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在行为水螅中以单细胞分辨率自动监测神经活动。

Automatic monitoring of neural activity with single-cell resolution in behaving Hydra.

机构信息

Department of Biological Sciences, Neurotechnology Center, Columbia University, New York, NY, USA.

Department of Psychiatry, New York State Psychiatric Institute, Columbia University, New York, NY, USA.

出版信息

Sci Rep. 2024 Mar 1;14(1):5083. doi: 10.1038/s41598-024-55608-2.

Abstract

The ability to record every spike from every neuron in a behaving animal is one of the holy grails of neuroscience. Here, we report coming one step closer towards this goal with the development of an end-to-end pipeline that automatically tracks and extracts calcium signals from individual neurons in the cnidarian Hydra vulgaris. We imaged dually labeled (nuclear tdTomato and cytoplasmic GCaMP7s) transgenic Hydra and developed an open-source Python platform (TraSE-IN) for the Tracking and Spike Estimation of Individual Neurons in the animal during behavior. The TraSE-IN platform comprises a series of modules that segments and tracks each nucleus over time and extracts the corresponding calcium activity in the GCaMP channel. Another series of signal processing modules allows robust prediction of individual spikes from each neuron's calcium signal. This complete pipeline will facilitate the automatic generation and analysis of large-scale datasets of single-cell resolution neural activity in Hydra, and potentially other model organisms, paving the way towards deciphering the neural code of an entire animal.

摘要

记录行为动物中每个神经元的每个尖峰的能力是神经科学的圣杯之一。在这里,我们通过开发一个端到端的管道,自动跟踪和提取刺胞动物海葵(Hydra vulgaris)中单个神经元的钙信号,朝着这个目标又迈进了一步。我们对双标记(核 tdTomato 和细胞质 GCaMP7s)的转基因海葵进行成像,并开发了一个用于在动物行为过程中跟踪和估计单个神经元的开源 Python 平台(TraSE-IN)。TraSE-IN 平台由一系列模块组成,这些模块可随时间对每个细胞核进行分割和跟踪,并提取 GCaMP 通道中的相应钙活性。另一系列信号处理模块可从每个神经元的钙信号中稳健地预测单个尖峰。这个完整的管道将促进在海葵中自动生成和分析大规模单细胞分辨率神经活动数据集,并且可能在其他模式生物中也适用,为破译整个动物的神经密码铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e2/10907378/19228299dfd8/41598_2024_55608_Fig1_HTML.jpg

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