WNK (With No Lysine [K]) kinases comprise a unique branch of the human kinome that appear to be responsible for a wide variety of cellular functions. Mutations of these genes cause human hypertension and have identified them as part of a novel signaling mechanism in the kidney. WNK1, WNK3, and WNK4 have distinct properties to stimulate or inhibit salt transport, effects that can be modified based on physiological need. The WNK signaling complex hypothesis postulates that the kidney specific effects of WNK kinases are mediated by the unique convergence of four members of the WNK kinase family within distal nephron cells. The proposed experiments will elucidate the nature of this complex by demonstrating where the WNK kinases are expressed along the nephron, how WNK3 and WNK4 interact to regulate salt transport, and how a kidney-specific kinase-deficient WNK signals to WNK3 in kidney. It has been demonstrated recently that WNK kinases also mediate aldosterone signaling to the thiazide-sensitive salt transporter. The proposed work will address the mechanisms involved. This work will involve heterologous expression in Xenopus oocytes and epithelial cells.
The second aim will move the work toward more physiologically relevant model systems by examining the effects of increased abundance of the thiazide-sensitive transporter and by developing models to delete or increase expression of WNK kinases specifically along the distal nephron. Specifically, they will test the results of cell-specific knockout or knockin of WNK3. The results will substantially enhance both the understanding of the WNK signaling complex and provide avenues for developing drugs that enhance salt excretion without affecting potassium balance. Project Relevance: Hypertension is the most common disease in the United States. There is a large genetic component, but the nature of the genetic basis is unclear. WNK kinases regulate blood pressure in animals and humans. This work holds the possibility not only of improved understanding of blood pressure regulation but also of developing new, safer and more effective drugs to treat this important disease.

Public Health Relevance

Hypertension is the most common disorder of Americans, accounts for billions of dollars of cost, and costs millions of lives. A large portion of hypertension is related to genetics. This proposal will help unravel genetic contributions to human blood pressure variation, with the goal of finding better treatments, or better preventive maneuvers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK051496-14
Application #
8324679
Study Section
Cellular and Molecular Biology of the Kidney Study Section (CMBK)
Program Officer
Ketchum, Christian J
Project Start
1998-08-01
Project End
2014-03-31
Budget Start
2012-08-01
Budget End
2014-03-31
Support Year
14
Fiscal Year
2012
Total Cost
$228,690
Indirect Cost
$80,190
Name
Oregon Health and Science University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Terker, Andrew S; Yarbrough, Bethzaida; Ferdaus, Mohammed Z et al. (2016) Direct and Indirect Mineralocorticoid Effects Determine Distal Salt Transport. J Am Soc Nephrol 27:2436-45
Hadchouel, Juliette; Ellison, David H; Gamba, Gerardo (2016) Regulation of Renal Electrolyte Transport by WNK and SPAK-OSR1 Kinases. Annu Rev Physiol 78:367-89
Terker, Andrew S; Zhang, Chong; Erspamer, Kayla J et al. (2016) Unique chloride-sensing properties of WNK4 permit the distal nephron to modulate potassium homeostasis. Kidney Int 89:127-34
Zhang, Chong; Meermeier, Nicholas P; Terker, Andrew S et al. (2016) Degradation by Cullin 3 and effect on WNK kinases suggest a role of KLHL2 in the pathogenesis of Familial Hyperkalemic Hypertension. Biochem Biophys Res Commun 469:44-8
Ellison, David H; Terker, Andrew S; Gamba, Gerardo (2016) Potassium and Its Discontents: New Insight, New Treatments. J Am Soc Nephrol 27:981-9
Terker, Andrew S; Ellison, David H (2015) Renal mineralocorticoid receptor and electrolyte homeostasis. Am J Physiol Regul Integr Comp Physiol 309:R1068-70
Terker, Andrew S; Zhang, Chong; McCormick, James A et al. (2015) Potassium modulates electrolyte balance and blood pressure through effects on distal cell voltage and chloride. Cell Metab 21:39-50
Ellison, David H; Terker, Andrew S (2015) Why Your Mother Was Right: How Potassium Intake Reduces Blood Pressure. Trans Am Clin Climatol Assoc 126:46-55
McCormick, James A; Yang, Chao-Ling; Zhang, Chong et al. (2014) Hyperkalemic hypertension-associated cullin 3 promotes WNK signaling by degrading KLHL3. J Clin Invest 124:4723-36
Chávez-Canales, María; Zhang, Chong; Soukaseum, Christelle et al. (2014) WNK-SPAK-NCC cascade revisited: WNK1 stimulates the activity of the Na-Cl cotransporter via SPAK, an effect antagonized by WNK4. Hypertension 64:1047-53

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