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神经元回路的纳米级图案化

Nanoscale Patterning of Neuronal Circuits.

作者信息

Mateus José C, Weaver Sean, van Swaay Dirk, Renz Aline F, Hengsteler Julian, Aguiar Paulo, Vörös János

机构信息

Neuroengineering and Computational Neuroscience Laboratory, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.

Laboratory for Biosensors and Bioelectronics, ETH Zürich, 8092 Zürich, Switzerland.

出版信息

ACS Nano. 2022 Apr 26;16(4):5731-5742. doi: 10.1021/acsnano.1c10750. Epub 2022 Apr 11.

Abstract

Methods for patterning neurons have gradually improved and are used to investigate questions that are difficult to address or . Though these techniques guide axons between groups of neurons, multiscale control of neuronal connectivity, from circuits to synapses, is yet to be achieved As studying neuronal circuits with synaptic resolution poses significant challenges, we present an alternative to validate biophysical and computational models. In this work we use a combination of electron beam lithography and photolithography to create polydimethylsiloxane (PDMS) structures with features ranging from 150 nm to a few millimeters. Leveraging the difference between average axon and dendritic spine diameters, we restrict axon growth while allowing spines to pass through nanochannels to guide synapse formation between small groups of neurons (i.e., nodes). We show this technique can be used to generate large numbers of isolated feed-forward circuits where connections between nodes are restricted to regions connected by nanochannels. Using a genetically encoded calcium indicator in combination with fluorescently tagged postsynaptic protein, PSD-95, we demonstrate functional synapses can form in this region.

摘要

神经元图案化方法已逐渐改进,并用于研究难以解决的问题。尽管这些技术可引导轴突在神经元群之间生长,但从神经回路到突触的神经元连接性的多尺度控制仍未实现。由于以突触分辨率研究神经回路面临重大挑战,我们提出了一种验证生物物理和计算模型的替代方法。在这项工作中,我们结合使用电子束光刻和光刻技术来创建聚二甲基硅氧烷(PDMS)结构,其特征尺寸范围从150纳米到几毫米。利用平均轴突和树突棘直径的差异,我们限制轴突生长,同时允许树突棘穿过纳米通道,以引导小群神经元(即节点)之间的突触形成。我们表明,该技术可用于生成大量孤立的前馈回路,其中节点之间的连接仅限于由纳米通道连接的区域。结合使用基因编码的钙指示剂和荧光标记的突触后蛋白PSD-95,我们证明了该区域可以形成功能性突触。

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