Ferraris Joan D, Burg Maurice B
Laboratory of Kidney and Electrolyte Metabolism, National Heart Lung Blood Institute, National Institutes of Health, DHHS, Bethesda, Md., USA.
Contrib Nephrol. 2006;152:125-141. doi: 10.1159/000096320.
Cells in the renal medulla are normally exposed to levels of NaCl that are extremely high and that vary with concentration of the urine. Such high levels of NaCl cause cellular perturbations, including increased DNA double-strand breaks, increased oxidation of DNA and proteins, and cytoskeletal alterations. Despite these perturbations the cells are able to survive and function because of osmoprotective responses that include accumulation of compatible organic osmolytes and increased abundance of heat shock proteins and water channels. Many of the responses are initiated by increased gene transcription, directed by the transcription factor TonEBP/OREBP. Here, we review the sensors of hypertonicity, the signaling pathways to TonEBP/OREBP, and the ways in which it is activated to increase transcription. Multiple signals are involved, including some that arise directly from the cellular perturbations caused by hypertonicity. Although the combination of these signals is necessary for full osmotic activation of TonEBP/OREBP, no one of them, alone, is sufficient. We conclude that hypertonicity profoundly alters the state of cells, providing numerous interrelated inputs to the osmoregulatory network.
肾髓质中的细胞通常暴露于极高水平的氯化钠中,且该水平会随尿液浓度而变化。如此高浓度的氯化钠会引发细胞紊乱,包括DNA双链断裂增加、DNA和蛋白质氧化加剧以及细胞骨架改变。尽管存在这些紊乱,但细胞仍能存活并发挥功能,这是因为存在渗透保护反应,包括相容性有机渗透溶质的积累以及热休克蛋白和水通道丰度的增加。许多反应是由转录因子TonEBP/OREBP指导的基因转录增加引发的。在此,我们综述了高渗传感器、通向TonEBP/OREBP的信号通路以及其被激活以增加转录的方式。涉及多种信号,包括一些直接源于高渗引起的细胞紊乱的信号。尽管这些信号的组合对于TonEBP/OREBP的完全渗透激活是必要的,但其中任何一个信号单独都不足以激活。我们得出结论,高渗会深刻改变细胞状态,为渗透调节网络提供众多相互关联的输入。