Sorting Nexin 1 Loss Results in D5 Dopamine Receptor Dysfunction in Human Renal Proximal Tubule Cells and Hypertension in Mice

被引:28
作者
Villar, Van Anthony M. [1 ]
Jones, John Edward [1 ]
Armando, Ines [1 ]
Asico, Laureano D. [1 ]
Escano, Crisanto S., Jr. [1 ]
Lee, Hewang [1 ]
Wang, Xiaoyan [1 ]
Yang, Yu [1 ]
Pascua-Crusan, Annabelle M. [1 ]
Palmes-Saloma, Cynthia P. [2 ]
Felder, Robin A. [3 ]
Jose, Pedro A. [1 ]
机构
[1] Childrens Natl Med Ctr, Childrens Res Inst, Ctr Mol Physiol Res, Washington, DC 20010 USA
[2] Univ Philippines, Natl Inst Mol Biol & Biotechnol, Quezon City 1101, Philippines
[3] Univ Virginia, Sch Med, Dept Pathol, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
TRAFFICKING PROPERTIES; TYPE-1; RECEPTOR; BLOOD-PRESSURE; NADPH OXIDASE; KNOCKOUT MICE; II TYPE-1; DEGRADATION; MEMBRANE; KIDNEY; RATS;
D O I
10.1074/jbc.M112.428458
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peripheral dopaminergic system plays a crucial role in blood pressure regulation through its actions on renal hemodynamics and epithelial ion transport. The dopamine D5 receptor (D5R) interacts with sorting nexin 1 (SNX1), a protein involved in receptor retrieval from the trans-Golgi network. In this report, we elucidated the spatial, temporal, and functional significance of this interaction in human renal proximal tubule cells and HEK293 cells stably expressing human D5R and in mice. Silencing of SNX1 expression via RNAi resulted in the failure of D5R to internalize and bind GTP, blunting of the agonist-induced increase in cAMP production and decrease in sodium transport, and up-regulation of angiotensin II receptor expression, of which expression was previously shown to be negatively regulated by D5R. Moreover, siRNA-mediated depletion of renal SNX1 in C57BL/6J and BALB/cJ mice resulted in increased blood pressure and blunted natriuretic response to agonist in salt-loaded BALB/cJ mice. These data demonstrate a crucial role for SNX1 in D5R trafficking and that SNX1 depletion results in D5R dysfunction and thus may represent a novel mechanism for the pathogenesis of essential hypertension.
引用
收藏
页码:152 / 163
页数:12
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