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[2,6-二甲氧基-1,4-苯醌通过抑制NLRP3炎性小体激活减轻小鼠脓毒症休克]

[2, 6-dimethoxy-1, 4-benzoquinone alleviates septic shock in mice by inhibiting NLRP3 inflammasome activation].

作者信息

Zhang W, Deng M, Zeng Y, Liu C, Shang F, Xu W, Jiang H, Wang F, Yang Y

机构信息

Clinical Laboratory, First Affiliated Hospital of Bengbu Medical University, Bengbu 233004, China.

Anhui Provincial Key Laboratory of Immunology in Chronic Diseases, Bengbu Medical University, Bengbu 233030, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2024 Jun 20;44(6):1024-1032. doi: 10.12122/j.issn.1673-4254.2024.06.02.

Abstract

OBJECTIVE

To investigate the mechanism of 2, 6-dimethoxy-1, 4-benzoquinone (DMQ), an active ingredients in fermented wheat germ extract, for inhibiting NLRP3 inflammasome activation and alleviating septic shock in mice.

METHODS

Cultured murine bone marrow-derived macrophages (BMDM) stimulated with lipopolysaccharide (LPS) were treated with DMQ, followed by treatment with Nigericin, ATP, and MSU for activating the canonical NLRP3 inflammasome; the noncanonical NLRP3 inflammasome was activated by intracellular transfection of LPS, and AIM2 inflammasome was activated using Poly A: T.In human monocytic THP-1 cells, the effect of Nigericin on inflammasome activation products was examined using Western blotting and ELISA.Co-immunoprecipitation was performed to explore the mechanism of DMQ-induced blocking of NLRP3 inflammasome activation.In a male C57BL/6J mouse model of LPS-induced septic shock treated with 20 and 40 mg/kg DMQ, the levels of IL-1β and TNF-α in the serum and peritoneal lavage fluid were determined using ELISA, and the survival time of the mice within 36 h was observed.

RESULTS

Treatment with DMQ effectively inhibited LPS-induced activation of canonical NLRP3 inflammasome in mouse BMDM and human THP-1 cells and also inhibited non-canonical NLRP3 inflammasome activation in mouse BMDM, but produced no significant effect on AIM2 inflammasome activation.DMQ significantly blocked the binding between ASC and NLRP3.In the mouse models of septic shock, DMQ treatment significantly reduced the levels of IL-1β in the serum and peritoneal fluid and obviously prolonged survival time of the mice.

CONCLUSION

DMQ can effectively block ASC-NLRP3 interaction to inhibit NLRP3 inflammasome activation and alleviate LPSinduced septic shock in mice.

摘要

目的

探讨发酵小麦胚芽提取物中的活性成分2,6 - 二甲氧基 - 1,4 - 苯醌(DMQ)抑制NLRP3炎性小体激活及减轻小鼠脓毒症休克的机制。

方法

用脂多糖(LPS)刺激培养的小鼠骨髓来源巨噬细胞(BMDM),然后用DMQ处理,再用尼日利亚菌素、ATP和微晶尿酸钠(MSU)处理以激活经典NLRP3炎性小体;通过细胞内转染LPS激活非经典NLRP3炎性小体,使用聚腺苷酸:胸腺嘧啶核苷酸(Poly A:T)激活AIM2炎性小体。在人单核细胞THP - 1细胞中,用蛋白质免疫印迹法和酶联免疫吸附测定法检测尼日利亚菌素对炎性小体激活产物的影响。进行免疫共沉淀以探究DMQ诱导阻断NLRP3炎性小体激活的机制。在经20和40 mg/kg DMQ处理的LPS诱导的雄性C57BL/6J小鼠脓毒症休克模型中,用酶联免疫吸附测定法测定血清和腹腔灌洗液中白细胞介素 - 1β(IL - 1β)和肿瘤坏死因子 - α(TNF - α)的水平,并观察小鼠36小时内的存活时间。

结果

DMQ处理有效抑制了LPS诱导的小鼠BMDM和人THP - 1细胞中经典NLRP3炎性小体的激活,并且抑制了小鼠BMDM中非经典NLRP3炎性小体的激活,但对AIM2炎性小体激活没有显著影响。DMQ显著阻断了凋亡相关斑点样蛋白(ASC)与NLRP3之间的结合。在脓毒症休克小鼠模型中,DMQ处理显著降低了血清和腹腔液中IL - 1β的水平,并明显延长了小鼠的存活时间。

结论

DMQ可有效阻断ASC - NLRP3相互作用,抑制NLRP3炎性小体激活,并减轻LPS诱导的小鼠脓毒症休克。

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Nan Fang Yi Ke Da Xue Xue Bao. 2022 Dec 20;42(12):1747-1754. doi: 10.12122/j.issn.1673-4254.2022.12.01.

本文引用的文献

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Structural Mechanisms of NLRP3 Inflammasome Assembly and Activation.NLRP3 炎性小体组装和激活的结构机制。
Annu Rev Immunol. 2023 Apr 26;41:301-316. doi: 10.1146/annurev-immunol-081022-021207. Epub 2023 Feb 7.
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How location and cellular signaling combine to activate the NLRP3 inflammasome.位置和细胞信号如何结合激活 NLRP3 炎性体。
Cell Mol Immunol. 2022 Nov;19(11):1201-1214. doi: 10.1038/s41423-022-00922-w. Epub 2022 Sep 20.
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Targeting the NLRP3 inflammasome in cardiovascular diseases.针对心血管疾病中的 NLRP3 炎性小体。
Pharmacol Ther. 2022 Aug;236:108053. doi: 10.1016/j.pharmthera.2021.108053. Epub 2021 Dec 11.

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