Children's Nutrition Research Center, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.
Int J Biochem Cell Biol. 2013 Apr;45(4):866-75. doi: 10.1016/j.biocel.2013.01.002. Epub 2013 Jan 11.
All-trans retinoic acid plays an important role in nervous system development. However, the effects of all-trans retinoic acid on the neuronal differentiation of mesenchymal stem cells and the mechanisms through which this differentiation takes place are still poorly understood. Here, we investigated the biological effects of all-trans retinoic acid on the neuronal differentiation of mesenchymal stem cells and the signaling pathways that mediated these effects. We found that the neuronal differentiation efficiency of mesenchymal stem cells following all-trans retinoic acid pre-induction was greater and the axonal length was longer than was observed with mesenchymal stem cells that were not pre-induced. mRNA and protein levels of the neural-markers Nestin, NSE, MAP-2, Tau and Tuj1 were stronger in neural-like cells derived from all-trans retinoic acid-pretreated mesenchymal stem cells than in those not pre-induction. Interestingly, the neuronal excitability of differentiated neural-like cells exhibited the same patterns between these two groups. Clear expression of retinoic acid receptor alpha and gamma in mesenchymal stem cells was observed, while retinoic acid receptor beta was barely detected. However, retinoic acid receptor beta expression in mesenchymal stem cells after neuronal induction increased dramatically, in contrast with retinoic acid receptor alpha and gamma expression, and retinoic acid receptor beta expression in mesenchymal stem cells receiving all-trans retinoic acid pre-induction was even stronger. Next, retinoic acid receptor alpha, beta and gamma were over-expressed by recombinant adenovirus infection prior to neuronal induction. Retinoic acid receptor alpha and gamma over-expression did not impact the neuronal differentiation of mesenchymal stem cells. However, retinoic acid receptor beta over-expression promoted neuronal differentiation to a similar level as observed following all-trans retinoic acid pre-induction. The neuronal differentiation promoting effects of all-trans retinoic acid on mesenchymal stem cells could be inhibited by siRNA silencing of retinoic acid receptor beta and by LE135, an inhibitor of retinoic acid receptor beta. Taken together, these results suggest that all-trans retinoic acid pre-induction facilitates the neuronal differentiation of mesenchymal stem cells. These facilitation effects are achieved by activating the retinoic acid receptor beta signaling pathway.
全反式视黄酸在神经系统发育中起着重要作用。然而,全反式视黄酸对间充质干细胞的神经元分化的影响及其发生的机制仍知之甚少。在这里,我们研究了全反式视黄酸对间充质干细胞的神经元分化的生物学影响以及介导这些影响的信号通路。我们发现,与未经预诱导的间充质干细胞相比,经全反式视黄酸预诱导后的间充质干细胞的神经元分化效率更高,轴突更长。神经样细胞中神经标志物巢蛋白、NSE、MAP-2、Tau 和 Tuj1 的 mRNA 和蛋白水平在经全反式视黄酸预处理的间充质干细胞中比未经预诱导的间充质干细胞更强。有趣的是,这两组间分化后的神经样细胞的神经元兴奋性表现出相同的模式。在间充质干细胞中清晰地表达了视黄酸受体 alpha 和 gamma,而几乎检测不到视黄酸受体 beta。然而,在神经诱导后,间充质干细胞中的视黄酸受体 beta 表达显著增加,与视黄酸受体 alpha 和 gamma 表达相反,并且接受全反式视黄酸预诱导的间充质干细胞中的视黄酸受体 beta 表达甚至更强。接下来,在进行神经元诱导之前,通过重组腺病毒感染过表达视黄酸受体 alpha、beta 和 gamma。视黄酸受体 alpha 和 gamma 的过表达对视黄酸受体 beta 的过表达不影响间充质干细胞的神经元分化。然而,视黄酸受体 beta 的过表达促进神经元分化至与全反式视黄酸预诱导相似的水平。全反式视黄酸对间充质干细胞的神经元分化促进作用可以通过视黄酸受体 beta 的 siRNA 沉默和视黄酸受体 beta 的抑制剂 LE135 抑制。综上所述,这些结果表明全反式视黄酸预诱导促进间充质干细胞的神经元分化。这些促进作用是通过激活视黄酸受体 beta 信号通路实现的。