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芦荟下调脂多糖诱导的人巨噬细胞中炎症细胞因子的产生和 NLRP3 炎性体的表达。

Aloe vera downregulates LPS-induced inflammatory cytokine production and expression of NLRP3 inflammasome in human macrophages.

机构信息

Department of Physiology, Medical and Health Science Center, Faculty of Medicine, University of Debrecen, Nagyerdei Blv. 98, Debrecen H-4012, Hungary.

出版信息

Mol Immunol. 2013 Dec;56(4):471-9. doi: 10.1016/j.molimm.2013.05.005. Epub 2013 Aug 1.


DOI:10.1016/j.molimm.2013.05.005
PMID:23911403
Abstract

Aloe vera has been used in traditional herbal medicine as an immunomodulatory agent inducing anti-inflammatory effects. However, its role on the IL-1β inflammatory cytokine production has not been studied. IL-1β production is strictly regulated both at transcriptional and posttranslational levels through the activity of Nlrp3 inflammasome. In this study we aimed to determine the effect of Aloe vera on the molecular mechanisms of Nlrp3 inflammasome-mediated IL-1β production in LPS-activated human THP-1 cells and monocyte-derived macrophages. Our results show that Aloe vera significantly reduced IL-8, TNFα, IL-6 and IL-1β cytokine production in a dose dependent manner. The inhibitory effect was substantially more pronounced in the primary cells. We found that Aloe vera inhibited the expression of pro-IL-1β, Nlrp3, caspase-1 as well as that of the P2X7 receptor in the LPS-induced primary macrophages. Furthermore, LPS-induced activation of signaling pathways like NF-κB, p38, JNK and ERK were inhibited by Aloe vera in these cells. Altogether, we show for the first time that Aloe vera-mediated strong reduction of IL-1β appears to be the consequence of the reduced expression of both pro-IL-1β as well as Nlrp3 inflammasome components via suppressing specific signal transduction pathways. Furthermore, we show that the expression of the ATP sensor P2X7 receptor is also downregulated by Aloe vera that could also contribute to the attenuated IL-1β cytokine secretion. These results may provide a new therapeutic approach to regulate inflammasome-mediated responses.

摘要

库拉索芦荟在传统草药医学中被用作免疫调节剂,具有抗炎作用。然而,其对白细胞介素-1β(IL-1β)炎症细胞因子产生的影响尚未得到研究。IL-1β的产生在转录和翻译后水平受到严格调控,其通过 Nlrp3 炎性小体的活性来实现。在本研究中,我们旨在确定库拉索芦荟对 LPS 激活的人 THP-1 细胞和单核细胞衍生的巨噬细胞中 Nlrp3 炎性小体介导的 IL-1β产生的分子机制的影响。我们的结果表明,库拉索芦荟以剂量依赖的方式显著降低了细胞因子 IL-8、TNFα、IL-6 和 IL-1β 的产生。这种抑制作用在原代细胞中更为明显。我们发现库拉索芦荟抑制了 LPS 诱导的原代巨噬细胞中 pro-IL-1β、Nlrp3、caspase-1 以及 P2X7 受体的表达。此外,库拉索芦荟还抑制了 LPS 诱导的 NF-κB、p38、JNK 和 ERK 等信号通路的激活。总之,我们首次表明,库拉索芦荟介导的 IL-1β 的强烈减少似乎是由于通过抑制特定信号转导通路来降低 pro-IL-1β 和 Nlrp3 炎性小体成分的表达所致。此外,我们还表明,库拉索芦荟还下调了 ATP 传感器 P2X7 受体的表达,这也可能有助于减轻 IL-1β 细胞因子的分泌。这些结果可能为调节炎性小体介导的反应提供新的治疗方法。

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