Conti Emilia, Pavone Francesco Saverio, Allegra Mascaro Anna Letizia
Neuroscience Institute, National Research Council, Pisa, Italy.
European Laboratory for Non-Linear Spectroscopy, Sesto Fiorentino, Italy.
Methods Mol Biol. 2023;2616:69-81. doi: 10.1007/978-1-0716-2926-0_8.
The comprehension of the finest mechanisms underlying experience-dependent plasticity requires the investigation of neurons and synaptic terminals in the intact brain over prolonged periods of time. Longitudinal two-photon imaging together with the expression of fluorescent proteins enables high-resolution imaging of dendritic spines and axonal varicosities of cortical neurons in vivo. Importantly, the study of the mechanisms of structural reorganization is relevant for a deeper understanding of the pathophysiological mechanisms of neurological diseases such as stroke and for the development of new therapeutic approaches. This protocol describes the principal steps for in vivo investigation of neuronal plasticity both in healthy conditions and after an ischemic lesion. First, we give a description of the surgery to perform a stable cranial window that allows optical access to the mouse brain cortex. Then we explain how to perform longitudinal two-photon imaging of dendrites, axonal branches, and synaptic terminals in the mouse brain cortex in vivo, in order to investigate the plasticity of synaptic terminals and orientation of neuronal processes. Finally, we describe how to induce an ischemic lesion in a target region of the mouse brain cortex through a cranial window by applying the photothrombotic stroke model.
要理解经验依赖性可塑性背后的精妙机制,需要在完整大脑中对神经元和突触终末进行长时间的研究。纵向双光子成像结合荧光蛋白的表达能够对体内皮质神经元的树突棘和轴突膨体进行高分辨率成像。重要的是,对结构重组机制的研究有助于更深入地理解中风等神经疾病的病理生理机制,并推动新治疗方法的开发。本方案描述了在健康状态和缺血性损伤后对神经元可塑性进行体内研究的主要步骤。首先,我们描述了为形成一个稳定的颅窗以便光学观察小鼠大脑皮质而进行的手术。然后我们解释如何在体内对小鼠大脑皮质中的树突、轴突分支和突触终末进行纵向双光子成像,以研究突触终末的可塑性和神经元突起的方向。最后,我们描述了如何通过应用光血栓性中风模型,经颅窗在小鼠大脑皮质的目标区域诱导缺血性损伤。