NRBP1 and TSC22D proteins affect distal convoluted tubule physiology through modulation of the WNK pathway
Year: 2025
Type: article
Abstract: The with-no-lysine (K) (WNK) kinases regulate processes such as cell volume and epithelial ion transport through the modulation of cation chloride cotransporters such as the NaCl cotransporter (NCC) present in the distal convoluted tubule (DCT) of the kidney. Recently, the interaction of WNKs with nuclear receptor binding protein 1 (NRBP1) and transforming growth factor–β–stimulated clone 22 domain (TSC22D) proteins was reported. Here, we explored the effect of NRBP1 and TSC22Ds on WNK signaling in vitro and in the DCT. TSC22D1.1, TSC22D2, and NRBP1 are localized in DCT WNK bodies, which are cytoplasmic biomolecular condensates associated with WNK activation. In HEK293 cells, long TSC22D isoforms and NRBP1 increase WNK4 activity. DCT-specific NRBP1-knockout mice have reduced NCC phosphorylation and activate a compensatory response. Thus, NRBP1 and long TSC22D proteins are positive modulators of WNK signaling and modulate Na + reabsorption in the kidney. NRBP1 and TSC22Ds likely influence WNK signaling in other tissues, affecting various physiological processes.
Source: Science Advances
Authors: Germán Magaña-Ávila, Héctor Carbajal-Contreras, Ramchandra V. Amnekar, Toby Dite, Michelle Téllez-Sutterlin, Kevin García-Ávila, Brenda Marquina-Castillo, Alejandro Lopez-Saavedra, Norma Vazquez, Eréndira Rojas-Ortega, Eric Delpire, David H. Ellison, Dario R. Alessi, Gerardo Gamba, María Castañeda-Bueno
Institutions: Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Universidad Nacional Autónoma de México, University of Dundee, MRC Protein Phosphorylation and Ubiquitylation Unit, Instituto Nacional de Cancerología, Tecnológico de Monterrey, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Vanderbilt University, Oregon Health & Science University, VA Portland Health Care System
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $4,500
OpenAlex ID: W4412483202
