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基于图像的深度学习揭示了人类运动神经元对压力和 VCP 相关 ALS 的反应。

Image-based deep learning reveals the responses of human motor neurons to stress and VCP-related ALS.

机构信息

Genomics and Health Informatics Group, Idiap Research Institute, Martigny, Switzerland.

Human Stem Cells and Neurodegeneration Laboratory, The Francis Crick Institute, London, UK.

出版信息

Neuropathol Appl Neurobiol. 2022 Feb;48(2):e12770. doi: 10.1111/nan.12770. Epub 2021 Oct 18.

Abstract

AIMS

Although morphological attributes of cells and their substructures are recognised readouts of physiological or pathophysiological states, these have been relatively understudied in amyotrophic lateral sclerosis (ALS) research.

METHODS

In this study, we integrate multichannel fluorescence high-content microscopy data with deep learning imaging methods to reveal-directly from unsegmented images-novel neurite-associated morphological perturbations associated with (ALS-causing) VCP-mutant human motor neurons (MNs).

RESULTS

Surprisingly, we reveal that previously unrecognised disease-relevant information is withheld in broadly used and often considered 'generic' biological markers of nuclei (DAPI) and neurons ( III-tubulin). Additionally, we identify changes within the information content of ALS-related RNA binding protein (RBP) immunofluorescence imaging that is captured in VCP-mutant MN cultures. Furthermore, by analysing MN cultures exposed to different extrinsic stressors, we show that heat stress recapitulates key aspects of ALS.

CONCLUSIONS

Our study therefore reveals disease-relevant information contained in a range of both generic and more specific fluorescent markers and establishes the use of image-based deep learning methods for rapid, automated and unbiased identification of biological hypotheses.

摘要

目的

尽管细胞及其亚结构的形态特征被认为是生理或病理状态的读出器,但在肌萎缩侧索硬化症(ALS)研究中,这些特征相对研究较少。

方法

在这项研究中,我们将多通道荧光高内涵显微镜数据与深度学习成像方法相结合,直接从未分割的图像中揭示与(引起 ALS 的)VCP 突变型人类运动神经元(MNs)相关的新型神经突相关形态扰动。

结果

令人惊讶的是,我们发现以前未被识别的与疾病相关的信息被广泛使用的、通常被认为是核(DAPI)和神经元(III-微管蛋白)的“通用”生物标志物所掩盖。此外,我们还确定了在 VCP 突变型 MN 培养物中捕获到的与 ALS 相关的 RNA 结合蛋白(RBP)免疫荧光成像的信息内容发生了变化。此外,通过分析暴露于不同外在应激源的 MN 培养物,我们表明热应激再现了 ALS 的关键方面。

结论

因此,我们的研究揭示了一系列通用和更特定荧光标记物中包含的与疾病相关的信息,并确立了基于图像的深度学习方法用于快速、自动和无偏地识别生物学假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d9a/9298273/dc61584395ef/NAN-48-0-g005.jpg

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