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J Biol Chem
2020 Feb 07;2956:1464-1473. doi: 10.1074/jbc.RA119.011366.
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Cl- and H+ coupling properties and subcellular localizations of wildtype and disease-associated variants of the voltage-gated Cl-/H+ exchanger ClC-5.
Chang MH
,
Brown MR
,
Liu Y
,
Gainullin VG
,
Harris PC
,
Romero MF
,
Lieske JC
.
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Dent disease 1 (DD1) is caused by mutations in the CLCN5 gene encoding a voltage-gated electrogenic nCl-/H+ exchanger ClC-5. Using ion-selective microelectrodes and Xenopus oocytes, here we studied Cl-/H+ coupling properties of WT ClC-5 and four DD1-associated variants (S244L, R345W, Q629*, and T657S), along with trafficking and localization of ClC-5. WT ClC-5 had a 2Cl-/H+ exchange ratio at a Vh of +40 mV with a [Cl-]out of 104 mm, but the transport direction did not reverse with a [Cl-]out of 5 mm, indicating that ClC-5-mediated exchange of two Cl- out for one H+ in is not permissible. We hypothesized that ClC-5 and H+-ATPase are functionally coupled during H+-ATPase-mediated endosomal acidification, crucial for ClC-5 activation by depolarizing endosomes. ClC-5 transport that provides three net negative charges appeared self-inhibitory because of ClC-5's voltage-gated properties, but shunt conductance facilitated further H+-ATPase-mediated endosomal acidification. Thus, an on-and-off "burst" of ClC-5 activity was crucial for preventing Cl- exit from endosomes. The subcellular distribution of the ClC-5:S244L variant was comparable with that of WT ClC-5, but the variant had a much slower Cl- and H+ transport and displayed an altered stoichiometry of 1.6:1. The ClC-5:R345W variant exhibited slightly higher Cl-/H+ transport than ClC-5:S244L, but co-localized with early endosomes, suggesting decreased ClC-5:R345W membrane trafficking is perhaps in a fully functional form. The truncated ClC-5:Q629* variant displayed the lowest Cl-/H+ exchange and was retained in the endoplasmic reticulum and cis-Golgi, but not in early endosomes, suggesting the nonsense mutation affects ClC-5 maturation and trafficking.
Accardi,
Synergism between halide binding and proton transport in a CLC-type exchanger.
2006, Pubmed
Accardi,
Synergism between halide binding and proton transport in a CLC-type exchanger.
2006,
Pubmed
Accardi,
Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels.
2004,
Pubmed
Bignon,
A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification.
2018,
Pubmed
,
Xenbase
Bregestovski,
Genetically encoded optical sensors for monitoring of intracellular chloride and chloride-selective channel activity.
2009,
Pubmed
Brown,
Regulation of the V-ATPase in kidney epithelial cells: dual role in acid-base homeostasis and vesicle trafficking.
2009,
Pubmed
Chang,
Entry to "formula tunnel" revealed by SLC4A4 human mutation and structural model.
2008,
Pubmed
,
Xenbase
Claverie-Martín,
Dent's disease: clinical features and molecular basis.
2011,
Pubmed
Devuyst,
Dent's disease.
2010,
Pubmed
Devuyst,
Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease.
1999,
Pubmed
Dutzler,
X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.
2002,
Pubmed
Feng,
Structure of a eukaryotic CLC transporter defines an intermediate state in the transport cycle.
2010,
Pubmed
Forgac,
The vacuolar H+-ATPase of clathrin-coated vesicles is reversibly inhibited by S-nitrosoglutathione.
1999,
Pubmed
Gluck,
The role of the V-ATPase in renal epithelial H+ transport.
1992,
Pubmed
Grand,
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.
2009,
Pubmed
,
Xenbase
Günther,
The ClC-5 chloride channel knock-out mouse - an animal model for Dent's disease.
2003,
Pubmed
Günther,
ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells.
1998,
Pubmed
Hara-Chikuma,
Impaired acidification in early endosomes of ClC-5 deficient proximal tubule.
2005,
Pubmed
Hryciw,
The interaction between megalin and ClC-5 is scaffolded by the Na⁺-H⁺ exchanger regulatory factor 2 (NHERF2) in proximal tubule cells.
