Kong Sun-Young, Park Min-Hye, Lee Mina, Kim Jae-Ouk, Lee Ha-Rim, Han Byung Woo, Svendsen Clive N, Sung Sang Hyun, Kim Hyun-Jung
Laboratory of Molecular and Stem Cell Pharmacology, College of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
College of Pharmacy and Research Institute of Pharmaceutical Science, Seoul National University, Seoul, Republic of Korea; College of Pharmacy, Sunchon National University, Suncheon, Jeollanam-do, Republic of Korea.
PLoS One. 2015 Feb 23;10(2):e0118188. doi: 10.1371/journal.pone.0118188. eCollection 2015.
Neural stem cells (NSCs) have the ability to proliferate and differentiate into neurons and glia. Regulation of NSC fate by small molecules is important for the generation of a certain type of cell. The identification of small molecules that can induce new neurons from NSCs could facilitate regenerative medicine and drug development for neurodegenerative diseases. In this study, we screened natural compounds to identify molecules that are effective on NSC cell fate determination. We found that Kuwanon V (KWV), which was isolated from the mulberry tree (Morus bombycis) root, increased neurogenesis in rat NSCs. In addition, during NSC differentiation, KWV increased cell survival and inhibited cell proliferation as shown by 5-bromo-2-deoxyuridine pulse experiments, Ki67 immunostaining and neurosphere forming assays. Interestingly, KWV enhanced neuronal differentiation and decreased NSC proliferation even in the presence of mitogens such as epidermal growth factor and fibroblast growth factor 2. KWV treatment of NSCs reduced the phosphorylation of extracellular signal-regulated kinase 1/2, increased mRNA expression levels of the cyclin-dependent kinase inhibitor p21, down-regulated Notch/Hairy expression levels and up-regulated microRNA miR-9, miR-29a and miR-181a. Taken together, our data suggest that KWV modulates NSC fate to induce neurogenesis, and it may be considered as a new drug candidate that can regenerate or protect neurons in neurodegenerative diseases.
神经干细胞(NSCs)具有增殖并分化为神经元和神经胶质细胞的能力。小分子对神经干细胞命运的调控对于特定类型细胞的生成至关重要。鉴定能够从神经干细胞诱导产生新神经元的小分子,有助于再生医学和神经退行性疾病的药物研发。在本研究中,我们筛选了天然化合物以鉴定对神经干细胞命运决定有效的分子。我们发现,从桑树(桑)根中分离出的桑酮V(KWV)可增加大鼠神经干细胞中的神经发生。此外,在神经干细胞分化过程中,5-溴-2-脱氧尿苷脉冲实验、Ki67免疫染色和神经球形成试验表明,KWV可提高细胞存活率并抑制细胞增殖。有趣的是,即使在存在表皮生长因子和成纤维细胞生长因子2等有丝分裂原的情况下,KWV也能增强神经元分化并减少神经干细胞增殖。用KWV处理神经干细胞可降低细胞外信号调节激酶1/2的磷酸化水平,增加细胞周期蛋白依赖性激酶抑制剂p21的mRNA表达水平,下调Notch/Hairy表达水平并上调微小RNA miR-9、miR-29a和miR-181a。综上所述,我们的数据表明KWV可调节神经干细胞命运以诱导神经发生,它可能被视为一种可在神经退行性疾病中使神经元再生或保护神经元的新候选药物。
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