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黄芩苷通过阻断巨噬细胞中的线粒体Z-DNA形成和ZBP1-PAN凋亡小体组装来抑制PAN凋亡。

Baicalin inhibits PANoptosis by blocking mitochondrial Z-DNA formation and ZBP1-PANoptosome assembly in macrophages.

作者信息

You Yi-Ping, Yan Liang, Ke Hua-Yu, Li Ya-Ping, Shi Zi-Jian, Zhou Zhi-Ya, Yang Hai-Yan, Yuan Tao, Gan Ying-Qing, Lu Na, Xu Li-Hui, Hu Bo, Ou-Yang Dong-Yun, Zha Qing-Bing, He Xian-Hui

机构信息

State Key Laboratory of Bioactive Molecules and Druggability Assessment, Jinan University, Guangzhou, 510632, China.

Department of Immunology and Microbiology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.

出版信息

Acta Pharmacol Sin. 2025 Feb;46(2):430-447. doi: 10.1038/s41401-024-01376-8. Epub 2024 Sep 2.

Abstract

PANoptosis is an emerging form of regulated cell death (RCD) characterized by simultaneous activation of pyroptotic, apoptotic, and necroptotic signaling that not only participates in pathologies of inflammatory diseases but also has a critical role against pathogenic infections. Targeting PANoptosis represents a promising therapeutic strategy for related inflammatory diseases, but identification of inhibitors for PANoptosis remains an unmet demand. Baicalin () is an active flavonoid isolated from Scutellaria baicalensis Georgi (Huangqin), a traditional Chinese medicinal herb used for heat-clearing and detoxifying. Numerous studies suggest that baicalin possesses inhibitory activities on various forms of RCD including apoptosis/secondary necrosis, pyroptosis, and necroptosis, thereby mitigating inflammatory responses. In this study we investigated the effects of baicalin on PANoptosis in macrophage cellular models. Primary macrophages (BMDMs) or J774A.1 macrophage cells were treated with 5Z-7-oxozeaenol (OXO, an inhibitor for TAK1) in combination with TNF-α or LPS. We showed that OXO plus TNF-α or LPS induced robust lytic cell death, which was dose-dependently inhibited by baicalin (50-200 μM). We demonstrated that PANoptosis induction was accompanied by overt mitochondrial injury, mitochondrial DNA (mtDNA) release and Z-DNA formation. Z-DNA was formed from cytosolic oxidized mtDNA. Both oxidized mtDNA and mitochondrial Z-DNA puncta were co-localized with the PANoptosome (including ZBP1, RIPK3, ASC, and caspase-8), a platform for mediating PANoptosis. Intriguingly, baicalin not only prevented mitochondrial injury but also blocked mtDNA release, Z-DNA formation and PANoptosome assembly. Knockdown of ZBP1 markedly decreased PANoptotic cell death. In a mouse model of hemophagocytic lymphohistiocytosis (HLH), administration of baicalin (200 mg/kg, i.g., for 4 times) significantly mitigated lung and liver injury and reduced levels of serum TNF-α and IFN-γ, concomitant with decreased levels of PANoptosis hallmarks in these organs. Baicalin also abrogated the hallmarks of PANoptosis in liver-resident macrophages (Kupffer cells) in HLH mice. Collectively, our results demonstrate that baicalin inhibits PANoptosis in macrophages by blocking mitochondrial Z-DNA formation and ZBP1-PANoptosome assembly, thus conferring protection against inflammatory diseases. PANoptosis is a form of regulated cell death displaying simultaneous activation of pyroptotic, apoptotic, and necroptotic signaling. This study shows that induction of PANoptosis is linked to mitochondrial dysfunction and mitochondrial Z-DNA formation. Baicalin inhibits PANoptosis in macrophages in vitro via blocking mitochondrial dysfunction and the mitochondrial Z-DNA formation and thereby impeding the assembly of ZBP1-associated PANoptosome. In a mouse model of hemophagocytic lymphohistiocytosis (HLH), baicalin inhibits the activation of PANoptotic signaling in liver-resident macrophages (Kupffer cells) in vivo, thus mitigating systemic inflammation and multiple organ injury in mice.

摘要

全程序坏死性凋亡是一种新出现的程序性细胞死亡(RCD)形式,其特征是同时激活焦亡、凋亡和坏死性凋亡信号,不仅参与炎症性疾病的病理过程,而且在抵抗病原体感染中起关键作用。靶向全程序坏死性凋亡是治疗相关炎症性疾病的一种有前景的治疗策略,但全程序坏死性凋亡抑制剂的鉴定仍是未满足的需求。黄芩苷是从传统中药黄芩中分离出的一种活性黄酮类化合物,黄芩具有清热燥湿解毒的功效。大量研究表明,黄芩苷对包括凋亡/继发性坏死、焦亡和坏死性凋亡在内的多种程序性细胞死亡形式具有抑制活性,从而减轻炎症反应。在本研究中,我们研究了黄芩苷在巨噬细胞模型中对全程序坏死性凋亡的影响。用5Z-7-氧代玉米烯醇(OXO,TAK1的抑制剂)联合TNF-α或LPS处理原代巨噬细胞(BMDM)或J774A.1巨噬细胞。我们发现,OXO加TNF-α或LPS诱导强烈的溶解性细胞死亡,黄芩苷(50-200μM)可剂量依赖性地抑制这种死亡。我们证明,全程序坏死性凋亡的诱导伴随着明显的线粒体损伤、线粒体DNA(mtDNA)释放和Z-DNA形成。Z-DNA由胞质氧化的mtDNA形成。氧化的mtDNA和线粒体Z-DNA斑点均与全程序坏死小体(包括ZBP1、RIPK3、ASC和caspase-8)共定位,全程序坏死小体是介导全程序坏死性凋亡的平台。有趣的是,黄芩苷不仅能预防线粒体损伤,还能阻止mtDNA释放、Z-DNA形成和全程序坏死小体组装。敲低ZBP1可显著降低全程序坏死性凋亡细胞死亡。在噬血细胞性淋巴组织细胞增生症(HLH)小鼠模型中,给予黄芩苷(200mg/kg,腹腔注射,共4次)可显著减轻肺和肝损伤,降低血清TNF-α和IFN-γ水平,同时降低这些器官中全程序坏死性凋亡标志物的水平。黄芩苷还消除了HLH小鼠肝脏驻留巨噬细胞(库普弗细胞)中全程序坏死性凋亡的标志物。总的来说,我们的结果表明,黄芩苷通过阻断线粒体Z-DNA形成和ZBP1-全程序坏死小体组装来抑制巨噬细胞中的全程序坏死性凋亡,从而对炎症性疾病起到保护作用。全程序坏死性凋亡是一种程序性细胞死亡形式,表现为焦亡、凋亡和坏死性凋亡信号的同时激活。本研究表明,全程序坏死性凋亡的诱导与线粒体功能障碍和线粒体Z-DNA形成有关。黄芩苷通过阻断线粒体功能障碍和线粒体Z-DNA形成,从而阻碍ZBP1相关全程序坏死小体的组装,在体外抑制巨噬细胞中的全程序坏死性凋亡。在噬血细胞性淋巴组织细胞增生症(HLH)小鼠模型中,黄芩苷在体内抑制肝脏驻留巨噬细胞(库普弗细胞)中全程序坏死性凋亡信号的激活,从而减轻小鼠的全身炎症和多器官损伤。

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