To determine whether NG108-15 cells contain a functional Na+/Ca2+ exch
anger, we isotonically replaced extracellular Na+ with N-methyl-D-gluc
amine (NMG) and measured the effect on cytosolic Ca2+ concentration ([
Ca2+](i)) using the fluorescent Ca2+ indicator fura 2. Replacement wit
h NMG alone had no effect on basal [Ca2+](i) or the rise in [Ca2+](i)
evoked by 80 mM K+ or 10 mu M bradykinin, but caused a larger [Ca2+](i
) increase when thapsigargin and carbonyl cyanide p-trifluoromethoxyph
enylhydrazone (FCCP) were added to the cells; this enhanced [Ca2+](i)
increase could be reversed by adding Na+ back to the bathing buffer. T
he elevation in [Ca2+](i) induced by thapsigargin and FCCP was inverse
ly proportional to extracellular Na+ concentration. Furthermore, the e
xchanger operated in the reverse mode, as measured by either [Ca2+](i)
change or Ca-45(2+) uptake. An 810 bp cDNA fragment of the exchanger
was amplified by PCR; it differed by a single amino acid residue from
the corresponding segment of the rat brain Na+/Ca2+ exchanger. These d
ata suggest that a functioning Na+/Ca2+ exchanger exists in NG108-15 c
ells.