Pacary Emilie, Tixier Emmanuelle, Coulet Florence, Roussel Simon, Petit Edwige, Bernaudin Myriam
UMR-CNRS 6185, Hypoxia and Cerebrovascular Physiopathology Group, University of Caen, CYCERON, Bd Henri Becquerel, BP 5229, F-14074 Caen cedex, France.
Mol Cell Neurosci. 2007 Jul;35(3):409-23. doi: 10.1016/j.mcn.2007.04.002. Epub 2007 Apr 10.
This study demonstrates that the Rho-kinase (ROCK) inhibitor, Y-27632, potentiates not only the effect of cobalt chloride (CoCl(2)) but also that of deferoxamine, another HIF-1 inducer, on mesenchymal stem cell (MSC) neuronal differentiation. HIF-1 is essential for CoCl(2)+/-Y-27632-induced MSC neuronal differentiation, since agents inhibiting HIF-1 abolish the changes of morphology and cell cycle arrest-related gene or protein expressions (p21, cyclin D1) and the increase of neuronal marker expressions (Tuj1, NSE). Y-27632 potentiates the CoCl(2)-induced decrease of cyclin D1 and nestin expressions, the increase of HIF-1 activation and EPO expression, and decreases pVHL expression. Interestingly, CoCl(2) decreases RhoA expression, an effect potentiated by Y-27632, revealing crosstalk between HIF-1 and RhoA/ROCK pathways. Moreover, we demonstrate a synergistic effect of CoCl(2) and Y-27632 on neurosphere differentiation into neurons and PC12 neurite outgrowth underlining that a co-treatment targeting both HIF-1 and ROCK pathways might be relevant to differentiate stem cells into neurons.
本研究表明,Rho激酶(ROCK)抑制剂Y-27632不仅能增强氯化钴(CoCl₂)对间充质干细胞(MSC)向神经元分化的作用,还能增强另一种低氧诱导因子-1(HIF-1)诱导剂去铁胺的作用。HIF-1对于CoCl₂+/-Y-27632诱导的MSC向神经元分化至关重要,因为抑制HIF-1的试剂会消除形态学变化以及细胞周期阻滞相关基因或蛋白表达(p21、细胞周期蛋白D1)的改变,以及神经元标志物表达(Tuj1、神经元特异性烯醇化酶)的增加。Y-27632增强了CoCl₂诱导的细胞周期蛋白D1和巢蛋白表达的降低、HIF-1激活和促红细胞生成素表达的增加,并降低了pVHL表达。有趣的是,CoCl₂降低了RhoA表达,Y-27632增强了这一作用,揭示了HIF-1与RhoA/ROCK通路之间的相互作用。此外,我们证明了CoCl₂和Y-27632在神经球向神经元分化以及PC12神经突生长方面具有协同作用,强调针对HIF-1和ROCK通路的联合治疗可能与将干细胞分化为神经元相关。