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- Publisher Website: 10.1152/ajpcell.00240.2007
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- PMID: 17699636
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Article: Functional ion channels in mouse bone marrow mesenchymal stem cells
Title | Functional ion channels in mouse bone marrow mesenchymal stem cells |
---|---|
Authors | |
Keywords | Intermediate-conductance calcium-activated potassium current Inward rectifier potassium current Volume-sensitive chloride current |
Issue Date | 2007 |
Publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpcell.physiology.org/ |
Citation | American Journal Of Physiology - Cell Physiology, 2007, v. 293 n. 5, p. C1561-C1567 How to Cite? |
Abstract | Bone marrow mesenchymal stem cells (MSCs) are used as a cell source for cardiomyoplasty; however, the cellular electrophysiological properties are not fully understood. The present study was to investigate the functional ionic channels in undifferentiated mouse bone marrow MSCs using whole cell patch-voltage clamp technique, RT-PCR, and Western immunoblotting analysis. We found that three types of ionic currents were present in mouse MSCs, including a Ca2+-activated K+ current (IKCa), an inwardly rectifying K+ current (IKir), and a chloride current (ICl). IKir was inhibited by Ba2+, and I KCa was activated by the Ca2+ ionophore A-23187 and inhibited by the intermediate-conductance IKCa channel blocker clotrimazole. ICl was activated by hyposmotic (0.8 T) conditions and inhibited by the chloride channel blockers DIDS and NPPB. The corresponding ion channel genes and proteins, KCa3.1 for IKCa, Kir2.1 for I Kir, and Clcn3 for ICl, were confirmed by RT-PCR and Western immunoblotting analysis in mouse MSCs. These results demonstrate that three types of functional ion channel currents (i.e., IKir, I KCa, and ICl) are present in mouse bone marrow MSCs. Copyright © 2007 the American Physiological Society. |
Persistent Identifier | http://hdl.handle.net/10722/76415 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 1.711 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tao, R | en_HK |
dc.contributor.author | Lau, CP | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.contributor.author | Li, GR | en_HK |
dc.date.accessioned | 2010-09-06T07:20:59Z | - |
dc.date.available | 2010-09-06T07:20:59Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | American Journal Of Physiology - Cell Physiology, 2007, v. 293 n. 5, p. C1561-C1567 | en_HK |
dc.identifier.issn | 0363-6143 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/76415 | - |
dc.description.abstract | Bone marrow mesenchymal stem cells (MSCs) are used as a cell source for cardiomyoplasty; however, the cellular electrophysiological properties are not fully understood. The present study was to investigate the functional ionic channels in undifferentiated mouse bone marrow MSCs using whole cell patch-voltage clamp technique, RT-PCR, and Western immunoblotting analysis. We found that three types of ionic currents were present in mouse MSCs, including a Ca2+-activated K+ current (IKCa), an inwardly rectifying K+ current (IKir), and a chloride current (ICl). IKir was inhibited by Ba2+, and I KCa was activated by the Ca2+ ionophore A-23187 and inhibited by the intermediate-conductance IKCa channel blocker clotrimazole. ICl was activated by hyposmotic (0.8 T) conditions and inhibited by the chloride channel blockers DIDS and NPPB. The corresponding ion channel genes and proteins, KCa3.1 for IKCa, Kir2.1 for I Kir, and Clcn3 for ICl, were confirmed by RT-PCR and Western immunoblotting analysis in mouse MSCs. These results demonstrate that three types of functional ion channel currents (i.e., IKir, I KCa, and ICl) are present in mouse bone marrow MSCs. Copyright © 2007 the American Physiological Society. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpcell.physiology.org/ | en_HK |
dc.relation.ispartof | American Journal of Physiology - Cell Physiology | en_HK |
dc.subject | Intermediate-conductance calcium-activated potassium current | - |
dc.subject | Inward rectifier potassium current | - |
dc.subject | Volume-sensitive chloride current | - |
dc.subject.mesh | 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Barium Compounds - metabolism | en_HK |
dc.subject.mesh | Blotting, Western | en_HK |
dc.subject.mesh | Bone Marrow Cells - drug effects - metabolism | en_HK |
dc.subject.mesh | Calcimycin - pharmacology | en_HK |
dc.subject.mesh | Cell Size | en_HK |
dc.subject.mesh | Cells, Cultured | en_HK |
dc.subject.mesh | Chloride Channels - drug effects - genetics - metabolism | en_HK |
dc.subject.mesh | Chlorides - metabolism | en_HK |
dc.subject.mesh | Clotrimazole - pharmacology | en_HK |
dc.subject.mesh | Intermediate-Conductance Calcium-Activated Potassium Channels - drug effects - genetics - metabolism | en_HK |
dc.subject.mesh | Ionophores - pharmacology | en_HK |
dc.subject.mesh | Membrane Potentials | en_HK |
dc.subject.mesh | Mesenchymal Stem Cells - drug effects - metabolism | en_HK |
dc.subject.mesh | Mice | en_HK |
dc.subject.mesh | Mice, Inbred C57BL | en_HK |
dc.subject.mesh | Nitrobenzoates - pharmacology | en_HK |
dc.subject.mesh | Patch-Clamp Techniques | en_HK |
dc.subject.mesh | Potassium - metabolism | en_HK |
dc.subject.mesh | Potassium Channel Blockers - pharmacology | en_HK |
dc.subject.mesh | Potassium Channels, Inwardly Rectifying - drug effects - genetics - metabolism | en_HK |
dc.subject.mesh | RNA, Messenger - metabolism | en_HK |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_HK |
dc.title | Functional ion channels in mouse bone marrow mesenchymal stem cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0363-6143&volume=293&issue=5&spage=C1561&epage=7&date=2007&atitle=Functional+Ion+Channels+in+Mouse+Bone+Marrow+Mesenchymal+Stem+Cells.+ | 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 | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1152/ajpcell.00240.2007 | en_HK |
dc.identifier.pmid | 17699636 | - |
dc.identifier.scopus | eid_2-s2.0-36049009956 | en_HK |
dc.identifier.hkuros | 139379 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-36049009956&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 293 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | C1561 | en_HK |
dc.identifier.epage | C1567 | en_HK |
dc.identifier.isi | WOS:000250709500015 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Tao, R=7102857104 | en_HK |
dc.identifier.scopusauthorid | Lau, CP=7401968501 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.scopusauthorid | Li, GR=7408462932 | en_HK |
dc.identifier.citeulike | 10063198 | - |
dc.identifier.issnl | 0363-6143 | - |