly, we also found that the glutamate anaplerotic pathway was involved in energy generation and biosynthesis in activated myofibroblasts and their proliferation. Tan-IIA shunted glutaminolysis into glutathione (GSH) production by activating Nrf2, resulting in the reduction of glutamate availability for tricarboxylic acid cycle. Ultimately, myofibroblast activation was prevented by impairing cell proliferation. Innovation and Conclusion: In addition to the regulation of redox homeostasis, our work showed that Tan-IIA activated Nrf2/GSH signaling pathway to limit glutaminolysis in myofibroblast proliferation, which provided further insight into the critical function of Nrf2 in PF.

摘要

目的

肺纤维化(PF)的特征是肌成纤维细胞通过氧化应激激活。然而,肌成纤维细胞转分化的确切调节仍很大程度上未被描述。

结果

在这项研究中,我们发现丹参酮 IIA(Tan-IIA),丹参根部的一种活性成分,可以通过调节核因子-红细胞 2 相关因子 2(Nrf2)抑制活性氧(ROS)介导的肌成纤维细胞激活,并减少博莱霉素(BLM)挑战的小鼠细胞外基质沉积。此外,Tan-IIA 通过抑制 NADPH 氧化酶 4 和上调 Nrf2 来恢复氧化还原平衡,有效阻止 ROS 介导的蛋白激酶 C 德尔塔(PKCδ)/Smad3 信号转导,从而阻止肌成纤维细胞激活。在 BLM 处理的小鼠成纤维细胞和肺中的 Nrf2 敲低降低了 Tan-IIA 的抑制作用,表明 Nrf2 在 Tan-IIA 活性中起关键作用。Tan-IIA 通过促进 Keap1 的降解,破坏 Kelch 样 ECH 相关蛋白 1(Keap1)与 Nrf2 的结合,从而通过保护 Nrf2 稳定性防止泛素化和蛋白酶体降解来增加 Nrf2 的诱导,从而损害 Keap1 与 Nrf2 的结合,从而增加 Nrf2 的诱导。重要的是,我们还发现谷氨酸氨酰基途径参与了激活的肌成纤维细胞及其增殖中的能量产生和生物合成。Tan-IIA 通过激活 Nrf2 将谷氨酰胺分解为谷胱甘肽(GSH),从而减少三羧酸循环中谷氨酸的可用性。最终,通过损害细胞增殖来阻止肌成纤维细胞的激活。

创新和结论

除了调节氧化还原平衡外,我们的工作还表明,Tan-IIA 激活了 Nrf2/GSH 信号通路,限制了肌成纤维细胞增殖中的谷氨酰胺分解,这为 Nrf2 在 PF 中的关键功能提供了进一步的见解。

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