Intravital Microscopy
Intravital Microscopy - Related Videos
10:07
Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
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2014
High-resolution intravital imaging with enhanced contrast up to 120 µm depth in lymph nodes of adult mice is achieved by spatially modulating the excitation pattern of a multi-focal two-photon microscope. In 100 µm depth we measured resolutions of 487 nm (lateral) and 551 nm (axial), thus circumventing scattering and diffraction limits.
11:36
Intravital Microscopy of the Spleen: Quantitative Analysis of Parasite Mobility and Blood Flow
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Cited by 17 •
2012
We show the method for performing intravital microscopy of the spleen using GFP transgenic malaria parasites and the quantification of parasite mobility and blood flow within this organ.
08:37
Intravital Microscopy of the Mouse Brain Microcirculation using a Closed Cranial Window
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Cited by 37 •
2010
Intravital microscopy to follow temporal and spatial hemodynamic and inflammatory events in the pial microcirculation.
05:54
Intravital Fluorescence Microscopy to Study Microvascular Thrombus Formation
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2025
This video demonstrates the intravital fluorescence microscopy technique to study thrombus formation in a mouse model. The mouse is injected with a fluorophore-labeled polysaccharide to monitor blood circulation. Upon illumination with a high-intensity light, the phototoxic induction of an injury in the microvasculature of the ear leads to the formation of a thrombus, which is confirmed by visualizing the obstruction in the blood flow.
09:01
Intravital Microscopy and Thrombus Induction in the Earlobe of a Hairless Mouse
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Cited by 4 •
2017
The ear model of the hairless SKH1-Hrhr mouse enables intravital fluorescence microscopy of microcirculation and phototoxic thrombus induction without prior surgical preparation in the examined microvascular bed. Therefore, the ear of the hairless mouse is an excellent in vivo model to study the complex interactions during microvascular thrombus formation, thrombus evolution, and thrombolysis.
FAQs
These approaches provide complementary ways to visualize activity in living organisms. Fluorescent labels and vital reporters add signals that can identify cellular or molecular events, whereas label-free contrast relies on optical differences without adding a signal. Choosing among them affects what biological activity can be followed and how the resulting images are interpreted.
Multiphoton microscopy and tissue windows address different parts of the imaging problem. The optical system supports image collection, while a transparent window or exposed tissue provides access to the living region of interest. Together, they allow measurements to remain connected to physiological context, which is essential when interpreting cell behavior, blood flow, or tissue remodeling.
Fixed-tissue imaging provides a static view, whereas intravital measurements can follow the same biological setting over time. That temporal perspective helps reveal treatment responses and biological heterogeneity while preserving relationships among cells, blood flow, immune interactions, and tissue remodeling during observation. These features make dynamic processes accessible rather than limiting analysis to a single endpoint.
Tracking cells and molecular activity alongside blood flow, immune interactions, or tissue remodeling creates a basis for relating visible behavior to underlying mechanisms. Rather than treating an image as an isolated endpoint, researchers can examine how events develop during disease progression or tissue change. This linkage is valuable when cellular behavior must be interpreted within its surrounding physiological context.
A typical setup combines an imaging target in a living organism, a signal source such as a fluorescent label or vital reporter, and an optical system capable of collecting images. Researchers may image through a transparent window or exposed tissue, or use label-free contrast. The selected combination determines how cellular and molecular activity is recorded.
Its applications span cancer, inflammation, neuroscience, development, and regenerative biology. In each setting, the method can preserve physiological context while researchers examine processes such as immune interactions, tissue remodeling, blood flow, or disease progression. This breadth makes it useful for connecting cellular and molecular activity with changes occurring at the tissue or organism level.
Longitudinal measurements can show how disease progression changes over time and how biological activity responds to treatment. They can also reveal heterogeneity, meaning that responses or behaviors differ across observations within a biological system. These outcomes help researchers move beyond a single endpoint when evaluating dynamic biology and assessing changes in living tissues.