全息显微镜和相干控制全息显微镜的比较。

IF 1.5 4区 工程技术 Q3 MICROSCOPY Journal of microscopy Pub Date : 2024-01-10 DOI:10.1111/jmi.13260
Vera Chvalova, Tomas Vomastek, Tomas Grousl
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引用次数: 0

摘要

定量相位成像(QPI)是对活细胞进行无标记可视化的强大工具。在这里,我们比较了两种 QPI 显微镜--Telight Q-Phase 显微镜和 Nanolive 3D Cell Explorer-fluo 显微镜。这两种系统都能提供无偏见的细胞形态信息,如单个细胞的干质量、周长和面积。Q-Phase 显微镜采用无伪影、相干控制的全息成像技术实时观察细胞,光毒性极低。3D Cell Explorer-fluo利用激光全息成像技术重建活细胞的三维图像,直观显示其内部结构和动态。在这里,我们分析了这两种显微镜在观察两种形态截然不同的细胞系--形成多细胞团的立方上皮 MDCK 细胞和单生的 Rat2 成纤维细胞--时的优势和局限性。我们主要关注设备生成适合内置软件进行单细胞分割的图像的能力,并讨论了分割结果和从分割图像生成的定量数据。我们的研究表明,这两种显微镜的优势略有不同,如何选择取决于用户的具体要求和目标。
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Comparison of holotomographic microscopy and coherence-controlled holographic microscopy

Quantitative phase imaging (QPI) is a powerful tool for label-free visualisation of living cells. Here, we compare two QPI microscopes – the Telight Q-Phase microscope and the Nanolive 3D Cell Explorer-fluo microscope. Both systems provide unbiased information about cell morphology, such as individual cell dry mass, perimeter and area. The Q-Phase microscope uses artefact-free, coherence-controlled holographic imaging technology to visualise cells in real time with minimal phototoxicity. The 3D Cell Explorer-fluo employs laser-based holotomography to reconstruct 3D images of living cells, visualising their internal structures and dynamics. Here, we analysed the strengths and limitations of both microscopes when examining two morphologically distinct cell lines – the cuboidal epithelial MDCK cells which form multicellular clusters and solitary growing Rat2 fibroblasts. We focus mainly on the ability of the devices to generate images suitable for single-cell segmentation by the built-in software, and we discuss the segmentation results and quantitative data generated from the segmented images. We show that both microscopes offer slightly different advantages, and the choice between them depends on the specific requirements and goals of the user.

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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
期刊介绍: The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit. The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens. Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.
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