ACELL September 46/3

نویسندگان

  • V. SEPÚLVEDA
  • Rubén Torres
  • Macarena Oporto
  • Patricio Pacheco
  • Ana Luisa Eguiguren
  • L. Pablo Cid
چکیده

Stutzin, Andrés, Rubén Torres, Macarena Oporto, Patricio Pacheco, Ana Luisa Eguiguren, L. Pablo Cid, and Francisco V. Sepúlveda. Separate taurine and chloride efflux pathways activated during regulatory volume decrease. Am. J. Physiol. 277 (Cell Physiol. 46): C392–C402, 1999.—Organic osmolyte and halide permeability pathways activated in epithelial HeLa cells by cell swelling were studied by radiotracer efflux techniques and single-cell volume measurements. The replacement of extracellular Cl2 by anions that are more permeant through the volume-activated Cl2 channel, as indicated by electrophysiological measurements, significantly decreased taurine efflux. In the presence of less-permeant anions, an increase in taurine efflux was observed. Simultaneous measurement of the 125I, used as a tracer for Cl2, and [3H]taurine efflux showed that the time courses for the two effluxes differed. In Cl2-rich medium the increase in I2 efflux was transient, whereas that for taurine was sustained. Osmosensitive Cl2 conductance, assessed by measuring changes in cell volume, increased rapidly after hypotonic shock. The influx of taurine was able to counteract Cl2 conductance-dependent cell shrinkage but only ,4 min after triggering cell swelling. This taurine-induced effect was blocked by DIDS. Differences in anion sensitivity, the time course of activation, and sensitivity to DIDS suggest that the main cell swelling-activated permeability pathways for taurine and Cl2 are separate.

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تاریخ انتشار 1999