2018
DOI: 10.1002/cyto.a.23679
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Moving into a new dimension: Tracking migrating cells with digital holographic cytometry in 3D

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Cited by 6 publications
(6 citation statements)
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“…A more cell-friendly and speedy method of investigating morphological differences would facilitate CTC research. Digital holographic cytometry (DHC) is a powerful tool for label-free cell observations and the evaluation of cell morphological and dynamical parameters in vitro [20][21][22][23][24][25][26]. Studies using DHC include different cell types, from protozoa, bacteria and plant cells to mammalian cells such as nerve cells, stem cells and tumor cells [23].…”
Section: Introductionmentioning
confidence: 99%
“…A more cell-friendly and speedy method of investigating morphological differences would facilitate CTC research. Digital holographic cytometry (DHC) is a powerful tool for label-free cell observations and the evaluation of cell morphological and dynamical parameters in vitro [20][21][22][23][24][25][26]. Studies using DHC include different cell types, from protozoa, bacteria and plant cells to mammalian cells such as nerve cells, stem cells and tumor cells [23].…”
Section: Introductionmentioning
confidence: 99%
“…For the last decade, there have been significant developments in the instrumentations of QPI. [2,7,[11][12][13][14][15][16][17] For example, the spatial and temporal resolution of QPI had been improved and reached the limitations of farfield diffraction resolution and the speed of a high-speed image sensor. [18][19][20][21][22] Recently, many researchers have intensively reported biological applications of QPI, in particular, medical applications.…”
Section: Methods Detailsmentioning
confidence: 99%
“…Cell motility is an important feature as it is suggestive of invasiveness and, when monitored along organoid formation, arguably informs about the metastatic capacity of tumor cells [17]. Nonetheless, quantitative methods for studying these early events are scarce, as conventional migration assays such as wound-healing and transwell assays do not evaluate growth in 3D [18]. In turn, in vitro 3D cultures are commonly imaged using bright-field, fluorescence, or phase-contrast microscopy [19], where organoid formation is not continuously monitored.…”
Section: Discussionmentioning
confidence: 99%