Cobalt chloride induces neuronal differentiation of human mesenchymal stem cells through upregulation of microRNA-124a

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• 作者：Eun Su Jeon^a ; ^b ; ¹ ; ² ; Jin Hee Shin^a ; ^b ; ¹ ; Su Jin Hwang^a ; Gyeong Joon Moon^d ; Oh Young Bang^a ; ^c ; Hyeon Ho Kim^a ; ^b ; ^{hyeonhkim@skku.edu" class="auth_mail}
• 关键词：Human mesenchymal stem cells ; Neuronal differentiation ; Cobalt chloride ; Hypoxia-inducible factor-1伪 ; MicroRNA-124a
• 刊名：Biochemical and Biophysical Research Communications
• 出版年：21 February, 2014
• 年：2014
• 卷：444
• 期：4
• 页码：581-587
• 全文大小：1354 K

文摘

Human mesenchymal stem cells (hMSCs) are known to have the capacity to differentiate into various cell types, including neurons. To examine our hypothesis that miRNA was involved in neuronal differentiation of hMSCs, CoCl₂, a hypoxia-mimicking agent was used to induce neuronal differentiation, which was assessed by determining the expression of neuronal markers such as nestin and Tuj1. Treatment of hMSCs with CoCl₂ led to increased expression of miR-124a, a neuron-specific miRNA. HIF-1伪 silencing and JNK inhibition abolished CoCl₂-induced miR-124a expression, suggesting that JNK and HIF-1伪 signals were required for the miR-124a expression induced by CoCl₂ in hMSCs. Overexpression of miR-124a or CoCl₂ treatment suppressed the expression of anti-neural proteins such as SCP1 and SOX9. Silencing of both SCP1 and SOX9 induced neuronal differentiation of hMSCs, indicating that suppression of miR-124a targets is important for CoCl₂-induced neuronal differentiation of hMSCs. Knockdown of HIF-1伪 or inhibition of JNK restored the expression of SCP1 and SOX9 in CoCl₂-treated cells. Inhibition of miR-124a blocked CoCl₂-induced suppression of SCP1 and SOX9 and abolished CoCl₂-induced neuronal differentiation of hMSCs. Taken together, we demonstrate that miR-124a is critically regulates CoCl₂-induced neuronal differentiation of hMSCs by suppressing the expression of SCP1 and SOX9.