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1 Department of Pediatrics,
Our objective in
this study was to determine the effect of changes in luminal and
cytoplasmic pH on cystic fibrosis transmembrane regulator (CFTR)
Cl
conductance
(GCl). We
monitored CFTR
GCl in the apical
membranes of sweat ducts as reflected by
Cl
diffusion potentials
(VCl) and
transepithelial conductance
(GCl). We found
that luminal pH (5.0-8.5) had little effect on the
cAMP/ATP-activated CFTR
GCl, showing that
CFTR GCl is
maintained over a broad range of extracellular pH in which it functions
physiologically. However, we found that phosphorylation activation of
CFTR GCl is
sensitive to intracellular pH. That is, in the presence of cAMP and ATP [adenosine
5'-O-(3-thiotriphosphate)],
CFTR could be phosphorylated at physiological pH (6.8) but not at low
pH (~5.5). On the other hand, basic pH prevented endogenous
phosphatase(s) from dephosphorylating CFTR.After phosphorylation
of CFTR with cAMP and ATP, CFTR
GCl is normally
deactivated within 1 min after cAMP is removed, even in the presence of
5 mM ATP. This deactivation was due to an increase in endogenous
phosphatase activity relative to kinase activity, since it was reversed
by the reapplication of ATP and cAMP. However, increasing cytoplasmic
pH significantly delayed the deactivation of CFTR
GCl in a
dose-dependent manner, indicating inhibition of dephosphorylation. We
conclude that CFTR
GCl may be
regulated via shifts in cytoplasmic pH that mediate reciprocal control
of endogenous kinase and phosphatase activities. Luminal pH probably has little direct effect on these mechanisms. This regulation of CFTR
may be important in shifting electrolyte transport in the duct from
conductive to nonconductive modes.
sweat duct; phosphatase; kinase; chloride transport; chloride conductance; fluid transport; electrolyte transport; sweat gland; cystic fibrosis
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