Visualizing the fine structure and dynamics of living cells with temporal polychromatic digital holographic microscopy.

IF 1.4 3区 物理与天体物理 Q3 OPTICS
Mohamed Haouat, Céline Larivière-Loiselle, Marie-Ève Crochetière, Johan Chaniot, Maxime Moreaud, Erik Bélanger, Pierre Marquet
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引用次数: 0

Abstract

Polychromatic digital holographic microscopy (P-DHM) has demonstrated its capacity to generate highly denoised optical path difference images, thereby enabling the label-free visualization of fine cellular structures, such as the dendritic arborization within neuronal cells in culture. So far, however, the sample must remain more or less stationary since P-DHM is performed manually, i.e., all actions are carried out sequentially over several minutes. In this paper, we propose fully automated, robust, and efficient management of the acquisition and reconstruction of the time series of polychromatic hologram sets, transforming P-DHM into temporal P-DHM. Experimental results have demonstrated the ability of the proposed temporal P-DHM implementation to non-invasively and quantitatively reveal the fine structure and dynamics of living cells.

用时间多色数字全息显微镜观察活细胞的精细结构和动态。
多色数字全息显微镜(P-DHM)已经证明了其产生高度去噪的光程差图像的能力,从而使精细细胞结构的无标记可视化成为可能,例如培养神经元细胞内的树突状树突。然而,到目前为止,样品必须保持或多或少静止,因为P-DHM是手动执行的,即所有动作都是在几分钟内依次进行的。在本文中,我们提出了对多色全息图集合的时间序列的采集和重建进行全自动、鲁棒和高效的管理,将P-DHM转换为时间P-DHM。实验结果表明,所提出的时间P-DHM实现能够非侵入性和定量地揭示活细胞的精细结构和动力学。
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来源期刊
CiteScore
3.40
自引率
10.50%
发文量
417
审稿时长
3 months
期刊介绍: The Journal of the Optical Society of America A (JOSA A) is devoted to developments in any field of classical optics, image science, and vision. JOSA A includes original peer-reviewed papers on such topics as: * Atmospheric optics * Clinical vision * Coherence and Statistical Optics * Color * Diffraction and gratings * Image processing * Machine vision * Physiological optics * Polarization * Scattering * Signal processing * Thin films * Visual optics Also: j opt soc am a.
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