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

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.

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Publication Details

Journal
Journal of the Optical Society of America A
Published
2024-10-03
DOI
https://doi.org/10.1364/josaa.534150
Citations
6
Primary Topic
Digital Holography and Microscopy
Type
article
Field-Weighted Citation Impact
2.03

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article

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

Maxime Moreaud, Johan Chaniot, Marie‐Ève Crochetière, Mohamed Haouat et al.
6 citations
Journal of the Optical Society of America A
Digital Holography and Microscopy
2.03
article

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

Maxime Moreaud, Johan Chaniot, Marie‐Ève Crochetière, Mohamed Haouat, Erik Bélanger, Céline Larivière-Loiselle, Pierre Marquet
article en
6 citations

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.

Journal of the Optical Society of America AVol. 41(11)
IFP Énergies nouvelles (FR), Centre Hospitalier Universitaire Vaudois (CH), Concello de Cervo (ES), Université Laval (CA), University of Lausanne (CH)
Québec Consortium for Drug Discovery, Canada Foundation for Innovation, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 13%
Digital Holography and Microscopy
2.03
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