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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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cites | cdi_FETCH-LOGICAL-c1881-1ce26380e143cf336fd4428bfb2f62bcc2f2fb56fd07372b731da3d9f2b067593 |
container_end_page | 156 |
container_issue | 1 |
container_start_page | 152 |
container_title | FEBS letters |
container_volume | 521 |
creator | Lemonnier, L Vitko, Y Shuba, Y.M Vanden Abeele, F Prevarskaya, N Skryma, R |
description | 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. |
doi_str_mv | 10.1016/S0014-5793(02)02863-6 |
format | article |
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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.</description><identifier>ISSN: 0014-5793</identifier><identifier>EISSN: 1873-3468</identifier><identifier>DOI: 10.1016/S0014-5793(02)02863-6</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>BAPTA ; Calcium chelating agent ; EDTA ; Life Sciences ; LNCaP prostate cancer cell ; Swelling-activated chloride current ; Volume-regulated anion channel</subject><ispartof>FEBS letters, 2002-06, Vol.521 (1), p.152-156</ispartof><rights>2002</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1881-1ce26380e143cf336fd4428bfb2f62bcc2f2fb56fd07372b731da3d9f2b067593</citedby><cites>FETCH-LOGICAL-c1881-1ce26380e143cf336fd4428bfb2f62bcc2f2fb56fd07372b731da3d9f2b067593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014579302028636$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,45759</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04321597$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lemonnier, L</creatorcontrib><creatorcontrib>Vitko, Y</creatorcontrib><creatorcontrib>Shuba, Y.M</creatorcontrib><creatorcontrib>Vanden Abeele, F</creatorcontrib><creatorcontrib>Prevarskaya, N</creatorcontrib><creatorcontrib>Skryma, R</creatorcontrib><title>Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents</title><title>FEBS letters</title><description>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.</description><subject>BAPTA</subject><subject>Calcium chelating agent</subject><subject>EDTA</subject><subject>Life Sciences</subject><subject>LNCaP prostate cancer cell</subject><subject>Swelling-activated chloride current</subject><subject>Volume-regulated anion channel</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEUhYMoWKs_QcjSItE8ZjKZlZT6qFB0oa5DkrlpR6aJTKaF_ntnWunW1eWee86B-yF0zegdo0zef1DKMpIXpbihfEK5koLIEzRiqhBEZFKdotHRco4uUvqm_a5YOUJvj3ULrsPrWG0a09Ux4OjxNjabNZAWloMIFTZhuLiVCQGahO0Ozwzmt70CQyossVlC6NIlOvOmSXD1N8fo6_npczYni_eX19l0QRxTihHmgEuhKLBMOC-E9FWWcWW95V5y6xz33Nu8l2khCm4LwSojqtJzS2WRl2KMJofelWn0T1uvTbvT0dR6Pl3oQaOZ4Cwviy3rvfnB69qYUgv-GGBUDwD1HqAe6GjK9R6gln3u4ZDrP4ZtDa1OrobgoNoj01Ws_2n4BaITdq4</recordid><startdate>20020619</startdate><enddate>20020619</enddate><creator>Lemonnier, L</creator><creator>Vitko, Y</creator><creator>Shuba, Y.M</creator><creator>Vanden Abeele, F</creator><creator>Prevarskaya, N</creator><creator>Skryma, R</creator><general>Elsevier B.V</general><general>Wiley</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope></search><sort><creationdate>20020619</creationdate><title>Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents</title><author>Lemonnier, L ; Vitko, Y ; Shuba, Y.M ; Vanden Abeele, F ; Prevarskaya, N ; Skryma, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1881-1ce26380e143cf336fd4428bfb2f62bcc2f2fb56fd07372b731da3d9f2b067593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>BAPTA</topic><topic>Calcium chelating agent</topic><topic>EDTA</topic><topic>Life Sciences</topic><topic>LNCaP prostate cancer cell</topic><topic>Swelling-activated chloride current</topic><topic>Volume-regulated anion channel</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lemonnier, L</creatorcontrib><creatorcontrib>Vitko, Y</creatorcontrib><creatorcontrib>Shuba, Y.M</creatorcontrib><creatorcontrib>Vanden Abeele, F</creatorcontrib><creatorcontrib>Prevarskaya, N</creatorcontrib><creatorcontrib>Skryma, R</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lemonnier, L</au><au>Vitko, Y</au><au>Shuba, Y.M</au><au>Vanden Abeele, F</au><au>Prevarskaya, N</au><au>Skryma, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents</atitle><jtitle>FEBS letters</jtitle><date>2002-06-19</date><risdate>2002</risdate><volume>521</volume><issue>1</issue><spage>152</spage><epage>156</epage><pages>152-156</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>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.</abstract><pub>Elsevier B.V</pub><doi>10.1016/S0014-5793(02)02863-6</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | FEBS letters, 2002-06, Vol.521 (1), p.152-156 |
issn | 0014-5793 1873-3468 |
language | eng |
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source | ScienceDirect®; Wiley-Blackwell Read & Publish Collection |
subjects | BAPTA Calcium chelating agent EDTA Life Sciences LNCaP prostate cancer cell Swelling-activated chloride current Volume-regulated anion channel |
title | Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents |
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