Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, via Morego 30 16163 Genova.
Sci Rep. 2011;1:183. doi: 10.1038/srep00183. Epub 2011 Dec 6.
During development, axons of neurons in the mammalian central nervous system lose their ability to regenerate. To study the regeneration process, axons of mouse hippocampal neurons were partially damaged by an UVA laser dissector system. The possibility to deliver very low average power to the sample reduced the collateral thermal damage and allowed studying axonal regeneration of mouse neurons during early days in vitro. Force spectroscopy measurements were performed during and after axon ablation with a bead attached to the axonal membrane and held in an optical trap. With this approach, we quantified the adhesion of the axon to the substrate and the viscoelastic properties of the membrane during regeneration. The reorganization and regeneration of the axon was documented by long-term live imaging. Here we demonstrate that BDNF regulates neuronal adhesion and favors the formation of actin waves during regeneration after axonal lesion.
在哺乳动物中枢神经系统的发育过程中,神经元的轴突丧失了再生的能力。为了研究再生过程,使用 UVA 激光解剖系统部分损伤了小鼠海马神经元的轴突。将非常低的平均功率传递到样品中的可能性降低了旁侧热损伤,并允许在体外早期研究小鼠神经元的轴突再生。在用附着在轴突膜上的珠子固定在光阱中进行轴突消融期间和之后进行力谱测量。通过这种方法,我们定量测量了轴突与基底的粘附力以及再生过程中膜的粘弹性。通过长期活细胞成像记录了轴突的重组和再生。在这里,我们证明了 BDNF 调节神经元的粘附,并在轴突损伤后的再生过程中有利于肌动蛋白波的形成。