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Cutaneous Na+ Storage Strengthens the Antimicrobial Barrier Function of the Skin and Boosts Macrophage-Driven Host Defense

机译:钠离子的皮肤储存增强了皮肤的抗菌屏障功能,并增强了巨噬细胞驱动的宿主防御

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Immune cells regulate a hypertonic microenvironment in the skin; however, the biological advantage of increased skin Na+ concentrations is unknown. We found that Na+ accumulated at the site of bacterial skin infections in humans and in mice. We used the protozoan parasite Leishmania major as a model of skin-prone macrophage infection to test the hypothesis that skin-Na+ storage facilitates antimicrobial host defense. Activation of macrophages in the presence of high NaCl concentrations modified epigenetic markers and enhanced p38 mitogen-activated protein kinase (p38/MAPK)dependent nuclear factor of activated T cells 5 (NFAT5) activation. This high-salt response resulted in elevated type-2 nitric oxide synthase (Nos2)-dependent NO production and improved Leishmania major control. Finally, we found that increasing Na+ content in the skin by a high-salt diet boosted activation of macrophages in a Nfat5-dependent manner and promoted cutaneous antimicrobial defense. We suggest that the hypertonic microenvironment could serve as a barrier to infection.
机译:免疫细胞调节皮肤中的高渗微环境。然而,增加皮肤Na +浓度的生物学优势尚不明确。我们发现,Na +在人类和小鼠的细菌性皮肤感染部位积累。我们使用原生动物寄生虫利什曼原虫作为易发皮肤巨噬细胞感染的模型,以测试皮肤Na +储存有助于抗菌宿主防御的假设。在高NaCl浓度下巨噬细胞的活化修饰了表观遗传标记并增强了活化T细胞5(NFAT5)活化的p38丝裂原活化蛋白激酶(p38 / MAPK)依赖性核因子。这种高盐反应导致升高的2型一氧化氮合酶(Nos2)依赖性NO产生并改善了利什曼原虫的主要控制。最后,我们发现通过高盐饮食增加皮肤中的Na +含量会以Nfat5依赖的方式促进巨噬细胞的活化,并促进皮肤抗菌素的防御。我们建议高渗微环境可以作为感染的屏障。

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