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Changes of KEAP1/NRF2 and IKB/NF-κB Expression Levels Induced by Cell-Free DNA in Different Cell Types

机译:不同细胞类型的无细胞DNA诱导的KEAP1 / NRF2和IKB /NF-κB表达水平的变化

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摘要

Cell-free DNA (cfDNA) is a circulating DNA of nuclear and mitochondrial origin mainly derived from dying cells. Recent studies have shown that cfDNA is a stress signaling DAMP (damage-associated molecular pattern) molecule. We report here that the expression profiles of cfDNA-induced factors NRF2 and NF-κB are distinct depending on the target cell's type and the GC-content and oxidation rate of the cfDNA. Stem cells (MSC) have shown higher expression of NRF2 without inflammation in response to cfDNA. In contrast, inflammatory response launched by NF-κB was dominant in differentiated cells HUVEC, MCF7, and fibroblasts, with a possibility of transition to massive apoptosis. In each cell type examined, the response for oxidized cfDNA was more acute with higher peak intensity and faster resolution than that for nonoxidized cfDNA. GC-rich nonoxidized cfDNA evoked a weaker and prolonged response with proinflammatory component (NF-κB) as predominant. The exploration of apoptosis rates after adding cfDNA showed that cfDNA with moderately increased GC-content and lightly oxidized DNA promoted cell survival in a hormetic manner. Novel potential therapeutic approaches are proposed, which depend on the current cfDNA content: either preconditioning with low doses of cfDNA before a planned adverse impact or eliminating (binding, etc.) cfDNA when its content has already become high.
机译:无细胞DNA(cfDNA)是主要来自垂死细胞的核和线粒体起源的循环DNA。最近的研究表明,cfDNA是一种应力信号转导的DAMP(损伤相关分子模式)分子。我们在这里报告,cfDNA诱导因子NRF2和NF-κB的表达谱是不同的,具体取决于靶细胞的类型以及cfDNA的GC含量和氧化速率。干细胞(MSC)已显示出对cfDNA响应而无炎症的NRF2较高表达。相比之下,NF-κB引发的炎症反应在分化的细胞HUVEC,MCF7和成纤维细胞中占主导,并可能转变为大量凋亡。在每种检查的细胞类型中,与未氧化的cfDNA相比,氧化的cfDNA的响应更为尖锐,具有更高的峰强度和更快的分辨率。富含GC的非氧化cfDNA引起的炎症反应较弱且持续时间较长,而促炎成分(NF-κB)为主导。加入cfDNA后对细胞凋亡率的探索表明,具有适度增加的GC含量和轻度氧化的DNA的cfDNA以一种有毒的方式促进了细胞的存活。提出了新的潜在治疗方法,该方法取决于当前cfDNA的含量:在计划的不利影响之前用低剂量的cfDNA进行预处理,或者在含量已经很高时消除(结合等)cfDNA。

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