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Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents
Ca 2+ chelating agents are widely used in biological research for Ca 2+ buffering. Here we report that BAPTA, EDTA and HEDTA produce fast, reversible, voltage-dependent inhibition of swelling-activated Cl − current ( I Cl,swell) in LNCaP prostate cancer epithelial cells that is unrelated to their Ca...
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Published in: | FEBS letters 2002-06, Vol.521 (1), p.152-156 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ca
2+ chelating agents are widely used in biological research for Ca
2+ buffering. Here we report that BAPTA, EDTA and HEDTA produce fast, reversible, voltage-dependent inhibition of swelling-activated Cl
− current (
I
Cl,swell) in LNCaP prostate cancer epithelial cells that is unrelated to their Ca
2+ binding. BAPTA was the most effective (maximal blockade 67%, IC
50=70 μM, at +100 mV) followed by EDTA and HEDTA.
I
Cl,swell blockade by EDTA was pH-dependent. BAPTA blocked
I
Cl,swell also in other cell types. We conclude that Ca
2+ chelating agents block
I
Cl,swell by acting directly on the underlying channel, and that the negative charge of the free chelator form is critical for the blockade. |
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ISSN: | 0014-5793 1873-3468 |
DOI: | 10.1016/S0014-5793(02)02863-6 |