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Valproic acid promotes neuronal differentiation by induction of neuroprogenitors in human bone-marrow mesenchymal stromal cells

Authors
Jeong, Sin-GuOhn, TakbumKim, Seung HyunCho, Goang-Won
Issue Date
Oct-2013
Publisher
Elsevier BV
Keywords
Bone marrow-mesenchymal stem cells (BM-MSCs); Mesenchymal stem cells (MSCs); Valproic acid (VPA); Neuronal differentiation; Histone deacetylase (HDAC)
Citation
Neuroscience Letters, v.554, pp 22 - 27
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
Neuroscience Letters
Volume
554
Start Page
22
End Page
27
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/161873
DOI
10.1016/j.neulet.2013.08.059
ISSN
0304-3940
1872-7972
Abstract
Recent studies have shown that the inhibition of histone deacetylases (HDACs) induces the differentiation of diverse cancer and stem cells, which suggests HDAC inhibitors may be good candidates for the induction of stem cell differentiation. In this study, we investigated the effects of a HDAC inhibitor, valproic acid (VPA), for the neuronal differentiation of human bone marrow-mesenchymal stromal cells (hBM- MSCs). VPA-treated MSCs had significant increases in their expression of the neuro-progenitor marker Nestin, Musashi, CD133, and GFAP, as measured by real-time PCR and immunoblot analysis. When VPA-pretreated MSCs were differentiated with neuronal induction media (VPA-dMSCs), they exhibited a cell body and dendritic morphology similar to neurons. The number and neurite length of these VPA-dMSCs significantly increased compared to differentiated MSCs (dMSCs). The VPA-dMSCs and dMSCs had significantly increased transcripts of neuronal-specific marker genes, including Nestin, Musashi, CD133, GFAP, NeuN, MAP-2, NF-M, KCNH1, and KCNH5. The cells also showed a higher expression of the neuronal marker proteins Nestin and NF-M from immunocytochemical staining and immunoblot analysis. This study has shown that VPA pretreatment of hBM-MSCs, following their incubation with neuronal induction media, effectively stimulates neuronal cell differentiation to BM-MSCs.
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