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全氟萘烷对微电极阵列上神经元组织的绝缘压缩增强了电生理测量。

Insulative Compression of Neuronal Tissues on Microelectrode Arrays by Perfluorodecalin Enhances Electrophysiological Measurements.

作者信息

Duenki Tomoya, Ikeuchi Yoshiho

机构信息

Institute of Industrial Science, The University of Tokyo, Meguro, Tokyo, 153-8505, Japan.

Institute for AI and Beyond, The University of Tokyo, Bunkyo, Tokyo, 113-8655, Japan.

出版信息

Adv Healthc Mater. 2025 Mar;14(6):e2403771. doi: 10.1002/adhm.202403771. Epub 2025 Jan 5.

DOI:10.1002/adhm.202403771
PMID:39757474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11874680/
Abstract

Microelectrode array (MEA) techniques provide a powerful method for exploration of neural network dynamics. A critical challenge is to interface 3D neural tissues including neural organoids with the flat MEAs surface, as it is essential to place neurons near to the electrodes for recording weak extracellular signals of neurons. To enhance performance of MEAs, most research have focused on improving their surface treatment, while little attention has been given to improve the tissue-MEA interactions from the medium side. Here, a strategy is introduced to augment MEA measurements by overlaying perfluorodecalin (PFD), a biocompatible fluorinated solvent, over neural tissues. Laying PFD over cerebral organoids insulates and compresses the tissues on MEA, which significantly enhances electrophysiological recordings. Even subtle signals such as the propagation of action potentials in bundled axons of motor nerve organoids can be detected with the technique. Moreover, PFD stabilizes tissues in acute recordings and its transparency allows optogenetic manipulations. This research highlights the potential of PFD as a tool for refining electrophysiological measurements of in vitro neuronal cultures. This can open new avenues to leverage precision of neuroscientific investigations and expanding the toolkit for in vitro studies of neural function and connectivity.

摘要

微电极阵列(MEA)技术为探索神经网络动力学提供了一种强大的方法。一个关键挑战是将包括神经类器官在内的三维神经组织与MEA的平面表面连接起来,因为将神经元放置在靠近电极的位置对于记录神经元微弱的细胞外信号至关重要。为了提高MEA的性能,大多数研究都集中在改善其表面处理,而很少关注从中等层面改善组织与MEA的相互作用。在此,引入了一种策略,即通过在神经组织上覆盖全氟萘烷(PFD,一种生物相容性氟化溶剂)来增强MEA测量。在脑类器官上铺设PFD可使组织在MEA上绝缘并压缩,这显著增强了电生理记录。即使是诸如运动神经类器官的成束轴突中动作电位传播等细微信号也可以用该技术检测到。此外,PFD在急性记录中能稳定组织,其透明度允许进行光遗传学操作。这项研究突出了PFD作为一种改进体外神经元培养电生理测量工具的潜力。这可以开辟新途径,以利用神经科学研究的精确性并扩展用于神经功能和连通性体外研究的工具包。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/912288c5596f/ADHM-14-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/1cecf5a3ce33/ADHM-14-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/3d554ca5b22d/ADHM-14-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/08285190af29/ADHM-14-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/a49ef7c480e1/ADHM-14-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/912288c5596f/ADHM-14-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/1cecf5a3ce33/ADHM-14-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/3d554ca5b22d/ADHM-14-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/08285190af29/ADHM-14-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/a49ef7c480e1/ADHM-14-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a480/11874680/912288c5596f/ADHM-14-0-g002.jpg

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