Genetically encoded tools for Cell–Cell interactions underlying brain connectivity

Natsumi Hoshino , Takeshi Yagi , Takeharu Nagai , Takashi Kanadome
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Abstract

Brain development and function depend on complex yet organized neural networks and efficient communication between the neurons that form these networks. To understand the role of neural networks and communication between neurons, it is important to visualize interactions between neurons. In this review, we provide a comprehensive overview of visualization tools for cell–cell interactions, especially among neurons. We first introduce tools based on fluorescent protein technology that directly visualize cell–cell interactions, categorized into three different mechanisms: split fluorescent protein (split FP), dimerization-dependent fluorescent protein (ddFP), and Förster resonance energy transfer (FRET). Each type offers distinct advantages in terms of temporal resolution, reversibility, and spatial specificity, making them suitable for different experimental contexts within neural networks. Next, we introduce tools that indirectly visualize cell–cell interactions, based on a reporter system. Finally, we present several tools based on other mechanisms. By systematically comparing the performance and applicability of each tool, we provide a strategic framework for selecting appropriate tools based on experimental goals, ranging from short-lived synaptic interactions to long-term network connectivity studies.
大脑连接下细胞-细胞相互作用的基因编码工具
大脑的发育和功能依赖于复杂而有组织的神经网络以及构成这些网络的神经元之间的有效交流。为了理解神经网络的作用和神经元之间的交流,可视化神经元之间的相互作用是很重要的。在这篇综述中,我们提供了一个全面的概述可视化工具的细胞-细胞相互作用,特别是神经元之间。我们首先介绍了基于荧光蛋白技术的工具,直接可视化细胞-细胞相互作用,分为三种不同的机制:分裂荧光蛋白(分裂FP),二聚化依赖性荧光蛋白(ddFP)和Förster共振能量转移(FRET)。每种类型在时间分辨率、可逆性和空间特异性方面都具有独特的优势,使它们适用于神经网络中的不同实验环境。接下来,我们将介绍基于报告系统的间接可视化细胞-细胞相互作用的工具。最后,我们介绍了几种基于其他机制的工具。通过系统地比较每个工具的性能和适用性,我们提供了一个基于实验目标选择适当工具的战略框架,从短期突触相互作用到长期网络连接研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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