使用高通量显微镜和基于深度学习的细胞识别算法Cellpose跟踪纳米颗粒被细胞摄取

IF 4.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Frontiers in Nanotechnology Pub Date : 2023-05-18 DOI:10.3389/fnano.2023.1181362
Boxuan Yang, Ceri J Richards, Timea B Gandek, Isa de Boer, Itxaso Aguirre-Zuazo, Else Niemeijer, Christoffer Åberg
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引用次数: 0

摘要

人类细胞吸收了多少纳米颗粒是医学和安全领域许多应用的关键问题。虽然已经开发并应用了许多方法来解决这个问题,但基于显微镜的方法具有一些独特的优势。然而,显微镜的费力性质,特别是随之而来的图像分析,仍然是一个瓶颈。自动图像分析一直在寻求解决这种情况,但也带来了自身的挑战。在这里,我们在HeLa细胞的荧光显微镜图像上测试了最近开发的基于深度学习的细胞识别算法Cellpose。我们发现该算法表现非常好,因此开发了一个工作流程,使我们能够在相对适中的时间内获取和分析数千个细胞,而不会牺牲细胞识别的准确性。随后,我们在暴露于荧光标记的聚苯乙烯纳米颗粒的细胞图像上测试了工作流程。然后,该数据集被用于研究细胞大小和纳米颗粒摄取之间的关系,高通量显微镜在这一主题上特别有用。
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Following nanoparticle uptake by cells using high-throughput microscopy and the deep-learning based cell identification algorithm Cellpose
How many nanoparticles are taken up by human cells is a key question for many applications, both within medicine and safety. While many methods have been developed and applied to this question, microscopy-based methods present some unique advantages. However, the laborious nature of microscopy, in particular the consequent image analysis, remains a bottleneck. Automated image analysis has been pursued to remedy this situation, but offers its own challenges. Here we tested the recently developed deep-learning based cell identification algorithm Cellpose on fluorescence microscopy images of HeLa cells. We found that the algorithm performed very well, and hence developed a workflow that allowed us to acquire, and analyse, thousands of cells in a relatively modest amount of time, without sacrificing cell identification accuracy. We subsequently tested the workflow on images of cells exposed to fluorescently-labelled polystyrene nanoparticles. This dataset was then used to study the relationship between cell size and nanoparticle uptake, a subject where high-throughput microscopy is of particular utility.
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来源期刊
Frontiers in Nanotechnology
Frontiers in Nanotechnology Engineering-Electrical and Electronic Engineering
CiteScore
7.10
自引率
0.00%
发文量
96
审稿时长
13 weeks
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