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在活神经元中应用金纳米探针进行表型分类、连接性评估和电生理记录的体外研究。

Invitro application of gold nanoprobes in live neurons for phenotypical classification, connectivity assessment, and electrophysiological recording.

机构信息

Department of Biology, College of William and Mary, Williamsburg, VA 23187, USA.

出版信息

Brain Res. 2010 Apr 14;1325:19-27. doi: 10.1016/j.brainres.2010.02.041. Epub 2010 Feb 17.

Abstract

Thermoregulatory neurons in the preoptic area of the anterior hypothalamus (POA) form synaptic networks, which affect responses that regulate body temperature. To characterize these pathways of activation, projections to effector control areas, like the dorsomedial hypothalamus (DMH), require labeling in live tissue slices. Traditional fluorescent dyes label axon terminals near an injection site, but unfortunately, also that of nearby fibers of passage. Here, we describe a novel methodology for retrograde labeling of neurons in vitro, which will allow for further electrophysiological recording. To determine if POA neurons project to the DMH, we have used nanometer-sized, gold nanoprobes, which provide for specific neuronal entry, via synapses in close proximity to the injection site. Upon neuronal entry, these nanoprobe complexes diffuse to the soma, where they are readily visualized and quantified. We found that conjugation of these gold nanoprobes with VGLUT-2 antibodies and polyethyleneimine (PEI) facilitates neuronal entry and a high level of labeling efficacy. This novel method, adapted from emerging cancer therapy technologies, is highly specific for determining axon terminal projections within particular neuronal populations, while maintaining neuronal viability for targeted live cell electrophysiological recording.

摘要

下丘脑前区视前区的温度调节神经元形成突触网络,影响调节体温的反应。为了描述这些激活途径,需要对效应器控制区域(如背内侧下丘脑(DMH))的投射进行标记,这需要在活体组织切片中进行。传统的荧光染料标记注射部位附近的轴突末梢,但不幸的是,也标记了附近经过的纤维。在这里,我们描述了一种新的体外逆行标记神经元的方法,这将允许进一步进行电生理记录。为了确定视前区神经元是否投射到 DMH,我们使用了纳米级的金纳米探针,通过靠近注射部位的突触,这些探针特异性进入神经元。进入神经元后,这些纳米探针复合物扩散到胞体,在那里可以很容易地观察到并进行定量。我们发现,将这些金纳米探针与 VGLUT-2 抗体和聚乙烯亚胺(PEI)结合,有利于神经元进入和高水平的标记效率。这种新方法源自新兴的癌症治疗技术,高度特异性地确定特定神经元群体中的轴突末梢投射,同时保持神经元活力,以进行靶向活细胞电生理记录。

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