Department of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon, South Korea.
Cell Mol Neurobiol. 2013 Mar;33(2):223-32. doi: 10.1007/s10571-012-9889-0. Epub 2012 Nov 20.
The maintenance of water homeostasis under pathological conditions is mediated by the aquaporin-4 (AQP4) channel in astrocytes. To clarify the transcriptional regulation for AQP4 under conditions of astrocytic swelling, we examined the role of nuclear factor of activated T cells 5 (NFAT5). We evaluated NFAT5 expression patterns after the induction of brain edema and following excitotoxic neuronal death by kainic acid injection. In injured hippocampi, NFAT5 expression increased in astrocytes from 12 h to 3 days post-injection. AQP4 was redistributed from perivascular to whole-cell processes in astrocytes. NFAT5 and AQP4 expression increased under astrocytic swelling induced by ammonia treatment, and NFAT5-targeted silencing significantly reduced AQP4 expression. The promoter region required for NFAT5 transcriptional activation was located between -49 and -38 bp of rat AQP4. The amount of NFAT5 bound to the promoter of AQP4 was increased in response to ammonia. Our data demonstrate that NFAT5 is necessary for the transcriptional regulation of AQP4 expression and for local astrocyte swelling with accompanying restriction of the neuropil extracellular space in vivo.
水稳态在病理条件下的维持是由星形胶质细胞中的水通道蛋白-4 (AQP4) 通道介导的。为了阐明星形胶质细胞肿胀条件下 AQP4 的转录调控,我们研究了活化 T 细胞核因子 5 (NFAT5) 的作用。我们评估了脑水肿诱导后和海人酸注射引起兴奋性神经元死亡后 NFAT5 的表达模式。在损伤的海马中,NFAT5 表达在注射后 12 小时至 3 天在星形胶质细胞中增加。AQP4 在星形胶质细胞中从血管周围到全细胞过程重新分布。氨处理诱导星形胶质细胞肿胀时,NFAT5 和 AQP4 的表达增加,NFAT5 靶向沉默显著降低 AQP4 的表达。NFAT5 转录激活所需的启动子区域位于大鼠 AQP4 的-49 至-38 bp 之间。氨响应时,与 AQP4 启动子结合的 NFAT5 量增加。我们的数据表明,NFAT5 对于 AQP4 表达的转录调控以及体内伴随神经突细胞外空间限制的局部星形胶质细胞肿胀是必需的。