Favale N O, Casali C I, Lepera L G, Pescio L G, Fernández-Tome M C
Department of Biological Sciences, School of Pharmacy and Biochemistry, University of Buenos Aires, IQUIFIB-CONICET, Ciudad Autónoma de Buenos Aires, Junín 956, 1er piso, (C1113AAD), Argentina.
Biochem Biophys Res Commun. 2009 Apr 10;381(3):301-5. doi: 10.1016/j.bbrc.2008.12.189. Epub 2009 Jan 13.
TonEBP/NFAT5 transcription factor is a master regulator of genes involved in osmoprotection. Cyclooxygenase 2 (COX2) has been reported to be a cytoprotective molecule in the inner renal medulla, where cells are physiologically exposed to the highest osmolality of the body. Our aim was to study whether COX2 expression requires TonEBP/NFAT5. Incubation of MDCK cells in hypertonic NaCl medium (500 mOsm/kg H2O) caused fully translocation of TonEBP/NFAT5 from cytoplasm to nucleoplasm and significantly increased COX2 mRNA, protein and activity levels. TonEBP/NFAT5-siRNA prevented hypertonic induction of COX2 mRNA and protein, leading to a depressed-prostaglandin synthesis and to a decreased cell survival. By using COX2-siRNA and COX2 specific inhibitor NS398, we found that cell survival does not depend on endogenous COX2-induced prostaglandin synthesis, but that cytoprotection strongly correlates with COX2 protein levels. These results demonstrate a new function for TonEBP/NFAT5, i.e., to mediate hypertonic-induced COX2 expression, and suggest that osmoprotection strongly depends on COX2 protein levels.
张力增强结合蛋白/活化T细胞核因子5(TonEBP/NFAT5)转录因子是参与渗透保护的基因的主要调节因子。据报道,环氧化酶2(COX2)是肾内髓质中的一种细胞保护分子,该部位的细胞在生理上暴露于体内最高的渗透压环境中。我们的目的是研究COX2的表达是否需要TonEBP/NFAT5。将MDCK细胞置于高渗NaCl培养基(500 mOsm/kg H2O)中孵育,导致TonEBP/NFAT5从细胞质完全转位至核质,并显著增加COX2的mRNA、蛋白质和活性水平。TonEBP/NFAT5小干扰RNA(siRNA)可阻止高渗诱导的COX2 mRNA和蛋白质表达,导致前列腺素合成减少和细胞存活率降低。通过使用COX2-siRNA和COX2特异性抑制剂NS398,我们发现细胞存活并不依赖于内源性COX2诱导的前列腺素合成,但细胞保护作用与COX2蛋白水平密切相关。这些结果证明了TonEBP/NFAT5的一项新功能,即介导高渗诱导的COX2表达,并表明渗透保护作用强烈依赖于COX2蛋白水平。