SORLA/SORL1 Functionally Interacts with SPAK To Control Renal Activation of Na⁺-K⁺-Cl⁻ Cotransporter 2

Abstract

Proper control of NaCl excretion in the kidney is central to bodily functions, yet many mechanisms that regulate reabsorption of sodium and chloride in the kidney remain incompletely understood. Here, we identify an important role played by the intracellular sorting receptor SORLA (sorting protein-related receptor with A-type repeats) in functional activation of renal ion transporters. We demonstrate that SORLA is expressed in epithelial cells of the thick ascending limb (TAL) of Henle's loop and that lack of receptor expression in this cell type in SORLA-deficient mice results in an inability to properly reabsorb sodium and chloride during osmotic stress. The underlying cellular defect was correlated with an inability of the TAL to phosphorylate Na⁺-K⁺-Cl⁻ cotransporter 2 (NKCC2), the major sodium transporter in the distal nephron. SORLA functionally interacts with Ste-20-related proline-alanine-rich kinase (SPAK), an activator of NKCC2, and receptor deficiency is associated with missorting of SPAK. Our data suggest a novel regulatory pathway whereby intracellular trafficking of SPAK by the sorting receptor SORLA is crucial for proper NKCC2 activation and for maintenance of renal ion balance.

We are indebted to M. Schmeisser, K. Riskowsky, R. Plehm, H. Sidelmann, and K. Kampf for technical assistance and to I. Giménez (University of Zaragoza) and D. Müller (Charité, Berlin, Germany) for helpful discussions.

These studies were funded in part by the DFG (FG667) and the Lundbeck Foundation.