University Clinic and Outpatient Clinic for Anesthesiology and Operative Intensive Care, University Medicine Halle (Saale), 06112 Halle (Saale), Germany.
Molecules. 2020 Sep 29;25(19):4466. doi: 10.3390/molecules25194466.
Cellular processes fundamentally depend on protein expression control. At this, protein expression is regulated on the transcriptional and the post-transcriptional level. PUFAs are already known to affect gene transcription. The present study was conducted to answer the question whether PUFAs are also able to impact on the miRNA-mediated post-transcriptional fine-tuning of mRNA copy numbers. To this end, cellular miRNA profiles were screened by means of next-generation sequencing and NanoString analysis to compare PUFA-enriched to unsupplemented endothelial cells exposed to an inflammatory milieu. Validation took place by droplet digital PCR, allowing for an absolute quantification of RNA copy numbers. The analyses revealed that the stimulation-induced upregulation of miR-29a-3p is blocked by PUFA enrichment of endothelial cells. What is more, mRNA copy numbers of miR-29a-3p targets, namely the coagulation factors PAI-1, TF, and vWF, as well as the proinflammatory cytokines IL-1β, IL-6, and IL-8, were reduced in PUFA-enriched endothelial cells compared to unsupplemented cells, counteracting the stimulatory effect of an inflammatory environment. These data hint toward a new mechanism of action by which PUFAs modulate the functionality of endothelial cells. Apparently, the inflammation-modulating properties of PUFAs are also mediated at the post-transcriptional level.
细胞过程从根本上依赖于蛋白质表达控制。在这一点上,蛋白质表达受到转录和转录后水平的调节。多不饱和脂肪酸(PUFAs)已被证明可以影响基因转录。本研究旨在回答多不饱和脂肪酸是否也能够影响 miRNA 介导的 mRNA 拷贝数的转录后微调。为此,通过下一代测序和 NanoString 分析筛选细胞 miRNA 谱,以比较富含 PUFA 的内皮细胞与暴露于炎症环境中的未补充内皮细胞。通过液滴数字 PCR 进行验证,允许对 RNA 拷贝数进行绝对定量。分析表明,PUFA 富集内皮细胞可阻断刺激诱导的 miR-29a-3p 的上调。更重要的是,与未补充细胞相比,富含 PUFA 的内皮细胞中 miR-29a-3p 靶标,即凝血因子 PAI-1、TF 和 vWF 以及促炎细胞因子 IL-1β、IL-6 和 IL-8 的 mRNA 拷贝数减少,抵消了炎症环境的刺激作用。这些数据暗示了 PUFAs 调节内皮细胞功能的新作用机制。显然,PUFAs 的炎症调节特性也在转录后水平介导。