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- Publisher Website: 10.1634/stemcells.2004-0213
- Scopus: eid_2-s2.0-15544379480
- PMID: 15749932
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Article: Characterization of ionic currents in human mesenchymal stem cells from bone marrow
Title | Characterization of ionic currents in human mesenchymal stem cells from bone marrow |
---|---|
Authors | |
Keywords | Ca2+-activated K+ current Heag K+ current Human mesenchymal stem cells Ion channels Transient outward K+ current TTX-sensitive Na+ current |
Issue Date | 2005 |
Publisher | AlphaMed Press, Inc. The Journal's web site is located at http://www.stemcells.com |
Citation | Stem Cells, 2005, v. 23 n. 3, p. 371-382 How to Cite? |
Abstract | This study characterized functional ion channels in cultured undifferentiated human mesenchymal stem cells (hMSCs) from bone marrow with whole-cell patch clamp and reverse transcription polymerase chain reaction (RT-PCR) techniques. Three types of outward currents were found in hMSCs, including a noise-like rapidly activating outward current inhibited by the large conductance Ca2+-activated K+ channel (IKCa) blocker iberiotoxin, a transient outward K+ current (Ito) suppressed by 4-aminopyridine (4-AP), and a delayed rectifier K+ current (IKDR)-like ether-à-go-go (eag) K+ channel. In addition, tetrodotoxin-sensitive sodium current (INa.TTX) and nifedipine-sensitive L-type Ca2+ current (ICa.L) were also detected in 29% and 15% hMSCs, respectively. Moreover, RT-PCR revealed the molecular evidence of high levels of mRNA for the functional ionic currents, including human MaxiK for IKCa, Kv4.2 and Kv1.4 for Ito, heag1 for IKDR, hNE-Na for INa.TTX, and CACNAIC for I Ca.L. These results demonstrate that multiple functional ion channel currents-that is, IKca, Ito heag1, INa.TTX, and ICa.L-are expressed in hMSCs from bone marrow. |
Persistent Identifier | http://hdl.handle.net/10722/85513 |
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.396 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, GR | en_HK |
dc.contributor.author | Sun, H | en_HK |
dc.contributor.author | Deng, X | en_HK |
dc.contributor.author | Lau, CP | en_HK |
dc.date.accessioned | 2010-09-06T09:05:57Z | - |
dc.date.available | 2010-09-06T09:05:57Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Stem Cells, 2005, v. 23 n. 3, p. 371-382 | en_HK |
dc.identifier.issn | 1066-5099 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/85513 | - |
dc.description.abstract | This study characterized functional ion channels in cultured undifferentiated human mesenchymal stem cells (hMSCs) from bone marrow with whole-cell patch clamp and reverse transcription polymerase chain reaction (RT-PCR) techniques. Three types of outward currents were found in hMSCs, including a noise-like rapidly activating outward current inhibited by the large conductance Ca2+-activated K+ channel (IKCa) blocker iberiotoxin, a transient outward K+ current (Ito) suppressed by 4-aminopyridine (4-AP), and a delayed rectifier K+ current (IKDR)-like ether-à-go-go (eag) K+ channel. In addition, tetrodotoxin-sensitive sodium current (INa.TTX) and nifedipine-sensitive L-type Ca2+ current (ICa.L) were also detected in 29% and 15% hMSCs, respectively. Moreover, RT-PCR revealed the molecular evidence of high levels of mRNA for the functional ionic currents, including human MaxiK for IKCa, Kv4.2 and Kv1.4 for Ito, heag1 for IKDR, hNE-Na for INa.TTX, and CACNAIC for I Ca.L. These results demonstrate that multiple functional ion channel currents-that is, IKca, Ito heag1, INa.TTX, and ICa.L-are expressed in hMSCs from bone marrow. | en_HK |
dc.language | eng | en_HK |
dc.publisher | AlphaMed Press, Inc. The Journal's web site is located at http://www.stemcells.com | en_HK |
dc.relation.ispartof | Stem Cells | en_HK |
dc.subject | Ca2+-activated K+ current | - |
dc.subject | Heag K+ current | - |
dc.subject | Human mesenchymal stem cells | - |
dc.subject | Ion channels | - |
dc.subject | Transient outward K+ current | - |
dc.subject | TTX-sensitive Na+ current | - |
dc.subject.mesh | 4-Aminopyridine - pharmacology | en_HK |
dc.subject.mesh | Bone Marrow Cells - cytology - drug effects - physiology | en_HK |
dc.subject.mesh | Calcium Channels, L-Type - drug effects - genetics - physiology | en_HK |
dc.subject.mesh | Cell Differentiation | en_HK |
dc.subject.mesh | Cells, Cultured | en_HK |
dc.subject.mesh | Ether-A-Go-Go Potassium Channels | en_HK |
dc.subject.mesh | Gene Expression - genetics | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Ion Channels - genetics - physiology | en_HK |
dc.subject.mesh | Kv1.4 Potassium Channel | en_HK |
dc.subject.mesh | Large-Conductance Calcium-Activated Potassium Channel alpha Subunits | en_HK |
dc.subject.mesh | Large-Conductance Calcium-Activated Potassium Channels | en_HK |
dc.subject.mesh | Membrane Potentials - drug effects | en_HK |
dc.subject.mesh | Mesenchymal Stem Cells - cytology - drug effects - physiology | en_HK |
dc.subject.mesh | Nerve Tissue Proteins - genetics | en_HK |
dc.subject.mesh | Nifedipine - pharmacology | en_HK |
dc.subject.mesh | Patch-Clamp Techniques | en_HK |
dc.subject.mesh | Peptides - pharmacology | en_HK |
dc.subject.mesh | Potassium Channels - genetics | en_HK |
dc.subject.mesh | Potassium Channels, Calcium-Activated - drug effects - genetics - physiology | en_HK |
dc.subject.mesh | Potassium Channels, Voltage-Gated - drug effects - genetics - physiology | en_HK |
dc.subject.mesh | RNA, Messenger - genetics - metabolism | en_HK |
dc.subject.mesh | Shal Potassium Channels | en_HK |
dc.subject.mesh | Sodium Channels - drug effects - genetics - physiology | en_HK |
dc.subject.mesh | Tetrodotoxin - pharmacology | en_HK |
dc.title | Characterization of ionic currents in human mesenchymal stem cells from bone marrow | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1066-5099&volume=23&issue=3&spage=371&epage=382&date=2005&atitle=Characterization+of+ionic+currents+in+human+mesenchymal+stem+cells+from+bone+marrow | en_HK |
dc.identifier.email | Li, GR:grli@hkucc.hku.hk | en_HK |
dc.identifier.authority | Li, GR=rp00476 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1634/stemcells.2004-0213 | en_HK |
dc.identifier.pmid | 15749932 | - |
dc.identifier.scopus | eid_2-s2.0-15544379480 | en_HK |
dc.identifier.hkuros | 101185 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-15544379480&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 23 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 371 | en_HK |
dc.identifier.epage | 382 | en_HK |
dc.identifier.isi | WOS:000227786900010 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Li, GR=7408462932 | en_HK |
dc.identifier.scopusauthorid | Sun, H=35723049200 | en_HK |
dc.identifier.scopusauthorid | Deng, X=14057894600 | en_HK |
dc.identifier.scopusauthorid | Lau, CP=7401968501 | en_HK |
dc.identifier.issnl | 1066-5099 | - |