Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2010 Apr 15;24(8):799-813. doi: 10.1101/gad.1880510.
Neuronal polarity is essential for normal brain development and function. However, cell-intrinsic mechanisms that govern the establishment of neuronal polarity remain to be identified. Here, we report that knockdown of endogenous FOXO proteins in hippocampal and cerebellar granule neurons, including in the rat cerebellar cortex in vivo, reveals a requirement for the FOXO transcription factors in the establishment of neuronal polarity. The FOXO transcription factors, including the brain-enriched protein FOXO6, play a critical role in axo-dendritic polarization of undifferentiated neurites, and hence in a switch from unpolarized to polarized neuronal morphology. We also identify the gene encoding the protein kinase Pak1, which acts locally in neuronal processes to induce polarity, as a critical direct target gene of the FOXO transcription factors. Knockdown of endogenous Pak1 phenocopies the effect of FOXO knockdown on neuronal polarity. Importantly, exogenous expression of Pak1 in the background of FOXO knockdown in both primary neurons and postnatal rat pups in vivo restores the polarized morphology of neurons. These findings define the FOXO proteins and Pak1 as components of a cell-intrinsic transcriptional pathway that orchestrates neuronal polarity, thus identifying a novel function for the FOXO transcription factors in a unique aspect of neural development.
神经元极性对于正常的大脑发育和功能至关重要。然而,支配神经元极性建立的细胞内机制仍有待确定。在这里,我们报告说,在海马和小脑颗粒神经元中敲低内源性 FOXO 蛋白,包括在体内大鼠小脑皮质中,揭示了 FOXO 转录因子在建立神经元极性中的必要性。FOXO 转录因子,包括富含大脑的 FOXO6 蛋白,在未分化神经突的轴突-树突极性形成中发挥关键作用,从而在非极化到极化神经元形态的转变中发挥关键作用。我们还确定了编码蛋白激酶 Pak1 的基因,该基因在神经元过程中局部作用诱导极性,是 FOXO 转录因子的一个关键直接靶基因。内源性 Pak1 的敲低模拟了 FOXO 敲低对神经元极性的影响。重要的是,FOXO 敲低背景下外源表达 Pak1 在体内原代神经元和新生大鼠幼仔中恢复神经元的极化形态。这些发现将 FOXO 蛋白和 Pak1 定义为协调神经元极性的细胞内转录途径的组成部分,从而确定了 FOXO 转录因子在神经发育独特方面的新功能。