1 The effects of the fluoresceine derivative, phloxine B, on the Cl- curren
t through the cystic fibrosis transmembrane conductance regulator (CFTR) we
re examined in Xenopus oocytes expressing human CFTR.
2 In whole oocytes, the CFTR Cl- current (I-CFTR) was activated by superfus
ion with isobutylmethylxanthine and forskolin. ICFTR was stable during acti
vation and deactivated rapidly upon washout of the activation solution. Phl
oxine B slowed deactivation and, at high concentrations, inhibited ICFTR we
akly.
3 In excised inside-out macroparches, I-CFTR was activated by the catalytic
subunit of protein kinase 4 (cPKA) and MgATP. Phloxine B (0.01-3 mu M), ap
plied after activation, increased ICFTR within 30 s followed by a slow decr
ease which became dominant at high concentrations. Slowing of deactivation
of the CFTR was observed at all concentrations.
4 The effect of phloxine B after 30 s had a bell-shaped concentration-depen
dence with midpoints at 35 and 1600 nM for the stimulatory and the inhibito
ry limb, respectively; maximum stimulation was about 1.8 times. The slow in
hibitory component, measured after 6 min, occurred with an IC50 value of si
milar to 1 mu M.
5 In the absence of cPKA, phloxine B did not stimulate I-CFTR. In the prese
nce of cPKA and MgATP? the effects of phloxine B were more prominent at low
(0.02 mM) than at high ATP (2 mM).
6 The data show that phloxine B modulates ICFTR by increasing channel activ
ity and slowing channel deactivation; at high concentrations inhibition dom
inates. The effects may be mediated by direct interactions with CFTR from t
he inside of the cell.