Department of Biophysics, Kyoto University Graduate School of Science, Sakyo-ku, Kyoto, Japan.
Eur J Neurosci. 2010 Feb;31(3):410-24. doi: 10.1111/j.1460-9568.2009.07070.x. Epub 2010 Jan 25.
Callosal projection neurons, one of the major types of projection neurons in the mammalian cerebral cortex, require neuronal activity for their axonal projections [H. Mizuno et al. (2007) J. Neurosci., 27, 6760-6770; C. L. Wang et al. (2007) J. Neurosci., 27, 11334-11342]. Here we established a method to label a few callosal axons with enhanced green fluorescent protein in the mouse cerebral cortex and examined the effect of pre-synaptic/post-synaptic neuron silencing on the morphology of individual callosal axons. Pre-synaptic/post-synaptic neurons were electrically silenced by Kir2.1 potassium channel overexpression. Single axon tracing showed that, after reaching the cortical innervation area, green fluorescent protein-labeled callosal axons underwent successive developmental stages: axon growth, branching, layer-specific targeting and arbor formation between post-natal day (P)5 and P9, and the subsequent elaboration of axon arbors between P9 and P15. Reducing pre-synaptic neuronal activity disturbed axon growth and branching before P9, as well as arbor elaboration afterwards. In contrast, silencing post-synaptic neurons disturbed axon arbor elaboration between P9 and P15. Thus, pre-synaptic neuron silencing affected significantly earlier stages of callosal projection neuron axon development than post-synaptic neuron silencing. Silencing both pre-synaptic and post-synaptic neurons impaired callosal axon projections, suggesting that certain levels of firing activity in pre-synaptic and post-synaptic neurons are required for callosal axon development. Our findings provide in-vivo evidence that pre-synaptic and post-synaptic neuronal activities play critical, and presumably differential, roles in axon growth, branching, arbor formation and elaboration during cortical axon development.
连合投射神经元是哺乳动物大脑皮层主要的投射神经元之一,其轴突投射需要神经元活动[H. Mizuno 等人(2007),《神经科学杂志》,27,6760-6770;C. L. Wang 等人(2007),《神经科学杂志》,27,11334-11342]。在这里,我们建立了一种在小鼠大脑皮层中标记少量连合轴突的方法,并研究了突触前/后神经元沉默对单个连合轴突形态的影响。通过过表达 Kir2.1 钾通道来沉默突触前/后神经元。单轴突追踪显示,在到达皮质投射区后,绿色荧光蛋白标记的连合轴突经历了连续的发育阶段:轴突生长、分支、层特异性靶向和树突形成,发生在出生后第 5 天(P)到第 9 天之间,随后在第 9 天到第 15 天之间进行轴突树突的精细化。减少突触前神经元的活动会干扰 P9 之前的轴突生长和分支,以及之后的树突形成。相比之下,沉默突触后神经元会干扰 P9 到 P15 之间的轴突树突形成。因此,突触前神经元沉默比突触后神经元沉默更早地影响连合投射神经元轴突发育的早期阶段。沉默突触前和后神经元会损害连合轴突投射,这表明突触前和后神经元的一定水平的放电活动对于连合轴突发育是必需的。我们的研究结果提供了体内证据,表明突触前和后神经元的活动在皮质轴突发育过程中对于轴突生长、分支、树突形成和精细化具有关键的、可能不同的作用。