钙调神经磷酸酶-NFATc信号通路响应钙信号和渗透压应激调节水通道蛋白2(AQP2)的表达。
Calcineurin-NFATc signaling pathway regulates AQP2 expression in response to calcium signals and osmotic stress.
作者信息
Li Song-Zhe, McDill Bradley W, Kovach Paul A, Ding Li, Go William Y, Ho Steffan N, Chen Feng
机构信息
Department of Internal Medicine/Renal Division, Campus Box 8126, Washington University School of Medicine, St. Louis, MO 63110, USA.
出版信息
Am J Physiol Cell Physiol. 2007 May;292(5):C1606-16. doi: 10.1152/ajpcell.00588.2005. Epub 2006 Dec 13.
The aquaporin (AQP)2 channel mediates the reabsorption of water in renal collecting ducts in response to arginine vasopressin (AVP) and hypertonicity. Here we show that AQP2 expression is induced not only by the tonicity-responsive enhancer binding protein (TonEBP)/nuclear factor of activated T cells (NFAT)5-mediated hypertonic stress response but also by the calcium-dependent calcineurin-NFATc pathway. The induction of AQP2 expression by the calcineurin-NFATc pathway can occur in the absence of TonEBP/NFAT5. Mutational and chromatin immunoprecipitation analyses revealed the existence of functional NFAT binding sites within the proximal AQP2 promoter responsible for regulation of AQP2 by NFATc proteins and TonEBP/NFAT5. Contrary to the notion that TonEBP/NFAT5 is the only Rel/NFAT family member regulated by tonicity, we found that hypertonicity promotes the nuclear translocation of NFATc proteins for the subsequent induction of AQP2 expression. Calcineurin activity was also found to be involved in the induction of TonEBP/NFAT5 expression by hypertonicity, thus further defining the signaling mechanisms that underlie the TonEBP/NFAT5 osmotic stress response pathway. The coordinate regulation of AQP2 expression by both osmotic stress and calcium signaling appears to provide a means to integrate diverse extracellular signals into optimal cellular responses.
水通道蛋白(AQP)2通道介导肾集合管中水的重吸收,以响应精氨酸加压素(AVP)和高渗状态。在此我们表明,AQP2的表达不仅由张力反应增强子结合蛋白(TonEBP)/活化T细胞核因子(NFAT)5介导的高渗应激反应所诱导,还由钙依赖性钙调神经磷酸酶-NFATc途径诱导。钙调神经磷酸酶-NFATc途径对AQP2表达的诱导可在不存在TonEBP/NFAT5的情况下发生。突变分析和染色质免疫沉淀分析揭示了AQP2近端启动子内存在功能性NFAT结合位点,其负责NFATc蛋白和TonEBP/NFAT5对AQP2的调控。与认为TonEBP/NFAT5是唯一受张力调节的Rel/NFAT家族成员这一观点相反,我们发现高渗状态促进NFATc蛋白的核转位,进而诱导AQP2表达。还发现钙调神经磷酸酶活性参与高渗状态对TonEBP/NFAT5表达的诱导,从而进一步明确了TonEBP/NFAT5渗透应激反应途径的信号传导机制。渗透应激和钙信号对AQP2表达的协同调节似乎提供了一种将多种细胞外信号整合为最佳细胞反应的方式。