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1 Department of Physiology and
Biophysics,
We report the characterization of an
Na+/H+
exchanger (NHE) in embryonic fibroblasts (SL-29 cells) of the chicken,
a terrestrial vertebrate, where
Na+ conservation is important.
This exchanger is electroneutral, has a single
Na+ binding site, and is highly
sensitive to amiloride (IC50 2 µM), dimethyl amiloride (350 nM), and ethyl-isopropyl amiloride (25 nM). It is stimulated by serum, transforming growth factor-
, hypertonicity, and okadaic acid. Although these features make it
resemble mammalian NHE1, other characteristics suggest distinct differences. First, in contrast to mammalian NHE1 it is inhibited by
cAMP and shows a biphasic response to phorbol esters and a highly
variable response to increased intracellular
Ca2+ concentration.
Second, whereas full-length human and rat NHE1 cDNA probes recognize a
4.8-kb transcript in rat tissues, they recognize only a 3.9-kb
transcript in chicken tissues. An antibody against amino acids
631-746 of human NHE1 sequence fails to recognize a protein in
SL-29 cells. Rat NHE2 and NHE3 probes do not recognize any transcript
in chicken fibroblasts. The SL-29 exchanger differs markedly from the
previously characterized chicken intestinal apical exchanger in its
amiloride sensitivity and regulation by phorbol esters. These results
suggest that a modified version of mammalian NHE1 is present in chicken
tissues and imply that another functionally distinct
Na+/H+
exchanger is expressed in aves.
SL-29 fibroblasts; sodium/hydrogen exchanger isoform; aves; nonepithelial Na+/H+ antiporter
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