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Spermine and spermidine modulate T-cell function in older adults with and without cognitive decline ex vivo

机译:精霉素和亚精亚胺调节旧成年人的T细胞功能没有认知下降exvivo

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摘要

The global increase in neurodegenerative disorders is one of the most crucial public health issues. Oral polyamine intake was shown to improve memory performance which is thought to be mediated at least in part via increased autophagy induced in brain cells. In Alzheimer’s Disease, T-cells were identified as important mediators of disease pathology. Since autophagy is a central regulator of cell activation and cytokine production, we investigated the influence of polyamines on T-cell activation, autophagy, and the release of Th1/Th2 cytokines from blood samples of patients (n=22) with cognitive impairment or dementia in comparison to healthy controls (n=12) . We found that spermine downregulated all investigated cytokines in a dose-dependent manner. Spermidine led to an upregulation of some cytokines for lower dosages, while high dosages downregulated all cytokines apart from upregulated IL-17A. Autophagy and T-cell activation increased in a dose-dependent manner by incubation with either polyamine. Although effects in patients were seen in lower concentrations, alterations were similar to controls.
机译:神经变性障碍的全球增加是最重要的公共卫生问题之一。显示口腔聚酰胺摄入量提高了内存性能,该记忆性能至少部分地通过脑细胞中诱导的增加的自噬介导。在阿尔茨海默病的疾病中,将T细胞鉴定为疾病病理学的重要介质。由于自噬是细胞活化和细胞因子产生的中央调节因子,我们研究了多胺对T细胞活化,自噬和来自患者血液样本(n = 22)的Th1 / Th2细胞因子的影响,具有认知障碍或痴呆与健康对照相比(n = 12)。我们发现精美以剂量依赖性方式下调所有研究的细胞因子。 Femerminine导致一些细胞因子的上调,用于低剂量,而高剂量分开从上调的IL-17a之外的所有细胞因子下调。通过与多胺孵育,自噬和T细胞活化以剂量依赖性方式增加。虽然患者的效果在较低浓度下,但是改变与对照相似。

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