Hu J-G, Fu S-L, Wang Y-X, Li Y, Jiang X-Y, Wang X-F, Qiu M-S, Lu P-H, Xu X-M
Department of Neurobiology, Shanghai Jiaotong University School of Medicine, Shanghai 200025, People's Republic of China.
Neuroscience. 2008 Jan 2;151(1):138-47. doi: 10.1016/j.neuroscience.2007.10.050. Epub 2007 Nov 17.
Platelet-derived growth factor-AA (PDGF-AA) has been used as a potent mitogen for the proliferation of oligodendrocyte progenitor cells (OPCs). Whether it plays a role in oligodendrocyte lineage differentiation of neural stem cells (NSCs) is unclear. Here we report that PDGF-AA is an instructional signal required for the differentiation of embryonic forebrain NSCs into O4-positive oligodendrocytes. Moreover, such PDGF-AA-induced oligodendrocyte differentiation appears to be mediated by the extracellular signal-regulated kinases 1 and 2 (Erk1/2) but not phosphatidylinositol-3 kinase (PI3K) pathway. Finally, PDGF-AA treatment resulted in a significant increase in the expression of the oligodendrocyte-specific transcriptional factor Olig2 in an Erk1/2-dependent mechanism at early stages of oligodendrogliogenesis. Together, our studies provide cellular and molecular evidence to suggest that PDGF-AA is a key molecule that regulates the differentiation of embryonic NSCs into oligodendrocytes. The action of PDGF-AA is mediated by the activation of Erk pathway which involves the downstream upregulation of transcriptional factor Olig2.
血小板衍生生长因子-AA(PDGF-AA)已被用作少突胶质前体细胞(OPC)增殖的强效有丝分裂原。它是否在神经干细胞(NSC)的少突胶质细胞系分化中发挥作用尚不清楚。在此我们报告,PDGF-AA是胚胎前脑NSC分化为O4阳性少突胶质细胞所需的指导性信号。此外,这种由PDGF-AA诱导的少突胶质细胞分化似乎是由细胞外信号调节激酶1和2(Erk1/2)介导的,而非磷脂酰肌醇-3激酶(PI3K)途径。最后,在少突胶质细胞生成早期,PDGF-AA处理通过一种依赖Erk1/2的机制导致少突胶质细胞特异性转录因子Olig2的表达显著增加。总之,我们的研究提供了细胞和分子证据,表明PDGF-AA是调节胚胎NSC向少突胶质细胞分化的关键分子。PDGF-AA的作用是通过激活Erk途径介导的,这涉及转录因子Olig2的下游上调。