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Article: Regulation of human cardiac KCNQ1/KCNE1 channel by epidermal growth factor receptor kinase
Title | Regulation of human cardiac KCNQ1/KCNE1 channel by epidermal growth factor receptor kinase | ||||
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Authors | |||||
Keywords | Electrophysiology Epidermal growth factor receptor kinase Protein tyrosine phosphorylation Recombinant cardiac hKCNQ1/hKCNE1 channel | ||||
Issue Date | 2010 | ||||
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/bbamem | ||||
Citation | Biochimica Et Biophysica Acta - Biomembranes, 2010, v. 1798 n. 5, p. 995-1001 How to Cite? | ||||
Abstract | The aim of the present study was to investigate whether/how the recombinant human cardiac I Ks could be regulated by epidermal growth factor receptor kinase in HEK 293 cells stably expressing hKCNQ1/hKCNE1 genes using the approaches of perforated patch clamp technique, immunoprecipitation and Western blot analysis. It was found that the broad spectrum isoflavone tyrosine kinase inhibitor genistein and the selective epidermal growth factor receptor kinase inhibitor tyrphostin AG556 suppressed the recombinant I Ks, and their inhibition was countered by the protein tyrosine phosphatase inhibitor orthovanadate. The Src-family kinase inhibitor PP2 reduced the current, but the effect was not antagonized by orthovanadate. Immunoprecipitation and Western blot analysis revealed that tyrosine phosphorylation level of hKCNQ1 protein was decreased by genistein or AG556, but not by PP2. These results provide the novel information that epidermal growth factor receptor kinase, but not Src-family kinases, regulates the recombinant cardiac I Ks stably expressed in HEK 293 cells via phosphorylating KCNQ1 protein of the channel. © 2009 Elsevier B.V. All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/77635 | ||||
ISSN | 2023 Impact Factor: 2.8 2023 SCImago Journal Rankings: 0.947 | ||||
ISI Accession Number ID |
Funding Information: The study was supported by a grant from Sun Chieh Yeh Heart Foundation of Hong Kong. The authors thank Mr. Wentao Li for the critical reading of the manuscript. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Dong, MQ | en_HK |
dc.contributor.author | Sun, HY | en_HK |
dc.contributor.author | Tang, Q | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.contributor.author | Lau, CP | en_HK |
dc.contributor.author | Li, GR | en_HK |
dc.date.accessioned | 2010-09-06T07:34:03Z | - |
dc.date.available | 2010-09-06T07:34:03Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Biochimica Et Biophysica Acta - Biomembranes, 2010, v. 1798 n. 5, p. 995-1001 | en_HK |
dc.identifier.issn | 0005-2736 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77635 | - |
dc.description.abstract | The aim of the present study was to investigate whether/how the recombinant human cardiac I Ks could be regulated by epidermal growth factor receptor kinase in HEK 293 cells stably expressing hKCNQ1/hKCNE1 genes using the approaches of perforated patch clamp technique, immunoprecipitation and Western blot analysis. It was found that the broad spectrum isoflavone tyrosine kinase inhibitor genistein and the selective epidermal growth factor receptor kinase inhibitor tyrphostin AG556 suppressed the recombinant I Ks, and their inhibition was countered by the protein tyrosine phosphatase inhibitor orthovanadate. The Src-family kinase inhibitor PP2 reduced the current, but the effect was not antagonized by orthovanadate. Immunoprecipitation and Western blot analysis revealed that tyrosine phosphorylation level of hKCNQ1 protein was decreased by genistein or AG556, but not by PP2. These results provide the novel information that epidermal growth factor receptor kinase, but not Src-family kinases, regulates the recombinant cardiac I Ks stably expressed in HEK 293 cells via phosphorylating KCNQ1 protein of the channel. © 2009 Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/bbamem | en_HK |
dc.relation.ispartof | Biochimica et Biophysica Acta - Biomembranes | en_HK |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in Biochimica et Biophysica Acta (BBA) - Biomembranes. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Biochimica et Biophysica Acta (BBA) - Biomembranes, 2010, v. 1798 n. 5, p. 995-1001. DOI: http://dx.doi.org/10.1016/j.bbamem.2010.01.010 | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Electrophysiology | en_HK |
dc.subject | Epidermal growth factor receptor kinase | en_HK |
dc.subject | Protein tyrosine phosphorylation | en_HK |
dc.subject | Recombinant cardiac hKCNQ1/hKCNE1 channel | en_HK |
dc.subject.mesh | Cell Line | - |
dc.subject.mesh | Electrophysiology | - |
dc.subject.mesh | KCNQ1 Potassium Channel - genetics - metabolism | - |
dc.subject.mesh | Receptor, Epidermal Growth Factor - antagonists and inhibitors - genetics - metabolism | - |
dc.subject.mesh | Recombinant Proteins - genetics - metabolism | - |
dc.title | Regulation of human cardiac KCNQ1/KCNE1 channel by epidermal growth factor receptor kinase | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0005-2736&volume=1798&issue=5&spage=995&epage=1001&date=2010&atitle=Regulation+of+human+cardiac+KCNQ1/KCNE1+channel+by+epidermal+growth+factor+receptor+kinase | en_HK |
dc.identifier.email | Tse, HF:hftse@hkucc.hku.hk | en_HK |
dc.identifier.email | Li, GR:grli@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tse, HF=rp00428 | en_HK |
dc.identifier.authority | Li, GR=rp00476 | en_HK |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/j.bbamem.2010.01.010 | en_HK |
dc.identifier.pmid | 20085748 | - |
dc.identifier.scopus | eid_2-s2.0-77949263580 | en_HK |
dc.identifier.hkuros | 168824 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77949263580&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 1798 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 995 | en_HK |
dc.identifier.epage | 1001 | en_HK |
dc.identifier.isi | WOS:000276648800015 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Dong, MQ=7202127303 | en_HK |
dc.identifier.scopusauthorid | Sun, HY=35723049200 | en_HK |
dc.identifier.scopusauthorid | Tang, Q=40861778800 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.scopusauthorid | Lau, CP=7401968501 | en_HK |
dc.identifier.scopusauthorid | Li, GR=7408462932 | en_HK |
dc.identifier.issnl | 0005-2736 | - |