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

Authors
Park, Kyoung SunChoi, Mi RanJung, Kyoung HwaKim, SeungHyunKim, Hyun YoungKim, Kyung SukCha, Eun-JongKim, YangmiChai, Young Gyu
Issue Date
Dec-2008
Publisher
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
Keywords
Bone marrow; Stem cells; Functional ion channels; Tetrodotoxin-sensitive Na+ current; Passage-dependency
Citation
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.12, no.6, pp.337 - 342
Indexed
SCIE
SCOPUS
KCI
Journal Title
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
Volume
12
Number
6
Start Page
337
End Page
342
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177644
DOI
10.4196/kjpp.2008.12.6.337
ISSN
1226-4512
Abstract
Human 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
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