Frost Emma E, Zhou Zhicheng, Krasnesky Kimberley, Armstrong Regina C
Department of Pathology, University of Manitoba, JBRC401, 727 McDermot Avenue, Winnipeg, MB, Canada, R3E 3P5.
Neurochem Res. 2009 Jan;34(1):169-81. doi: 10.1007/s11064-008-9748-z. Epub 2008 May 30.
During CNS development, oligodendrocyte progenitor (OP) cells migrate from germinal zones to presumptive white matter tracts to generate myelinating oligodendrocytes. In vitro and in vivo studies indicate that platelet-derived growth factor-A (PDGF-A) is a potent chemoattractant for OP cells and important for normal distribution throughout the developing CNS. However, PDGF-A does not localize in concentration gradients corresponding to OP migratory pathways, as would be expected for a chemoattractant to direct migration. Therefore, the mechanism by which PDGF-A regulates OP distribution remains to be clarified. Here we show that PDGF-A induces OP migration and continuous exposure to PDGF-A is not required to maintain migration. Using pharmacological inhibitors, we show that a self-sustaining extracellular-regulated-kinase signaling pathway drives OP migration for up to 72 hours after the initial PDGF stimulus. These findings indicate PDGF-A may act to mobilize OP cells that then respond to distinct directional signals to distribute appropriately within the CNS.
在中枢神经系统(CNS)发育过程中,少突胶质前体细胞(OP)从生发区迁移至假定的白质束,以生成髓鞘形成少突胶质细胞。体外和体内研究表明,血小板衍生生长因子-A(PDGF-A)是OP细胞的一种有效趋化因子,对其在整个发育中的中枢神经系统的正常分布很重要。然而,PDGF-A并不像预期的趋化因子引导迁移那样,以与OP迁移途径相对应的浓度梯度定位。因此,PDGF-A调节OP分布的机制仍有待阐明。在这里,我们表明PDGF-A诱导OP迁移,并且维持迁移不需要持续暴露于PDGF-A。使用药理学抑制剂,我们表明,在最初的PDGF刺激后,一种自我维持的细胞外调节激酶信号通路驱动OP迁移长达72小时。这些发现表明,PDGF-A可能起到动员OP细胞的作用,然后这些细胞对不同的定向信号作出反应,以在中枢神经系统内适当分布。