The distal convoluted tubule (DCT) of the kidney expresses the thiazide-sensitive Na-Cl cotransporter, NCC, a mechanism essential to Na+ reabsorption, control of blood pressure, and K+ secretion. NCC is activated by phosphorylation, which is mediated by a pair of protein kinases: SPAK, a Ste20p-like kinase which directly binds and phosphorylates the cotransporter, and WNK4, an upstream kinase, which phosphorylates and activates SPAK. Increasing consensus is developing that the function of the DCT is to sense and regulate plasma K+ through the modulation of K+ secretion in the aldosterone-sensitive distal nephron (ASDN). The precise mechanism(s) by which the DCT fulfills this function is still not well-understood. Preliminary data collected in the previous funding cycle indicated that even in the presence of a constitutively-active SPAK kinase, increase in plasma K+ still decreases phosphorylation of NCC leading to a first hypothesis that the K+ activated phosphatase, calcineurin, mediates inhibition of the cotransporter (Aim 1). Based on preliminary work that highlights the role of Cab39 adaptor proteins (Cab39 and Cab39l) in facilitating SPAK and WNK function we hypothesize that these proteins play a critical role in the pathway regulating NCC phosphorylation.
In Aim 2, the molecular interaction between Cab39 and SPAK/WNK, the relationship with the Cl- sensitivity of WNK4, and the relevance of the adaptor proteins at the animal level will all be addressed. To account for the relationship between Na+ reabsorption in DCT and K+ secretion in the ASDN, we hypothesize that on top of the well-accepted view that Na+ delivery inversely modulates epithelial Na+ channel and ROMK, there is paracrine communication between the two nephron segments. This novel idea will be addressed in Aim 3. Finally, longer term coupling between the DCT and the ASDN involves significant remodeling for which we now have a precise signaling pathway to study. Through lineage mapping studies and Jagged-1 knockout studies we will test the hypothesis that NOTCH signaling increases the number of principal cells in the connecting segment (Aim 4). These new studies will provide a greater integrated view of the role of Na+ transport in the DCT in renal function.

Public Health Relevance

The WNK/SPAK pathway plays a critical role in the function of the distal convoluted tubule of the kidney by sensing plasma K+ and regulating Na+ reabsorption and K+ secretion through the Na-Cl cotransporter, NCC. Our studies will examine how plasma K+ affects dephosphorylation of the cotransporter; how the adaptor protein Cab39 couples WNK activation to SPAK phosphorylation and activation of NCC; how the DCT communicates through paracrine signaling with the aldosterone-sensitive distal nephron; and how NaCl reabsorption leads to distal nephron remodeling.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK093501-06
Application #
9264132
Study Section
Special Emphasis Panel (ZRG1-DKUS-J (03))
Program Officer
Ketchum, Christian J
Project Start
2016-09-21
Project End
2021-05-31
Budget Start
2016-09-21
Budget End
2017-05-31
Support Year
6
Fiscal Year
2016
Total Cost
$627,666
Indirect Cost
$119,079
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Welling, Paul A (2018) WNKs on the Fly. J Am Soc Nephrol 29:1347-1349
Harris, Autumn N; Grimm, P Richard; Lee, Hyun-Wook et al. (2018) Mechanism of Hyperkalemia-Induced Metabolic Acidosis. J Am Soc Nephrol 29:1411-1425
Grimm, P Richard; Coleman, Richard; Delpire, Eric et al. (2017) Constitutively Active SPAK Causes Hyperkalemia by Activating NCC and Remodeling Distal Tubules. J Am Soc Nephrol 28:2597-2606
Glykys, Joseph; Dzhala, Volodymyr; Egawa, Kiyoshi et al. (2017) Chloride Dysregulation, Seizures, and Cerebral Edema: A Relationship with Therapeutic Potential. Trends Neurosci 40:276-294
Koumangoye, Rainelli; Delpire, Eric (2017) DNPEP is not the only peptidase that produces SPAK fragments in kidney. Physiol Rep 5:
Shekarabi, Masoud; Zhang, Jinwei; Khanna, Arjun R et al. (2017) WNK Kinase Signaling in Ion Homeostasis and Human Disease. Cell Metab 25:285-299
Welling, Paul A (2016) Roles and Regulation of Renal K Channels. Annu Rev Physiol 78:415-35
Delpire, Eric; Weaver, C David (2016) Challenges of Finding Novel Drugs Targeting the K-Cl Cotransporter. ACS Chem Neurosci 7:1624-1627
Kahle, Kristopher T; Delpire, Eric (2016) Kinase-KCC2 coupling: Cl- rheostasis, disease susceptibility, therapeutic target. J Neurophysiol 115:8-18
Delpire, Eric; Wolfe, Lynne; Flores, Bianca et al. (2016) A patient with multisystem dysfunction carries a truncation mutation in human SLC12A2, the gene encoding the Na-K-2Cl cotransporter, NKCC1. Cold Spring Harb Mol Case Stud 2:a001289

Showing the most recent 10 out of 28 publications