Department of Anesthesiology

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Chloride/proton antiporter activity of mammalian CLC proteins ClC-4 and ClC-5.

TitleChloride/proton antiporter activity of mammalian CLC proteins ClC-4 and ClC-5.
Publication TypeJournal Article
Year of Publication2005
AuthorsPicollo A, Pusch M
JournalNature
Volume436
Issue7049
Pagination420-3
Date Published2005 Jul 21
ISSN1476-4687
KeywordsAnimals, Antiporters, Chloride Channels, Chlorides, Electric Conductivity, Humans, Hydrogen-Ion Concentration, Ion Transport, Oocytes, Patch-Clamp Techniques, Protons, Rats, Substrate Specificity
Abstract

ClC-4 and ClC-5 are members of the CLC gene family, with ClC-5 mutated in Dent's disease, a nephropathy associated with low-molecular-mass proteinuria and eventual renal failure. ClC-5 has been proposed to be an electrically shunting Cl- channel in early endosomes, facilitating intraluminal acidification. Motivated by the discovery that certain bacterial CLC proteins are secondary active Cl-/H+ antiporters, we hypothesized that mammalian CLC proteins might not be classical Cl- ion channels but might exhibit Cl(-)-coupled proton transport activity. Here we report that ClC-4 and ClC-5 carry a substantial amount of protons across the plasma membrane when activated by positive voltages, as revealed by measurements of pH close to the cell surface. Both proteins are able to extrude protons against their electrochemical gradient, demonstrating secondary active transport. H+, but not Cl-, transport was abolished when a pore glutamate was mutated to alanine (E211A). ClC-0, ClC-2 and ClC-Ka proteins showed no significant proton transport. The muscle channel ClC-1 exhibited a small H+ transport that might be physiologically relevant. For ClC-5, we estimated that Cl- and H+ transport contribute about equally to the total charge movement, raising the possibility that the coupled Cl-/H+ transport of ClC-4 and ClC-5 is of significant magnitude in vivo.

DOI10.1038/nature03720
Alternate JournalNature
PubMed ID16034421
Grant ListGGP04018 / / Telethon / Italy