Department of Medicine, Medical University of South Carolina, Charleston, SC 29403, USA.
Am J Physiol Renal Physiol. 2011 Jul;301(1):F44-54. doi: 10.1152/ajprenal.00666.2010. Epub 2011 Mar 23.
N-methyl-D-aspartate receptors (NMDARs) are Ca(2+)-permeable, ligand-gated, nonselective cation channels that function as neuronal synaptic receptors but which are also expressed in multiple peripheral tissues. Here, we show for the first time that NMDAR subunits NR3a and NR3b are highly expressed in the neonatal kidney and that there is continued expression of NR3a in the renal medulla and papilla of the adult mouse. NR3a was also expressed in mIMCD-3 cells, where it was found that hypoxia and hypertonicity upregulated NR3a expression. Using short-hairpin (sh) RNA-based knockdown, a stable inner medullary collecting duct (IMCD) cell line was established that had ∼80% decrease in NR3a. Knockdown cells exhibited an increased basal intracellular calcium concentration, reduced cell proliferation, and increased cell death. In addition, NR3a knockdown cells exhibited reduced water transport in response to the addition of vasopressin, suggesting an alteration in aquaporin-2 (AQP2) expression/function. Consistent with this notion, we demonstrate decreased surface expression of glycosylated AQP2 in IMCD cells transfected with NR3a shRNA. To determine whether this also occurred in vivo, we compared AQP2 levels in wild-type vs. in NR3a(-/-) mice. Total AQP2 protein levels in the outer and inner medulla were significantly reduced in knockout mice compared with control mice. Finally, NR3a(-/-) mice showed a significant delay in their ability to increase urine osmolality during water restriction. Thus NR3a may play a renoprotective role in collecting duct cells. Therefore, under conditions that are associated with high vasopressin levels, NR3a, by maintaining low intracellular calcium levels, protects the function of the principal cells to reabsorb water and thereby increase medullary osmolality.
N-甲基-D-天冬氨酸受体(NMDAR)是 Ca(2+)可渗透、配体门控、非选择性阳离子通道,作为神经元突触受体发挥作用,但也在多种外周组织中表达。在这里,我们首次表明,NR3a 和 NR3b 亚基在新生肾脏中高度表达,并且在成年小鼠的肾脏髓质和乳头中仍有表达。NR3a 也在 mIMCD-3 细胞中表达,在该细胞中发现缺氧和高渗会上调 NR3a 的表达。使用短发夹(sh)RNA 敲低技术,建立了一种稳定的内髓集合管(IMCD)细胞系,该细胞系中 NR3a 的表达降低了约 80%。敲低细胞表现出基础细胞内钙浓度增加、细胞增殖减少和细胞死亡增加。此外,NR3a 敲低细胞对添加血管加压素的水转运减少,表明水通道蛋白-2(AQP2)的表达/功能发生改变。与这一观点一致,我们证明了在转染 NR3a shRNA 的 IMCD 细胞中,糖基化 AQP2 的表面表达减少。为了确定这是否也发生在体内,我们比较了野生型与 NR3a(-/-) 小鼠的 AQP2 水平。与对照组相比,敲除小鼠的外髓和内髓总 AQP2 蛋白水平明显降低。最后,NR3a(-/-) 小鼠在限制水摄入期间增加尿液渗透压的能力显著延迟。因此,NR3a 可能在集合管细胞中发挥肾保护作用。因此,在与血管加压素水平升高相关的条件下,NR3a 通过维持低细胞内钙水平,保护主细胞的功能以重吸收水,从而增加髓质渗透压。