Uesaka Naofumi, Hayano Yasufumi, Yamada Akito, Yamamoto Nobuhiko
Neuroscience Laboratories, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan.
J Neurosci. 2007 May 9;27(19):5215-23. doi: 10.1523/JNEUROSCI.4685-06.2007.
Target and activity-dependent mechanisms of axonal branching were studied in the thalamocortical (TC) projection using organotypic cocultures of the thalamus and cortex. TC axons were labeled with enhanced yellow fluorescent protein (EYFP) by a single-cell electroporation method and observed over time by confocal microscopy. Changes in the firing activity of cocultures grown on multielectrode dishes were also monitored over time. EYFP-labeled TC axons exhibited more branch formation in and around layer 4 of the cortical explant during the second week in vitro, when spontaneous firing activity increased in both thalamic and cortical cells. Time-lapse imaging further demonstrated that branching patterns were generated dynamically by addition and elimination with a bias toward branch accumulation in the target layer. To examine the relationship between neural activity and TC branch formation, the dynamics of axonal branching was analyzed under various pharmacological treatments. Chronic blockade of firing or synaptic activity reduced the remodeling process, in particular, branch addition in the target layer. However, extension of branches was not affected by this treatment. Together, these findings suggest that neural activity can modify the molecular mechanisms that regulate lamina-specific TC axon branching.
利用丘脑和皮质的器官型共培养物,研究了丘脑皮质(TC)投射中轴突分支的靶点和活动依赖性机制。通过单细胞电穿孔法用增强型黄色荧光蛋白(EYFP)标记TC轴突,并通过共聚焦显微镜随时间进行观察。还随时间监测在多电极培养皿上生长的共培养物的放电活动变化。在体外第二周,当丘脑和皮质细胞的自发放电活动增加时,EYFP标记的TC轴突在皮质外植体的第4层及其周围表现出更多的分支形成。延时成像进一步表明,分支模式是通过添加和消除动态产生的,并且倾向于在靶层积累分支。为了研究神经活动与TC分支形成之间的关系,在各种药物处理下分析了轴突分支的动态变化。慢性阻断放电或突触活动会减少重塑过程,特别是靶层中的分支添加。然而,分支的延伸不受此处理的影响。总之,这些发现表明神经活动可以改变调节层特异性TC轴突分支的分子机制。