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人参皂苷Rg1通过调节STAT3信号通路抑制脂多糖诱导的小胶质细胞焦亡

Ginsenoside Rg1 Inhibits Microglia Pyroptosis Induced by Lipopolysaccharide Through Regulating STAT3 Signaling.

作者信息

Yao Yueyi, Li Changyan, Qian Fusheng, Zhao Yu, Shi Xiaoyi, Hong Dan, Ai Qinglong, Zhong Lianmei

机构信息

Science and Technology Achievement Incubation Center, Kunming Medical University, Kunming, 650500, People's Republic of China.

Department of Neurology, First Affiliated Hospital of Kunming Medical University, Kunming, 650032, People's Republic of China.

出版信息

J Inflamm Res. 2021 Dec 7;14:6619-6632. doi: 10.2147/JIR.S326888. eCollection 2021.

Abstract

PURPOSE

Neuroinflammation runs through the whole process of nervous system diseases and brain injury. Inflammasomes are thought to be especially relevant to immune homeostasis, and their dysregulation contributes to pyroptosis. The natural compound Ginsenoside Rg1 has been shown to possess anti-inflammatory effects; however, its underlying mechanisms are not entirely clear. Therefore, this study was undertaken to investigate the role and mechanisms of Rg1 in regulating the production of inflammasomes and pyroptosis of microglia in vivo and in vitro.

METHODS

BV-2 microglial cells were pretreated with Rg1, stattic and interleukin-6 (IL-6), and then stimulated with lipopolysaccharide (LPS) (2μg/mL). Hoechst staining and Annexin V-FITC/PI assay were then carried out. The expression levels of cleaved-caspase-1, pro-caspase-1, interleukin-1β (IL-1β), mature-IL-1β, gasdermin D (GSDMD), activated NH(2)-terminal fragment of GSDMD (GSDMD-N), NOD-, LRR- and pyrin domain-containing 3 (NLRP3), apoptosis-associated speck-like protein containing a CARD (ASC), absent in melanoma 2 (AIM2), signal transducer and activator of transcription 3 (STAT3) and phosphorylated STAT3 in BV-2 were detected by Western blotting. Additionally, immunofluorescence staining was used to determine the expression of NLRP3 and p-STAT3 in postnatal rat brain and BV-2 microglia subjected to LPS stimulation and Rg1 pretreatment. The targets of transcription factor STAT3 were predicted by hTFtarget and chromatin immunoprecipitation (ChIP) was used to confirm the interaction between STAT3 and AIM2.

RESULTS

We showed here that Rg1 effectively inhibited the expression of inflammasomes and microglia pyroptosis induced by LPS. The targets predicted data of Rg1 from Swiss target prediction database showed STAT3 had the highest thresholds of probability score. Rg1 can regulate the phosphorylation of STAT3, which binds to the promoter region of inflammasome AIM2.

CONCLUSION

It is suggested that STAT3 signaling can initiate the transcription activity of AIM2. Rg1 regulates microglia pyroptosis in neuroinflammation induced by LPS through targeting STAT3 signaling.

摘要

目的

神经炎症贯穿于神经系统疾病和脑损伤的全过程。炎性小体被认为与免疫稳态特别相关,其失调会导致细胞焦亡。天然化合物人参皂苷Rg1已被证明具有抗炎作用;然而,其潜在机制尚不完全清楚。因此,本研究旨在探讨Rg1在体内和体外调节小胶质细胞炎性小体产生和细胞焦亡中的作用及机制。

方法

用Rg1、Stattic和白细胞介素-6(IL-6)预处理BV-2小胶质细胞,然后用脂多糖(LPS)(2μg/mL)刺激。随后进行Hoechst染色和Annexin V-FITC/PI检测。通过蛋白质免疫印迹法检测BV-2中裂解的半胱天冬酶-1、前半胱天冬酶-1、白细胞介素-1β(IL-1β)、成熟IL-1β、gasdermin D(GSDMD)、GSDMD活化的氨基末端片段(GSDMD-N)、含核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)、含半胱氨酸的天冬氨酸蛋白水解酶激活和募集结构域的凋亡相关斑点样蛋白(ASC)、黑色素瘤缺乏因子2(AIM2)、信号转导子和转录激活子3(STAT3)以及磷酸化STAT3的表达水平。此外,免疫荧光染色用于确定出生后大鼠脑和经LPS刺激及Rg1预处理的BV-2小胶质细胞中NLRP3和p-STAT3的表达。通过hTFtarget预测转录因子STAT3的靶标,并采用染色质免疫沉淀法(ChIP)确认STAT3与AIM2之间的相互作用。

结果

我们在此表明,Rg1有效抑制LPS诱导的炎性小体表达和小胶质细胞焦亡。来自瑞士靶点预测数据库的Rg1靶点预测数据显示,STAT3的概率得分阈值最高。Rg1可调节STAT3的磷酸化,STAT3与炎性小体AIM2的启动子区域结合。

结论

提示STAT3信号可启动AIM2的转录活性。Rg1通过靶向STAT3信号调节LPS诱导的神经炎症中的小胶质细胞焦亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db44/8665869/e3abaa6e7dc8/JIR-14-6619-g0001.jpg

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