Department of Biology, College of Natural Sciences, Chosun University, GwangJu 501-759, Republic of Korea.
Neurosci Lett. 2013 Oct 25;554:22-7. doi: 10.1016/j.neulet.2013.08.059. Epub 2013 Sep 8.
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.
最近的研究表明,组蛋白去乙酰化酶(HDACs)的抑制诱导了不同癌症和干细胞的分化,这表明 HDAC 抑制剂可能是诱导干细胞分化的良好候选物。在这项研究中,我们研究了组蛋白去乙酰化酶抑制剂丙戊酸(VPA)对人骨髓间充质基质细胞(hBM-MSCs)向神经元分化的影响。通过实时 PCR 和免疫印迹分析,发现 VPA 处理的 MSC 其神经祖细胞标志物巢蛋白、Musashi、CD133 和 GFAP 的表达显著增加。当 VPA 预处理的 MSC 用神经元诱导培养基(VPA-dMSCs)分化时,它们表现出与神经元相似的细胞体和树突形态。与分化的 MSC(dMSCs)相比,这些 VPA-dMSCs 的数量和神经突长度显著增加。VPA-dMSCs 和 dMSCs 的神经元特异性标记基因,包括 Nestin、Musashi、CD133、GFAP、NeuN、MAP-2、NF-M、KCNH1 和 KCNH5 的转录水平显著增加。通过免疫细胞化学染色和免疫印迹分析,这些细胞还显示出神经元标记蛋白 Nestin 和 NF-M 的更高表达。这项研究表明,VPA 预处理 hBM-MSCs 后,用神经元诱导培养基孵育,可有效刺激 BM-MSCs 向神经元细胞分化。