Dynamic Live Imaging

Dynamic live imaging is the time-resolved visualization of living cells, tissues, or engineered biological systems as they change, providing information that static images cannot capture. It typically combines microscopy with fluorescent labels, controlled environmental conditions, and repeated image acquisition to track processes such as cell movement, growth, signaling, or structural remodeling without interrupting the sample. In bioengineering, these measurements help researchers evaluate tissue development, biomaterial interactions, organoid behavior, and cell-based therapies. Quantitative analysis of image sequences can reveal temporal patterns and mechanistic relationships, supporting the design of more reliable engineered systems and improving understanding of dynamic biological function.

Dynamic Live Imaging - Related Videos

Research

JoVE Journal - Cancer Research

Live Imaging to Study Microtubule Dynamic Instability in Taxane-resistant Breast Cancers

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Cited by 3 •

2017

In this paper, we report a protocol describing an in vivo method to measure microtubule dynamic instability in docetaxel-resistant breast cancer cells (MCF-7TXT). In this method, a deconvolution microscopy imaging system is used to detect the expression of GFP-tubulin in target cells.

Live Cell Imaging of F-actin Dynamics via Fluorescent Speckle Microscopy (FSM)

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Cited by 8 •

2009

Selection, microinjection, and imaging of fluorescently-labeled F-actin via fluorescent speckle microscopy (FSM).

Visualization of Endosome Dynamics in Living Nerve Terminals with Four-dimensional Fluorescence Imaging

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2014

Four-dimensional (4D) imaging is utilized to study the behavior and interactions among two types of endosomes in living vertebrate nerve terminals. Movement of these small structures is characterized in three dimensions, permitting confirmation of events such as endosome fusion and exocytosis.

Use of an Optical Trap for Study of Host-Pathogen Interactions for Dynamic Live Cell Imaging

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Cited by 8 •

2011

A method is described to individually select, manipulate, and image live pathogens using an optical trap coupled to a spinning disk microscope. The optical trap provides spatial and temporal control of organisms and places them adjacent to host cells. Fluorescence microscopy captures dynamic intercellular interactions with minimal perturbation to cells.

Research

JoVE Journal - Immunology and Infection
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Live Imaging and Characterization of Microglia Dynamics in the Zebrafish Embryo

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Cited by 2 •

2024

We demonstrate a method that takes advantage of fast scanning confocal microscopy to perform live imaging of microglia cells in the developing zebrafish optic tectum, allowing for the analysis of the dynamics of these cells in vivo.

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