Department of Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI 48824, USA.
Cell Mol Life Sci. 2011 Mar;68(5):863-76. doi: 10.1007/s00018-010-0497-1. Epub 2010 Aug 20.
The intracellular second messenger cAMP is frequently used in induction media to induce mesenchymal stem cells (MSCs) into neural lineage cells. To date, an understanding of the role cAMP exerts on MSCs and whether cAMP can induce MSCs into functional neurons is still lacking. We found cAMP initiated neuron-like morphology changes early and neural differentiation much later. The early phase changes in morphology were due to cell shrinkage, which subsequently rendered some cells apoptotic. While the morphology changes occurred prior to the expression of neural markers, it is not required for neural marker expression and the two processes are differentially regulated downstream of cAMP-activated protein kinase A. cAMP enabled MSCs to gain neural marker expressions with neuronal function, such as, calcium rise in response to neuronal activators, dopamine, glutamate, and potassium chloride. However, only some of the cells induced by cAMP responded to the three neuronal activators and further lack the neuronal morphology, suggesting that although cAMP is able to direct MSCs towards neural differentiation, they do not achieve terminal differentiation.
细胞内第二信使 cAMP 常用于诱导培养基中,将间充质干细胞 (MSCs) 诱导为神经谱系细胞。迄今为止,人们对 cAMP 对 MSCs 的作用以及 cAMP 是否能诱导 MSCs 成为功能性神经元仍知之甚少。我们发现 cAMP 早期引发神经元样形态变化,随后才引发神经分化。形态早期的变化是由于细胞收缩,随后导致一些细胞凋亡。虽然形态变化发生在神经标志物表达之前,但这不是神经标志物表达所必需的,这两个过程在 cAMP 激活蛋白激酶 A 的下游受到不同的调节。cAMP 使 MSCs 获得具有神经元功能的神经标志物表达,例如,神经元激活剂、多巴胺、谷氨酸和氯化钾引起的钙上升。然而,只有部分由 cAMP 诱导的细胞对三种神经元激活剂有反应,并且进一步缺乏神经元形态,这表明尽管 cAMP 能够指导 MSCs 向神经分化,但它们不能实现终末分化。