Key result
Depletion of sorting nexin 1 (SNX1) impaired dopamine D5 receptor endocytosis and signaling in vitro, and increased blood pressure while blunting natriuretic responses in mice.
SNX1 is crucial for D5R trafficking and function, and its depletion leads to D5R dysfunction and hypertension, suggesting a novel mechanism for the pathogenesis of essential hypertension.
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 (D(5)R) 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 D(5)R and in mice. Silencing of SNX1 expression via RNAi resulted in the failure of D(5)R 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 D(5)R. 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 D(5)R trafficking and that SNX1 depletion results in D(5)R dysfunction and thus may represent a novel mechanism for the pathogenesis of essential hypertension.
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Villar et al. (2012) studied Hypertension. SNX1 depletion vs. Mock siRNA or vehicle was evaluated on Blood pressure and D5R signaling. Depletion of sorting nexin 1 (SNX1) impaired dopamine D5 receptor endocytosis and signaling in vitro, and increased blood pressure while blunting natriuretic responses in mice.
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