Separate taurine and chloride efflux pathways activated during regulatory v
olume decrease. Am. J. Physiol. 277 (Cell Physiol. 46): C392-C402, 1999.-Or
ganic osmolyte and halide permeability pathways activated in epithelial HeL
a cells by cell swelling were studied by radiotracer efflux techniques and
single-cell volume measurements. The replacement of extracellular Cl- by an
ions that are more permeant through the volume-activated Cl- channel, as in
dicated by electrophysiological measurements, significantly decreased tauri
ne efflux. In the presence of less-permeant anions, an increase in taurine
efflux was observed. Simultaneous measurement of the I-125, used as a trace
r for Cl-, and [H-3]taurine efflux showed that the time courses for the two
effluxes differed. In Cl-rich medium the increase in I- efflux was transie
nt, whereas that for taurine was sustained. Osmosensitive Cl- conductance,
assessed by measuring changes in cell volume, increased rapidly after hypot
onic shock. The influx of taurine was able to counteract Cl- conductance-de
pendent cell shrinkage but only similar to 4 min after triggering cell swel
ling. This taurine-induced effect was blocked by DIDS. Differences in anion
sensitivity, the time course of activation, and sensitivity to DIDS sugges
t that the main cell swelling-activated permeability pathways for taurine a
nd Cl- are separate.