A cell shrinkage-induced non-selective cation conductance with a novel pharmacology in Ehrlich-Lettre-ascites tumour cells.

Research output: Contribution to journalJournal articleResearchpeer-review

  • Peter Lawonn
  • Else K Hoffmann
  • Charlotte Hougaard
  • Frank Wehner
In whole-cell recordings on Ehrlich-Lettre-ascites tumour (ELA) cells, the shrinkage-induced activation of a cation conductance with a selectivity ratio P(Na):P(Li):P(K):P(choline):P(NMDG) of 1.00:0.97:0.88:0.03:0.01 was observed. In order of potency, this conductance was blocked by Gd(3+)=benzamil>amiloride>ethyl-isopropyl-amiloride (EIPA). In patch-clamp studies using the cell-attached configuration, a 14 pS channel became detectable that was reversibly activated upon hypertonic cell shrinkage. It is concluded that ELA cells express a shrinkage-induced cation channel that may reflect a molecular link between amiloride-sensitive and -insensitive channels. In addition, because of its pharmacological profile, it may possibly be related to epithelial Na+ channels (ENaCs).
Original languageEnglish
JournalFEBS Letters
Volume539
Issue number1-3
Pages (from-to)115-9
Number of pages4
ISSN0014-5793
DOIs
Publication statusPublished - 2003

Bibliographical note

Keywords: Animals; Carcinoma, Ehrlich Tumor; Cations; Cell Size; Electric Conductivity; Ion Channels; Patch-Clamp Techniques; Tumor Cells, Cultured

ID: 6768745