2012,
Pubmed
Igarashi,
Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
1998,
Pubmed
,
Xenbase
Jentsch,
CLC chloride channels and transporters.
2005,
Pubmed
Ludewig,
Two physically distinct pores in the dimeric ClC-0 chloride channel.
1996,
Pubmed
,
Xenbase
Ludwig,
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalization.
2005,
Pubmed
,
Xenbase
Middleton,
Homodimeric architecture of a ClC-type chloride ion channel.
1996,
Pubmed
Modi,
Two DNA nanomachines map pH changes along intersecting endocytic pathways inside the same cell.
2013,
Pubmed
Nauli,
Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction.
2006,
Pubmed
Nguitragool,
Uncoupling of a CLC Cl-/H+ exchange transporter by polyatomic anions.
2006,
Pubmed
Novarino,
Endosomal chloride-proton exchange rather than chloride conductance is crucial for renal endocytosis.
2010,
Pubmed
Ohshima,
Donnan potential and surface potential of a charged membrane.
1985,
Pubmed
Picollo,
Chloride/proton antiporter activity of mammalian CLC proteins ClC-4 and ClC-5.
2005,
Pubmed
Piwon,
ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.
2000,
Pubmed
Pusch,
ClC-5: Physiological role and biophysical mechanisms.
2015,
Pubmed
Romero,
Cloning and characterization of a Na+-driven anion exchanger (NDAE1). A new bicarbonate transporter.
2000,
Pubmed
,
Xenbase
Saha,
A pH-independent DNA nanodevice for quantifying chloride transport in organelles of living cells.
2015,
Pubmed
Sakamoto,
Cellular and subcellular immunolocalization of ClC-5 channel in mouse kidney: colocalization with H+-ATPase.
1999,
Pubmed
Salomonsson,
The cytosolic chloride concentration in macula densa and cortical thick ascending limb cells.
1993,
Pubmed
Satoh,
Functional coupling of V-ATPase and CLC-5.
2017,
Pubmed
Scheel,
Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins.
2005,
Pubmed
,
Xenbase
Sciortino,
Cation and voltage dependence of rat kidney electrogenic Na(+)-HCO(-)(3) cotransporter, rkNBC, expressed in oocytes.
1999,
Pubmed
,
Xenbase
Sonawane,
Determinants of [Cl-] in recycling and late endosomes and Golgi complex measured using fluorescent ligands.
2003,
Pubmed
Sonawane,
Chloride concentration in endosomes measured using a ratioable fluorescent Cl- indicator: evidence for chloride accumulation during acidification.
2002,
Pubmed
Steinmeyer,
Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease.
1995,
Pubmed
,
Xenbase
Sun-Wada,
Vacuolar-type proton pump ATPases: acidification and pathological relationships.
2013,
Pubmed
Tanaka,
Cytosolic Cl- Affects the Anticancer Activity of Paclitaxel in the Gastric Cancer Cell Line, MKN28 Cell.
2017,
Pubmed
Tang,
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients.
2016,
Pubmed
Tanuma,
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.
2007,
Pubmed
,
Xenbase
Vandewalle,
Tissue distribution and subcellular localization of the ClC-5 chloride channel in rat intestinal cells.
2001,
Pubmed
Walden,
Uncoupling and turnover in a Cl-/H+ exchange transporter.
2007,
Pubmed
Wang,
Glomerular Pathology in Dent Disease and Its Association with Kidney Function.
2016,
Pubmed
Wang,
Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis.
2000,
Pubmed
Weinreich,
Pores formed by single subunits in mixed dimers of different CLC chloride channels.
2001,
Pubmed
Yamamoto,
Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.
2000,
Pubmed
,
Xenbase
Zdebik,
Determinants of anion-proton coupling in mammalian endosomal CLC proteins.
2008,
Pubmed
Zifarelli,
Conversion of the 2 Cl(-)/1 H+ antiporter ClC-5 in a NO3(-)/H+ antiporter by a single point mutation.
2009,
Pubmed
,
Xenbase
Zifarelli,
Intracellular regulation of human ClC-5 by adenine nucleotides.
2009,
Pubmed