Hypertonic induction of COX2 expression requires TonEBP/NFAT5 in renal epithelial cells

被引:34
|
作者
Favale, N. O. [1 ]
Casali, C. I. [1 ]
Lepera, L. G. [1 ]
Pescio, L. G. [1 ]
Fernandez-Tome, M. C. [1 ]
机构
[1] Univ Buenos Aires, Sch Pharm & Biochem, Dept Biol Sci, IQUIFIB CONICET, Buenos Aires, DF, Argentina
关键词
COX2; regulation; TonEBP/NFAT5; Osmoprotection; Hypertonic stress; MEDULLARY INTERSTITIAL-CELLS; ACTIVATED T-CELLS; CYCLOOXYGENASE-2; EXPRESSION; TRANSCRIPTIONAL ACTIVATOR; GENE-TRANSCRIPTION; CELLULAR-RESPONSE; OSMOTIC-STRESS; NUCLEAR FACTOR; MDCK CELLS; SURVIVAL;
D O I
10.1016/j.bbrc.2008.12.189
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2009 Published by Elsevier Inc.
引用
收藏
页码:301 / 305
页数:5
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