BACKGROUND/AIMS: It has been widely accepted that chloride ions moving along chloride channels act to dissipate the electrical gradient established by the electrogenic transport of H(+) ions performed by H(+)-ATPase into subcellular vesicles. Largely known in intracellular compartments, this mechanism is also important at the plasma membrane of cells from various tissues, including kidney. The present work was performed to study the modulation of plasma membrane H(+)-ATPase by chloride channels, in particular, CFTR and ClC-5 in kidney proximal tubule. METHODS AND RESULTS: Using in vivo stationary microperfusion, it was observed that ATPase-mediated HCO(3)(-) reabsorption was significantly reduced in the presence of the Cl(-) channels inhibitor NPPB. This effect was confirmed in vitro by measuring the cell pH recovery rates after a NH(4)Cl pulse in immortalized rat renal proximal tubule cells, IRPTC. In these cells, even after abolishing the membrane potential with valinomycin, ATPase activity was seen to be still dependent on Cl(-). siRNA-mediated CFTR channels and ClC-5 chloride-proton exchanger knockdown significantly reduced H(+)-ATPase activity and V-ATPase B2 subunit expression. CONCLUSION: These results indicate a role of chloride in modulating plasma membrane H(+)-ATPase activity in proximal tubule and suggest that both CFTR and ClC-5 modulate ATPase activity.
BACKGROUND/AIMS: It has been widely accepted that chloride ions moving along chloride channels act to dissipate the electrical gradient established by the electrogenic transport of H(+) ions performed by H(+)-ATPase into subcellular vesicles. Largely known in intracellular compartments, this mechanism is also important at the plasma membrane of cells from various tissues, including kidney. The present work was performed to study the modulation of plasma membrane H(+)-ATPase by chloride channels, in particular, CFTR and ClC-5 in kidney proximal tubule. METHODS AND RESULTS: Using in vivo stationary microperfusion, it was observed that ATPase-mediated HCO(3)(-) reabsorption was significantly reduced in the presence of the Cl(-) channels inhibitor NPPB. This effect was confirmed in vitro by measuring the cell pH recovery rates after a NH(4)Cl pulse in immortalized rat renal proximal tubule cells, IRPTC. In these cells, even after abolishing the membrane potential with valinomycin, ATPase activity was seen to be still dependent on Cl(-). siRNA-mediated CFTR channels and ClC-5chloride-proton exchanger knockdown significantly reduced H(+)-ATPase activity and V-ATPase B2 subunit expression. CONCLUSION: These results indicate a role of chloride in modulating plasma membrane H(+)-ATPase activity in proximal tubule and suggest that both CFTR and ClC-5 modulate ATPase activity.
Authors: Gunnar Dick; Linn K Akslen-Hoel; Frøy Grøndahl; Ingrid Kjos; Kristian Prydz Journal: J Histochem Cytochem Date: 2012-09-01 Impact factor: 2.479
Authors: Ju-Hyun Lee; Devin M Wolfe; Sandipkumar Darji; Mary Kate McBrayer; Daniel J Colacurcio; Asok Kumar; Philip Stavrides; Panaiyur S Mohan; Ralph A Nixon Journal: J Mol Biol Date: 2020-02-24 Impact factor: 5.469
Authors: Anne M Collaco; Peter Geibel; Beth S Lee; John P Geibel; Nadia A Ameen Journal: Am J Physiol Cell Physiol Date: 2013-08-28 Impact factor: 4.249
Authors: José Wilson N Corrêa; Karoline R Boaro; Letícia B Sene; Juliano Z Polidoro; Thiago A Salles; Flavia L Martins; Lusiane M Bendhack; Adriana C C Girardi Journal: Front Physiol Date: 2021-06-09 Impact factor: 4.566
Authors: Adilson Kleber Ferreira; Vanessa Morais Freitas; Débora Levy; Jorge Luiz Mária Ruiz; Sergio Paulo Bydlowski; Rose Eli Grassi Rici; Otaviano Mendonça R Filho; Gilberto Orivaldo Chierice; Durvanei Augusto Maria Journal: PLoS One Date: 2013-03-14 Impact factor: 3.240