Live Microscopy

Live microscopy is the imaging of living cells, tissues, or organisms over time to observe biological structures and behaviors as they occur. It typically combines transmitted-light or fluorescence microscopy with time-lapse acquisition, allowing repeated image capture while controlled temperature, humidity, gas levels, and other conditions preserve specimen viability. By revealing cell migration, division, intracellular transport, developmental changes, and interactions between organisms and their environments, live microscopy connects structure with dynamic function. In biology, these observations support quantitative analysis of cellular processes, disease mechanisms, drug responses, and tissue development while reducing reliance on fixed, endpoint samples.

Live Microscopy - Related Videos

Research

JoVE Journal - Immunology and Infection
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Live-cell Video Microscopy of Fungal Pathogen Phagocytosis

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Cited by 22 •

2013

We describe methods for live-cell video microscopy of Candida albicans phagocytosis by macrophages. These methods enable stage-specific analysis of macrophage migration, recognition, engulfment and phagosome maturation and reveal novel aspects of phagocytosis.

Research

JoVE Journal - Bioengineering

Controlled Strain of 3D Hydrogels under Live Microscopy Imaging

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Cited by 5 •

2020

The presented method involves uniaxial stretching of 3D soft hydrogels embedded in silicone rubber while allowing live confocal microscopy. Characterization of the external and internal hydrogel strains as well as fiber alignment are demonstrated. The device and protocol developed can assess the response of cells to various strain regimes.

Live Imaging of the Zebrafish Embryonic Brain by Confocal Microscopy

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Cited by 27 •

2009

In this video, we demonstrate a method by which to analyze the developing vertebrate brain in live zebrafish embryos at single cell resolution by confocal microscopy. This includes the method by which we inject the single-cell zebrafish embryo and subsequently mount and image the developing brain.

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy

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Cited by 15 •

2012

Methods for purifying the cholesterol binding toxin streptolysin O from recombinant E. coli and visualization of toxin binding to live eukaryotic cells are described. Localized delivery of toxin induces rapid and complex changes in targeted cells revealing novel aspects of toxin biology.

Measuring the Mechanical Properties of Living Cells Using Atomic Force Microscopy

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Cited by 160 •

2013

This paper demonstrates a protocol to characterize the mechanical properties of living cells by means of microindentation using an Atomic Force Microscope (AFM).

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