Two-photon Imaging of Synaptic Plasticity and Pathology in the Living Mouse Brain

Jaime Grutzendler , Wen-Biao Gan
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引用次数: 22

Abstract

Two–photon microscopy (TPM) has become an increasingly important tool for imaging the structure and function of brain cells in living animals. TPM imaging studies of neuronal structures over intervals ranging from seconds to years have begun to provide important insights into the structural plasticity of synapses and the modulating effects of experience in the intact brain. TPM has also started to reveal how neuronal connections are altered in animal models of neurodegeneration, acute brain injury, and cerebrovascular disease. Here, we review some of these studies with special emphasis on the degree of structural dynamism of postsynaptic dendritic spines in the adult mouse brain as well as synaptic pathology in mouse models of Alzheimer’s disease and cerebral ischemia. We also discuss technical considerations that are critical for the acquisition and interpretation of data from TPM in vivo.

活体小鼠脑突触可塑性和病理的双光子成像
双光子显微镜(TPM)已成为活体动物脑细胞结构和功能成像的重要工具。从几秒到几年的时间间隔内对神经元结构的TPM成像研究已经开始为突触的结构可塑性和完整大脑中经验的调节作用提供重要的见解。TPM也开始揭示神经变性、急性脑损伤和脑血管疾病动物模型中的神经元连接是如何改变的。在此,我们回顾了其中的一些研究,特别强调了成年小鼠脑突触后树突棘的结构动力程度,以及阿尔茨海默病和脑缺血小鼠模型的突触病理学。我们还讨论了对体内TPM数据的获取和解释至关重要的技术考虑。
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