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Review
. 2024 Dec 9:15:1508806.
doi: 10.3389/fphys.2024.1508806. eCollection 2024.

Update on NKCC2 regulation in the thick ascending limb (TAL) by membrane trafficking, phosphorylation, and protein-protein interactions

Affiliations
Review

Update on NKCC2 regulation in the thick ascending limb (TAL) by membrane trafficking, phosphorylation, and protein-protein interactions

Dipak Maskey et al. Front Physiol. .

Abstract

Purpose of review: The thick ascending limb (TAL) of loop of Henle is essential for NaCl, calcium and magnesium homeostasis, pH balance and for urine concentration. NKCC2 is the main transporter for NaCl reabsorption in the TAL and its regulation is very complex. There have been recent advancements toward understanding how NKCC2 is regulated by protein trafficking, protein-protein interaction, and phosphorylation/dephosphorylation. Here, we update the latest molecular mechanisms and players that control NKCC2 function, which gives an increasingly complex picture of NKKC2 regulation in the apical membrane of the TAL.

Recent findings: Protein-protein interactions are required as a regulatory mechanism in many cellular processes. A handful of proteins have been recently identified as an interacting partner of NKCC2, which play major roles in regulating NKCC2 trafficking and activity. New players in NKCC2 internalization and trafficking have been identified. NKCC2 activity is also regulated by kinases and phosphatases, and there have been developments in that area as well.

Summary: Here we review the current understanding of apical trafficking of NKCC2 in the thick ascending limb (TAL) which is tightly controlled by protein-protein interactions, protein turnover and by phosphorylation and dephosphorylation. We discuss new proteins and processes that regulate NKCC2 that have physiological and pathological significance.

Keywords: NKCC2; SLC12A1; protein-protein interactions; proteomics; thick ascending limb.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Molecular mechanism of NKCC2 regulation by trafficking, protein-protein interactions, and phosphorylation at the apical surface of TALs.

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References

    1. Alvarez-Guerra M., Garay R. P. (2002). Renal Na-K-Cl cotransporter NKCC2 in Dahl salt-sensitive rats. J. Hypertens. 20, 721–727. 10.1097/00004872-200204000-00031 - DOI - PubMed
    1. Ares G. R. (2019). cGMP induces degradation of NKCC2 in the thick ascending limb via the ubiquitin-proteasomal system. Am. J. Physiol. Ren. Physiol. 316, F838–f846. 10.1152/ajprenal.00287.2018 - DOI - PubMed
    1. Ares G. R. (2023). Ubiquitination of NKCC2 by the cullin-RING E3 ubiquitin ligase family in the thick ascending limb of the loop of Henle. Am. J. Physiol. Ren. Physiol. 324, F315–f328. 10.1152/ajprenal.00079.2022 - DOI - PMC - PubMed
    1. Ares G. R., Caceres P., Alvarez-Leefmans F. J., Ortiz P. A. (2008). cGMP decreases surface NKCC2 levels in the thick ascending limb: role of phosphodiesterase 2 (PDE2). Am. J. Physiol. Ren. Physiol. 295, F877–F887. 10.1152/ajprenal.00449.2007 - DOI - PMC - PubMed
    1. Ares G. R., Caceres P. S., Ortiz P. A. (2011). Molecular regulation of NKCC2 in the thick ascending limb. Am. J. Physiol. Ren. Physiol. 301, F1143–F1159. 10.1152/ajprenal.00396.2011 - DOI - PMC - PubMed

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