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Diversity of Ion Channels in Human Bone Marrow Mesenchymal Stem Cells from Amyotrophic Lateral Sclerosis Patients

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dc.contributor.authorPark, Kyoung Sun-
dc.contributor.authorChoi, Mi Ran-
dc.contributor.authorJung, Kyoung Hwa-
dc.contributor.authorKim, SeungHyun-
dc.contributor.authorKim, Hyun Young-
dc.contributor.authorKim, Kyung Suk-
dc.contributor.authorCha, Eun-Jong-
dc.contributor.authorKim, Yangmi-
dc.contributor.authorChai, Young Gyu-
dc.date.accessioned2022-12-21T00:22:29Z-
dc.date.available2022-12-21T00:22:29Z-
dc.date.issued2008-12-
dc.identifier.issn1226-4512-
dc.identifier.issn2093-3827-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177644-
dc.description.abstractHuman bone marrow mesenchymal stem cells (hBM-MSCs) represent a potentially valuable cell type for clinical therapeutic applications. The present study was designed to evaluate the effect of long-term culturing (up to 10(th) passages) of hBM-MSCs from eight individual amyotrophic lateral sclerosis (ALS) patients, focusing on functional ion channels. All hBM-MSCs contain several MSCs markers with no significant differences, whereas the distribution of functional ion channels was shown to be different between cells. Four types of K+ currents, including noise-like Ca+2-activated K+ current (IKCa), a transient outward K+ current (I-to), a delayed rectifier K+ current (IKDR), and an inward-rectifier K+ current (K;,) were heterogeneously present in these cells, and a TTX-sensitive Na+ current (I-Na,I-TTx) was also recorded. In the RT-PCR analysis, Kv1.1, heag1, Kv4.2, Kir2.1, MaxiK, and hNE-Na were detected. In particular, I-Na,I-TTx showed a significant passage-dependent increase. This is the first report showing that functional ion channel profiling depend on the cellular passage of hBM-MSCs-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisher대한약리학회-
dc.titleDiversity of Ion Channels in Human Bone Marrow Mesenchymal Stem Cells from Amyotrophic Lateral Sclerosis Patients-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4196/kjpp.2008.12.6.337-
dc.identifier.scopusid2-s2.0-58249102257-
dc.identifier.wosid000262525400008-
dc.identifier.bibliographicCitationThe Korean Journal of Physiology & Pharmacology, v.12, no.6, pp 337 - 342-
dc.citation.titleThe Korean Journal of Physiology & Pharmacology-
dc.citation.volume12-
dc.citation.number6-
dc.citation.startPage337-
dc.citation.endPage342-
dc.type.docTypeArticle-
dc.identifier.kciidART001306998-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusCYCLE PROGRESSION-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusTRANSPLANTATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordAuthorBone marrow-
dc.subject.keywordAuthorStem cells-
dc.subject.keywordAuthorFunctional ion channels-
dc.subject.keywordAuthorTetrodotoxin-sensitive Na+ current-
dc.subject.keywordAuthorPassage-dependency-
dc.identifier.urlhttps://synapse.koreamed.org/articles/1025573-
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