Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
Cell. 2010 Jul 9;142(1):144-57. doi: 10.1016/j.cell.2010.06.010.
In the mammalian brain, the specification of a single axon and multiple dendrites occurs early in the differentiation of most neuron types. Numerous intracellular signaling events for axon specification have been described in detail. However, the identity of the extracellular factor(s) that initiate neuronal polarity in vivo is unknown. Here, we report that transforming growth factor beta (TGF-beta) initiates signaling pathways both in vivo and in vitro to fate naive neurites into axons. Neocortical neurons lacking the type II TGF-beta receptor (TbetaR2) fail to initiate axons during development. Exogenous TGF-beta is sufficient to direct the rapid growth and differentiation of an axon, and genetic enhancement of receptor activity promotes the formation of multiple axons. Finally, we show that the bulk of these TGF-beta-dependent events are mediated by site-specific phosphorylation of Par6. These results define an extrinsic cue for neuronal polarity in vivo that patterns neural circuits in the developing brain.
在哺乳动物大脑中,大多数神经元类型的分化早期就会特异性地产生单个轴突和多个树突。已经详细描述了许多用于轴突特异性的细胞内信号事件。然而,体内起始神经元极性的细胞外因子(s)的身份尚不清楚。在这里,我们报告转化生长因子β(TGF-β)在体内和体外都启动信号通路,将幼稚神经突命运定型为轴突。缺少 II 型 TGF-β受体(TβR2)的新皮层神经元在发育过程中无法起始轴突。外源性 TGF-β足以指导轴突的快速生长和分化,并且受体活性的遗传增强促进了多个轴突的形成。最后,我们表明,这些 TGF-β 依赖性事件的大部分是通过 Par6 的特定部位磷酸化来介导的。这些结果定义了体内神经元极性的外在线索,为发育中的大脑中的神经回路提供了模式。