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褪黑素改变了小鼠小神经胶质细胞中炎症小体激活的 miRNA 转录组。

Melatonin Alters the miRNA Transcriptome of Inflammasome Activation in Murine Microglial Cells.

机构信息

Izmir Biomedicine and Genome Center, 35340, Izmir, Balcova, Turkey.

Izmir International Biomedicine and Genome Institute, Dokuz Eylul University, 35340, Izmir, Turkey.

出版信息

Neurochem Res. 2022 Oct;47(10):3202-3211. doi: 10.1007/s11064-022-03674-1. Epub 2022 Jul 16.

Abstract

Systemic inflammation can have devastating effects on the central nervous system via its resident immune cells, the microglia. One of the primary mediators of this inflammation is inflammasomes, multiprotein complexes that trigger a release of inflammatory proteins when activated. Melatonin, a hormone with anti-inflammatory effects, is an attractive candidate for suppressing such inflammation. In this study, we have investigated how melatonin alters the microRNA (miRNA) transcriptome of microglial cells. For that purpose, we have performed RNA sequencing on a lipopolysaccharide and adenosine triphosphate (LPS + ATP) induced NLR family pyrin domain containing 3 (NLRP3) inflammasome activation model in the N9 mouse microglial cell line, with and without melatonin pre-treatment. We have identified 136 differentially expressed miRNAs in cells exposed to LPS + ATP compared to controls and 10 differentially expressed miRNAs in melatonin pre-treated cells compared to the inflammasome group. We have identified miR-155-3p as a miRNA that is upregulated with inflammasome activation and downregulated with melatonin treatment. We further confirmed this pattern of miR-155-3p expression in the brains of mice injected intraperitoneally with LPS. Moreover, an overexpression study with miRNA-155-3p mimic supported the idea that the protective effects of melatonin in NLRP3 inflammasome activation are partly associated with miRNA-155-3p inhibition.

摘要

系统性炎症可以通过其常驻免疫细胞——小胶质细胞对中枢神经系统造成毁灭性影响。这种炎症的主要介质之一是炎性体,这是一种多蛋白复合物,当被激活时会引发炎症蛋白的释放。褪黑素是一种具有抗炎作用的激素,是抑制这种炎症的有吸引力的候选物。在这项研究中,我们研究了褪黑素如何改变小胶质细胞的 microRNA(miRNA)转录组。为此,我们在 N9 小鼠小胶质细胞系中进行了脂多糖和三磷酸腺苷(LPS+ATP)诱导的 NLR 家族包含 pyrin 域 3(NLRP3)炎性体激活模型的 RNA 测序,同时进行了褪黑素预处理。与对照组相比,在 LPS+ATP 暴露的细胞中鉴定出 136 个差异表达的 miRNA,与炎性体组相比,在褪黑素预处理的细胞中鉴定出 10 个差异表达的 miRNA。我们确定 miR-155-3p 是一种随着炎性体激活而上调且随着褪黑素处理而下调的 miRNA。我们进一步在经腹腔注射 LPS 的小鼠大脑中证实了 miR-155-3p 表达的这种模式。此外,miR-155-3p 模拟物的过表达研究支持这样的观点,即褪黑素在 NLRP3 炎性体激活中的保护作用部分与 miR-155-3p 抑制有关。

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