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完整分离的新皮质和海马标本及其在成像研究中的应用。

Whole isolated neocortical and hippocampal preparations and their use in imaging studies.

作者信息

Davies Melissa L, Kirov Sergei A, Andrew R David

机构信息

Department of Anatomy & Cell Biology and The Centre for Neuroscience Studies, Queen's University, Kingston, Ont., Canada.

出版信息

J Neurosci Methods. 2007 Nov 30;166(2):203-16. doi: 10.1016/j.jneumeth.2007.07.012. Epub 2007 Jul 25.

Abstract

This study shows that two whole isolated preparations from the young mouse, the neocortical 'slab' and the hippocampal formation, are useful for imaging studies requiring both global monitoring using light transmittance (LT) imaging and high resolution cellular monitoring using 2-photon laser scanning microscopy (2PLSM). These preparations share advantages with brain slices such as maintaining intrinsic neuronal properties and avoiding cardiac or respiratory movement. Important additional advantages include the maintenance of all local input and output pathways, the absence of surfaces injured by slicing and the preservation of three-dimensional tissue structure. Using evoked extracellular field recording, we demonstrate long-term (hours) viability of both whole preparations. We then show that propagating cortical events such as anoxic depolarization (AD) and spreading depression (SD) can be imaged in both preparations, yielding results comparable to those in brain slices but retaining the tissue's three-dimensional structure. Using transgenic mice expressing green fluorescent protein (GFP) in pyramidal and granule cell neurons, 2PLSM confirms that these preparations are free of the surface damage observed in sliced brain tissue. Moreover the neurons undergo swelling with accompanying dendritic beading following AD induced by simulated ischemia, similar to cortical damage described in vivo.

摘要

本研究表明,从小鼠幼体获取的两种完整分离标本,即新皮质“薄片”和海马结构,对于需要同时使用透光率(LT)成像进行整体监测以及使用双光子激光扫描显微镜(2PLSM)进行高分辨率细胞监测的成像研究很有用。这些标本与脑片具有共同优点,如保持神经元固有特性以及避免心脏或呼吸运动。重要的额外优点包括维持所有局部输入和输出通路、不存在切片造成的表面损伤以及保留三维组织结构。通过诱发细胞外场记录,我们证明了两种完整标本的长期(数小时)活力。然后我们表明,诸如缺氧去极化(AD)和扩散性抑制(SD)等传播性皮质事件在两种标本中均可成像,产生的结果与脑片中的结果相当,但保留了组织的三维结构。使用在锥体细胞和颗粒细胞神经元中表达绿色荧光蛋白(GFP)的转基因小鼠,2PLSM证实这些标本不存在切片脑组织中观察到的表面损伤。此外,在模拟缺血诱导的AD后,神经元会肿胀并伴有树突串珠形成,类似于体内描述的皮质损伤。

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