Abstract

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.

Highlights

  • sorting nexin 1 (SNX1) is a protein involved in the trafficking of internalized receptors

  • D5 receptor (D5R) interacts with SNX1—We initially confirmed the physical interaction between the D5R and SNX1 [18] through coimmunoprecipitation using cell lysates of immortalized human renal proximal tubule cells (hPTCs)

  • We evaluated the dynamics of the D5R-SNX1 interaction via Förster Resonance Energy Transfer (FRET) microscopy of HEK293 cells expressing V5-tagged D5R (HEK293-hD5R)

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Summary

Background

SNX1 is a protein involved in the trafficking of internalized receptors. Results: Inhibition of SNX1 expression leads to failure of D5R endocytosis and signaling. 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 may represent a novel mechanism for the pathogenesis of essential hypertension. Our results show that in human renal proximal tubule cells (hPTCs) and human embryonic kidney (HEK293) cells heterologously expressing human D5R (HEK293-hD5R), the interaction of both proteins is essential for the trafficking and function of the receptor. Alterations in this interaction result in D5R dysfunction and high blood pressure in mice and may be one of the underlying mechanisms in essential hypertension

EXPERIMENTAL PROCEDURES
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