Nascimento C R, Valente R C, Echevarria-Lima J, Fontes C F L, de Araujo-Martins L, Araujo E G, Rumjanek V M
Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, 21 941-902 Rio de Janeiro, RJ, Brazil ; Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, 21 941-902 Rio de Janeiro, RJ, Brazil.
Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, 21 941-902 Rio de Janeiro, RJ, Brazil.
Mediators Inflamm. 2014;2014:494956. doi: 10.1155/2014/494956. Epub 2014 Dec 28.
Although known as a Na,K-ATPase inhibitor, several other cellular and systemic actions have been ascribed to the steroid Ouabain (Oua). Particularly in the immune system, our group showed that Ouabain acts on decreasing lymphocyte proliferation, synergizing with glucocorticoids in spontaneous thymocyte apoptosis, and also lessening CD14 expression and blocking CD16 upregulation on human monocytes. However, Ouabain effects on dendritic cells (DCs) were not explored so far. Considering the peculiar plasticity and the importance of DCs in immune responses, the aim of our study was to investigate DC maturation under Ouabain influence. To generate immature DCs, human monocytes were cultured with IL-4 and GM-CSF (5 days). To investigate Ouabain role on DC activation, DCs were stimulated with TNF-α for 48 h in the presence or absence of Ouabain. TNF-induced CD83 expression and IL-12 production were abolished in DCs incubated with 100 nM Ouabain, though DC functional capacity concerning lymphocyte activation remained unaltered. Nevertheless, TNF-α-induced antigen capture downregulation, another maturation marker, occurred even in the presence of Ouabain. Besides, Ouabain increased HLA-DR and CD86 expression, whereas CD80 expression was maintained. Collectively, our results suggest that DCs respond to Ouabain maturating into a distinct category, possibly contributing to the balance between immunity and tolerance.
尽管已知类固醇哇巴因(Oua)是一种钠钾ATP酶抑制剂,但它还具有其他一些细胞和全身作用。特别是在免疫系统中,我们的研究小组发现,哇巴因可降低淋巴细胞增殖,在自发性胸腺细胞凋亡中与糖皮质激素协同作用,还可降低人单核细胞上CD14的表达并阻止CD16上调。然而,到目前为止,尚未研究哇巴因对树突状细胞(DC)的影响。考虑到DC独特的可塑性及其在免疫反应中的重要性,我们研究的目的是调查哇巴因影响下DC的成熟情况。为了生成未成熟的DC,将人单核细胞与IL-4和GM-CSF一起培养(5天)。为了研究哇巴因对DC激活的作用,在有或没有哇巴因的情况下,用TNF-α刺激DC 48小时。在与100 nM哇巴因孵育的DC中,TNF诱导的CD83表达和IL-12产生被消除,尽管DC在淋巴细胞激活方面的功能能力保持不变。然而,即使在有哇巴因的情况下,另一个成熟标志物TNF-α诱导的抗原捕获下调也会发生。此外,哇巴因增加了HLA-DR和CD86的表达,而CD80的表达保持不变。总体而言,我们的结果表明,DC对哇巴因有反应,成熟为一个独特的类别,可能有助于免疫和耐受之间的平衡。