Kwiatkowski Adam V, Rubinson Douglas A, Dent Erik W, Edward van Veen J, Leslie Jonathan D, Zhang Jiangyang, Mebane Leslie M, Philippar Ulrike, Pinheiro Elaine M, Burds Aurora A, Bronson Roderick T, Mori Susumu, Fässler Reinhard, Gertler Frank B
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Neuron. 2007 Nov 8;56(3):441-55. doi: 10.1016/j.neuron.2007.09.008.
Mammalian cortical development involves neuronal migration and neuritogenesis; this latter process forms the structural precursors to axons and dendrites. Elucidating the pathways that regulate the cytoskeleton to drive these processes is fundamental to our understanding of cortical development. Here we show that loss of all three murine Ena/VASP proteins, a family of actin regulatory proteins, causes neuronal ectopias, alters intralayer positioning in the cortical plate, and, surprisingly, blocks axon fiber tract formation during corticogenesis. Cortical fiber tract defects in the absence of Ena/VASP arise from a failure in neurite initiation, a prerequisite for axon formation. Neurite initiation defects in Ena/VASP-deficient neurons are preceded by a failure to form bundled actin filaments and filopodia. These findings provide insight into the regulation of neurite formation and the role of the actin cytoskeleton during cortical development.
哺乳动物的皮质发育涉及神经元迁移和神经突形成;后一过程形成轴突和树突的结构前体。阐明调节细胞骨架以驱动这些过程的途径对于我们理解皮质发育至关重要。在这里,我们表明,三种小鼠Ena/VASP蛋白(一类肌动蛋白调节蛋白)的缺失会导致神经元异位,改变皮质板内的层内定位,并且令人惊讶的是,在皮质发生过程中会阻止轴突纤维束的形成。在没有Ena/VASP的情况下,皮质纤维束缺陷源于神经突起始的失败,而神经突起始是轴突形成的先决条件。Ena/VASP缺陷神经元的神经突起始缺陷之前是未能形成成束的肌动蛋白丝和丝状伪足。这些发现为皮质发育过程中神经突形成的调节以及肌动蛋白细胞骨架的作用提供了见解。