Institute of Biophysics of the Czech Academy of Sciences, 612 65, Brno, Czech Republic; International Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Institute of Biophysics of the Czech Academy of Sciences, 612 65, Brno, Czech Republic.
Food Chem Toxicol. 2020 Jul;141:111348. doi: 10.1016/j.fct.2020.111348. Epub 2020 May 4.
Natural pseurotins, secondary metabolites of fungi, commonly produced by various species such as Aspergillus flavus with suggested significant biological effects. However, little is known about effects of pseurotins on immune system functions.
Effects of pseurotin A and D on proliferation and viability of macrophage RAW 264.7 cells were evaluated together with mitochondrial respiration and glycolysis. Macrophage response to lipopolysaccharide was analyzed based on determination of nitric oxide (NO) production, expression of inducible NO synthase (iNOS), interleukin 6 (IL-6) and tumor necrosis factor production. Activation of selected signaling pathways, particularly STAT and MAPK, as well as expression of cyclins were determined.
Natural pseurotins A and D in concentrations of up to 50 μM significantly inhibit proliferation of RAW 264.7 macrophages which was not complemented by induction of cell toxicity. The inhibition of cell proliferation was accompanied by downregulation of expression of cyclins and mitochondrial respiration via inhibition of particularly STAT3 phosphorylation. Both pseurotins significantly inhibited production of NO, expression of iNOS and IL-6 production.
Our results advance the current mechanistic understanding of the pseurotin-induced inhibition of proliferation, metabolic respiration and functional responses in macrophages by linking the effect to JAK/STAT signaling pathway.
天然假壳菌素是真菌的次生代谢产物,通常由黄曲霉等多种物种产生,具有显著的生物学效应。然而,关于假壳菌素对免疫系统功能的影响知之甚少。
评估了假壳菌素 A 和 D 对巨噬细胞 RAW 264.7 细胞增殖和活力的影响,同时评估了线粒体呼吸和糖酵解。根据一氧化氮(NO)产生、诱导型一氧化氮合酶(iNOS)、白细胞介素 6(IL-6)和肿瘤坏死因子产生的表达,分析了巨噬细胞对脂多糖的反应。确定了选定信号通路的激活,特别是 STAT 和 MAPK,以及细胞周期蛋白的表达。
浓度高达 50 μM 的天然假壳菌素 A 和 D 可显著抑制 RAW 264.7 巨噬细胞的增殖,而不会导致细胞毒性。细胞增殖的抑制伴随着细胞周期蛋白和线粒体呼吸的下调,这是通过抑制 STAT3 磷酸化来实现的。这两种假壳菌素都能显著抑制 NO 的产生、iNOS 的表达和 IL-6 的产生。
我们的结果通过将假壳菌素诱导的增殖、代谢呼吸和巨噬细胞功能反应的抑制作用与 JAK/STAT 信号通路联系起来,推进了对假壳菌素诱导的抑制作用的机制理解。