Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 285, Issue 4, Pages 2569-2579Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M109.018002
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Funding
- National Institutes of Health [R01 HL62483, T32 DK07690-15]
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Adenovirus expressing ClC-3 (Ad-ClC-3) induces Cl-/H+ antiportcurrent (IClC-3) in HEK293 cells. The outward rectification and time dependence of IClC-3 closely resemble an endogenous HEK293 cell acid-activated Cl- current (IClacid) seen at extracellular pH <= 5.5. IClacid was present in smooth muscle cells from wildtype but not ClC-3 null mice. We therefore sought to determine whether these currents were related. IClacid was larger in cells expressing Ad-ClC-3. Protons shifted the reversal potential (E-rev) of IClC-3 between pH 8.2 and 6.2, but not pH 6.2 and 5.2, suggesting that Cl- and H+ transport become uncoupled at low pH. At pH 4.0 E-rev was completely Cl- dependent (55.8 +/- 2.3 mV/decade). Several findings linked ClC-3 with native IClacid; 1) RNA interference directed at ClC-3 message reduced native IClacid; 2) removal of the extracellular fast gate (E224A) produced large currents that were pH-insensitive; and 3) wild-type IClC-3 and IClacid were both inhibited by (2-sulfonatoethyl) methanethiosulfonate (MTSES; 10-500 mu M)-induced alkanethiolation at exposed cysteine residues. However, a ClC-3 mutant lacking four extracellular cysteine residues (C103_P130del) was completely resistant to MTSES. C103_P130del currents were still acid-activated, but could be distinguished from wild-type IClC-3 and from native IClacid by a much slower response to low pH. Thus, ClC-3 currents are activated by protons and ClC-3 protein may account for native IClacid. Low pH uncouples Cl-/H+ transport so that at pH 4.0 ClC-3 behaves as an anion-selective channel. These findings have important implications for the biology of Cl-/H+ antiporters and perhaps for pH regulation in highly acidic intracellular compartments.
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