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


Autoria(s): CARRARO-LACROIX, Luciene R.; LESSA, Lucilia M. A.; BEZERRA, Camila N. A.; PESSOA, Thaissa D.; SOUZA-MENEZES, Jackson; MORALES, Marcelo M.; GIRARDI, Adriana C. C.; MALNIC, Gerhard
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

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. Copyright (C) 2010 S. Karger AG, Basel

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/01683-5]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[05/60491-1]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[06/50828-1]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[07/52945-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[09/51772-8]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)[304855/2006-5]

Identificador

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, v.26, n.4/Mai, p.563-576, 2010

1015-8987

http://producao.usp.br/handle/BDPI/28054

10.1159/000322324

http://dx.doi.org/10.1159/000322324

Idioma(s)

eng

Publicador

KARGER

Relação

Cellular Physiology and Biochemistry

Direitos

restrictedAccess

Copyright KARGER

Palavras-Chave #H(+)-ATPase #Chloride #CFTR #ClC-5 #Proximal tubule #RECEPTOR-MEDIATED ENDOCYTOSIS #MALE REPRODUCTIVE-TRACT #CHLORIDE CHANNEL #DENTS-DISEASE #PROTON SECRETION #CYSTIC-FIBROSIS #BICARBONATE ABSORPTION #IMPAIRS ENDOCYTOSIS #NA+/H+ EXCHANGER #BONE-RESORPTION #Cell Biology #Physiology
Tipo

article

original article

publishedVersion