Pham Tho X, Park Young-Ki, Lee Ji-Young
Department of Nutritional Sciences, University of Connecticut, Storrs, CT 06269, USA.
Nutrients. 2016 Jun 21;8(6):381. doi: 10.3390/nu8060381.
We previously demonstrated that the organic extract of Spirulina platensis (SPE), an edible blue-green alga, possesses potent anti-inflammatory effects. In this study, we investigated if the regulation of histone deacetylases (HDACs) play a role in the anti-inflammatory effect of SPE in macrophages. Treatment of macrophages with SPE rapidly and dose-dependently reduced HDAC2, 3, and 4 proteins which preceded decreases in their mRNA levels. Degradation of HDAC4 protein was attenuated in the presence of inhibitors of calpain proteases, lysosomal acidification, and Ca(2+)/calmodulin-dependent protein kinase II, respectively, but not a proteasome inhibitor. Acetylated histone H3 was increased in SPE-treated macrophages to a similar level as macrophages treated with a pan-HDAC inhibitor, with concomitant inhibition of inflammatory gene expression upon LPS stimulation. Knockdown of HDAC3 increased basal and LPS-induced pro-inflammatory gene expression, while HDAC4 knockdown increased basal expression of interleukin-1β (IL-1β), but attenuated LPS-induced inflammatory gene expression. Chromatin immunoprecipitation showed that SPE decreased p65 binding and H3K9/K14 acetylation at the Il-1β and tumor necrosis factor α (Tnfα) promoters. Our results suggest that SPE increased global histone H3 acetylation by facilitating HDAC protein degradation, but decreases histone H3K9/K14 acetylation and p65 binding at the promoters of Il-1β and Tnfα to exert its anti-inflammatory effect.
我们之前证明,可食用蓝绿藻钝顶螺旋藻的有机提取物(SPE)具有强大的抗炎作用。在本研究中,我们调查了组蛋白脱乙酰酶(HDACs)的调节是否在巨噬细胞中SPE的抗炎作用中发挥作用。用SPE处理巨噬细胞可迅速且剂量依赖性地降低HDAC2、3和4蛋白水平,这先于其mRNA水平的下降。HDAC4蛋白的降解分别在钙蛋白酶、溶酶体酸化和Ca(2+)/钙调蛋白依赖性蛋白激酶II的抑制剂存在时减弱,但在蛋白酶体抑制剂存在时未减弱。在经SPE处理的巨噬细胞中,乙酰化组蛋白H3增加至与用泛HDAC抑制剂处理的巨噬细胞相似的水平,同时在LPS刺激下炎症基因表达受到抑制。敲低HDAC3会增加基础和LPS诱导的促炎基因表达,而敲低HDAC4会增加白细胞介素-1β(IL-1β)的基础表达,但会减弱LPS诱导的炎症基因表达。染色质免疫沉淀显示,SPE降低了Il-1β和肿瘤坏死因子α(Tnfα)启动子处的p65结合以及H3K9/K14乙酰化。我们的结果表明,SPE通过促进HDAC蛋白降解增加了整体组蛋白H3乙酰化,但降低了Il-1β和Tnfα启动子处的组蛋白H3K9/K14乙酰化和p65结合,从而发挥其抗炎作用。