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木樨草素通过阻断 ASC 寡聚化抑制 NLRP3 炎性小体激活。

Luteolin inhibits NLRP3 inflammasome activation via blocking ASC oligomerization.

机构信息

Hard-tissue Biointerface Research Center, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.

Department of Food and Nutrition, Chungbuk National University, Chundae-ro 1, Seowon-gu, Cheongju, Republic of Korea.

出版信息

J Nutr Biochem. 2021 Jun;92:108614. doi: 10.1016/j.jnutbio.2021.108614. Epub 2021 Mar 8.

Abstract

The NLRP3 inflammasome is a caspase-1 containing multi-protein complex that controls the release of IL-1β and plays important roles in the innate immune response. Since NLRP3 inflammasome is implicated in the pathogenesis of a variety of diseases, it has become an increasingly interested target in developing therapies for multiple diseases. We reported the current study to determine how luteolin, a natural phenolic compound found in many vegetables and medicinal herbs, would modulate NLRP3 inflammasome in both the in vivo and in vitro settings. First, we found that a high-fat diet upregulated mRNA expression of NLRP3 inflammasome components Asc and Casp1 in adipose tissue of ovariectomized mice, which were greatly reduced by dietary supplementation with luteolin. Of note, Asc and Casp1 expression in adipose tissue correlated with mRNA levels of Adgre1 encoding F4/80, an established marker for mature macrophages. We also demonstrated that luteolin inhibited NLRP3 inflammasome-derived caspase-1 activation and IL-1β secretion in J774A.1 macrophages upon diverse stimuli including ATP, nigericin, or silica crystals. Luteolin inhibited the activation step of NLRP3 inflammasome by interfering with ASC oligomerization. Taken together, these findings suggest that luteolin supplementation may suppress NLRP3 induction and activation process and thus potentially would be protective against NLRP3-mediated inflammatory diseases.

摘要

NLRP3 炎性小体是一种包含半胱天冬酶-1 的多蛋白复合物,可控制 IL-1β 的释放,并在先天免疫反应中发挥重要作用。由于 NLRP3 炎性小体与多种疾病的发病机制有关,因此它已成为开发多种疾病治疗方法的一个日益受到关注的靶点。我们开展了这项研究,旨在确定木犀草素(一种在许多蔬菜和草药中发现的天然酚类化合物)如何在体内和体外环境中调节 NLRP3 炎性小体。首先,我们发现高脂肪饮食会增加去卵巢小鼠脂肪组织中 NLRP3 炎性小体成分 Asc 和 Casp1 的 mRNA 表达,而用木犀草素饮食补充则大大减少了这些表达。值得注意的是,脂肪组织中 Asc 和 Casp1 的表达与编码 F4/80(成熟巨噬细胞的公认标志物)的 Adgre1 mRNA 水平相关。我们还证明,木犀草素可抑制不同刺激物(包括 ATP、 Nigericin 或二氧化硅晶体)作用下 J774A.1 巨噬细胞中 NLRP3 炎性小体衍生的半胱天冬酶-1 激活和 IL-1β 分泌。木犀草素通过干扰 ASC 寡聚化来抑制 NLRP3 炎性小体的激活步骤。总之,这些发现表明,木犀草素补充可能会抑制 NLRP3 的诱导和激活过程,从而可能对 NLRP3 介导的炎症性疾病具有保护作用。

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