Manganese promotes intracellular accumulation of AQP2 via modulating f-actin polymerization and reduces urinary concentration in mice

Lei Lei, Ming Huang, Limin Su, Dongping Xie, Fahmy A. Mamuya, Onju Ham, Kenji Tsuji, Teodor G. Păunescu, Baoxue Yang, Hua A.Jenny Lu

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Aquaporin-2 (AQP2) is a water channel protein expressed in principal cells (PCs) of the kidney collecting ducts (CDs) and plays a critical role in mediating water reabsorption and urine concentration. AQP2 undergoes both regulated trafficking mediated by vasopressin (VP) and constitutive recycling, which is independent of VP. For both pathways, actin cytoskeletal dynamics is a key determinant of AQP2 trafficking. We report here that manganese chloride (MnCl2) is a novel and potent regulator of AQP2 trafficking in cultured cells and in the kidney. MnCl2 treatment promoted internalization and intracellular accumulation of AQP2. The effect of MnCl2 on the intracellular accumulation of AQP2 was associated with activation of RhoA and actin polymerization without modification of AQP2 phosphorylation. Although the level of total and phosphorylated AQP2 did not change, MnCl2 treatment impeded VP-induced phosphorylation of AQP2 at its serine-256, -264, and -269 residues and dephosphorylation at serine 261. In addition, MnCl2 significantly promoted F-actin polymerization along with downregulation of RhoA activity and prevented VP-induced membrane accumulation of AQP2. Finally, MnCl2 treatment in mice resulted in significant polyuria and reduced urinary concentration, likely due to intracellular relocation of AQP2 in the PCs of kidney CDs. More importantly, the reduced urinary concentration caused by MnCl2 treatment in animals was not corrected by VP. In summary, our study identified a novel effect of MnCl2 on AQP2 trafficking through modifying RhoA activity and actin polymerization and uncovered its potent impact on water diuresis in vivo.

Original languageEnglish
Pages (from-to)F306-F316
JournalAmerican Journal of Physiology - Renal Physiology
Volume314
Issue number2
DOIs
Publication statusPublished - Feb 1 2018
Externally publishedYes

Keywords

  • Aquaporin-2
  • Endocytosis
  • Manganese
  • Urine concentration

ASJC Scopus subject areas

  • Physiology
  • Urology

Fingerprint Dive into the research topics of 'Manganese promotes intracellular accumulation of AQP2 via modulating f-actin polymerization and reduces urinary concentration in mice'. Together they form a unique fingerprint.

  • Cite this