Role of CFTR and ClC-5 in Modulating Vacuolar H+-ATPase Activity in Kidney Proximal Tubule

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 i...

Descripción completa

Detalles Bibliográficos
Autores: Carraro-Lacroix, Luciene Regina [UNIFESP], Lessa, Lucilia M. A., Bezerra, Camila N. A., Pessoa, Thaissa D., Souza-Menezes, Jackson, Morales, Marcelo M., Girardi, Adriana C. C., Malnic, Gerhard
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2010
País:Brasil
Institución:Universidade Federal de São Paulo (UNIFESP)
Repositorio:Repositório Institucional da UNIFESP
Idioma:inglés
OAI Identifier:oai:repositorio.unifesp.br:11600/32041
Acceso en línea:http://dx.doi.org/10.1159/000322324
http://repositorio.unifesp.br/handle/11600/32041
Access Level:acceso abierto
Palabra clave:H+-ATPase
Chloride
CFTR
ClC-5
Proximal tubule
Descripción
Sumario: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 HCO3- 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 NH4Cl 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. Copyright (C) 2010 S. Karger AG, Basel