Controlled aquaporin-2 expression in the hypertonic environment

被引:20
作者
Hasler, Udo [1 ]
机构
[1] Fdn Rech Med, Serv Nephrol, CH-1211 Geneva 4, Switzerland
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2009年 / 296卷 / 04期
基金
瑞士国家科学基金会;
关键词
osmolality; vasopressin; collecting ducts; nuclear factor-kappa B; mitogen-activated protein; kinase; TonEBP; RENAL COLLECTING DUCT; WATER CHANNEL EXPRESSION; ENHANCER-BINDING PROTEIN; CELL-VOLUME REGULATION; THICK ASCENDING LIMB; FACTOR-KAPPA-B; NA-K-ATPASE; TRANSPORTER SURFACE EXPRESSION; NEPHROGENIC DIABETES-INSIPIDUS; VASOPRESSIN TYPE-2 RECEPTOR;
D O I
10.1152/ajpcell.00655.2008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hasler U. Controlled aquaporin-2 expression in the hypertonic environment. Am J Physiol Cell Physiol 296: C641-C653, 2009. First published February 11, 2009; doi:10.1152/ajpcell.00655.2008.-The corticomedullary osmolality gradient is the driving force for water reabsorption occurring in the kidney. In the collecting duct, this gradient allows luminal water to move across aquaporin (AQP) water channels, thereby increasing urine concentration. However, this same gradient exposes renal cells to great osmotic challenges. These cells must constantly adapt to fluctuations of environmental osmolality that challenge cell volume and incite functional change. This implies profound alterations of cell phenotype regarding water permeability. AQP2 is an essential component of the urine concentration mechanism whose controlled expression dictates apical water permeability of collecting duct principal cells. This review focuses on changes of AQP2 abundance and trafficking in hypertonicity-challenged cells. Intracellular mechanisms governing these events are discussed and the biological relevance of altered AQP2 expression by hypertonicity is outlined.
引用
收藏
页码:C641 / C653
页数:13
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