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High salt-dependent regulation of the Na+/K+/2Cl- co-transporter (NKCC2) ubiquitination by E3-ubiquitin ligases in Thick Ascending Limb

Award Number: R03DK140261
ORGANIZATION: NATIONAL INSTITUTE OF DIABETES & DIGESTIVE & KIDNEY DISEASES
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 06/12/2025
PERIOD OF PERFORMANCE END DATE: 04/30/2027

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High salt-dependent regulation of the Na+/K+/2Cl- co-transporter (NKCC2) ubiquitination by E3-ubiquitin ligases in Thick Ascending Limb - HYPERTENSION is considered the leading cause of “loss of health” worldwide, involving the kidney’s inability to excrete excess salt. During high salt intake the kidneys excrete the extra salt load by increasing the blood pressure, phenomenon known as the pressure-natriuresis response. On the other hand, salt-sensitive hypertension is a sustained increase in blood pressure caused by an acute salt intake, which is prevalent in 50% of African-Americans and in 30% of Caucasians. Enhanced salt retention by the thick ascending limb of Henle’s loop (TAL) involving the Na+/K+/2Cl- cotransporter (NKCC2) has been described in patients and genetic animal models of salt-sensitive hypertension. However, the molecular mechanism for this defect is not fully understood. Ubiquitination is a post-translational modification that regulates expression of channels and transporters. Recently a novel E3 ubiquitin ligase adaptor F-Box leucine-rich domain 13 (FBXL13) was identified as novel locus for blood pressure regulation in humans. We found that FBXL13 recognizes and interacts with NKCC2. We found that the high salt-induced increase in NKCC2 ubiquitination is blunted in FBXL13-KO mice. Global FBXL13-KO mice show exacerbated total NKCC2 expression. However, the global FBXL13-KO mice show high levels of ubiquitinated NKCC2, indicating that other E3-ubiquitin ligases or adaptors mediates the ubiquitination of NKCC2. Moreover, global FBXL13-KO mice are not salt sensitive, nor they develop hypertension. Therefore, this R03 project aims to discover other E3-ubiquitin ligases that mediates NKCC2 ubiquitination and play a role on NaCl reabsorption and blood pressure regulation under normal or high salt diet. In Aim I, we hypothesize that high salt diet stimulates the 48-linked poli-ubiquitination of NKCC2 via multiple E3-ubiquitin ligases. This proposal is significant to human health because in most hypertensive patients and in animal models of hypertension, the natriuretic effect of nitric oxide is decreased, yet the mechanisms involved in the development of hypertension are poorly understood. Although we already have drugs (loop diuretics) that effectively block NKCC2 activity, they are not used to treat hypertension due to their side effects and offside targets combined with the lose potency over time. This proposal will explore the mechanism and signaling cascade by which high-salt diet stimulates NKCC2 ubiquitination and will characterize a new E3-ubiquitin ligases that may play a critical role in salt-sensitive hypertension. This application will focus on specific interactions between E3-ubiquitin ligases and adaptors with NKCC2. Moreover, this proposal will increase the knowledge on post translational mechanism that regulates blood pressure. The proposal also will help us to understand a post-translational mechanism that we know little about and how it regulates NKCC2 expression, which would be crucial for the development of new strategies for the treatment of hypertension in special salt-sensitive hypertension, which could lead to the development of novel and specific loop diuretics.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2026 ( Subtotal = $115,500 )
2026	2026	WAYNE STATE UNIVERSITY	5700 CASS AVE STE 4900	DETROIT	MI	48202	WAYNE	USA	Diabetes, Digestive, and Kidney Diseases Extramural Research	000	2	5/1/2026	NON-COMPETING CONTINUATION	$115,500
														Subtotal = $115,500

Issue Date FY: 2025 ( Subtotal = $115,500 )
2025	2025	WAYNE STATE UNIVERSITY	5700 CASS AVE STE 4900	DETROIT	MI	48202	WAYNE	USA	Diabetes, Digestive, and Kidney Diseases Extramural Research	000	1	6/11/2025	NEW	$115,500
														Subtotal = $115,500

Grand Total All Awards = $231,000

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High salt-dependent regulation of the Na+/K+/2Cl- co-transporter (NKCC2) ubiquitination by E3-ubiquitin ligases in Thick Ascending Limb

Award Number: R03DK140261

ORGANIZATION: NATIONAL INSTITUTE OF DIABETES & DIGESTIVE & KIDNEY DISEASES

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 06/12/2025

PERIOD OF PERFORMANCE END DATE: 04/30/2027

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