In Vivo Microscopy

In vivo microscopy is the imaging of living organisms, tissues, or cells in their native physiological environment, preserving dynamic biological activity that fixed-sample methods cannot capture. In neuroscience, optical techniques such as two-photon microscopy use focused near-infrared excitation to image fluorescent indicators through scattering tissue, often while animals perform behavioral tasks; repeated imaging can track the same structures over time. These approaches reveal neuronal activity, synaptic remodeling, vascular responses, and glial dynamics with cellular or subcellular resolution. By linking brain physiology to behavior and disease progression, in vivo microscopy supports studies of circuit function, plasticity, neurodegeneration, and responses to therapeutic interventions.

In Vivo Microscopy - Related Videos

Research

JoVE Journal - Neuroscience

In vivo Imaging of the Mouse Spinal Cord Using Two-photon Microscopy

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Cited by 42 •

2012

A minimally invasive protocol to stabilize the mouse spinal column and perform repetitive in vivo spinal cord imaging using two-photon microscopy is described. This method combines a spinal stabilization device and an anesthetic regimen to minimize respiratory-induced movements and produce raw imaging data that require no alignment or other post-processing.

Measuring the Stiffness of Ex Vivo Mouse Aortas Using Atomic Force Microscopy

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Cited by 26 •

2016

We present detailed protocols for isolation of aortas from mouse and measurement of their elastic modulus using atomic force microscopy.

In Vivo Two-Photon Microscopy of Single Nerve Endings in Skin

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Cited by 13 •

2014

The protocol for dynamic longitudinal imaging and selective laser lesion of nerve endings in reporter transgenic mice is...

In vivo Clonal Tracking of Hematopoietic Stem and Progenitor Cells Marked by Five Fluorescent Proteins using Confocal and Multiphoton Microscopy

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Cited by 11 •

2014

Combinatorial 5 fluorescent proteins marking of hematopoietic stem and progenitor cells allows in vivo clonal tracking via confocal and two-photon microscopy, providing insights into bone marrow hematopoietic architecture during regeneration. This method allows non-invasive fate mapping of spectrally-coded HSPCs-derived cells in intact tissues for extensive periods of time following transplantation.

In vivo Micro-circulation Measurement in Skeletal Muscle by Intra-vital Microscopy

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Cited by 5 •

2007

A new versatile method for observation of microcirculation is presented. It is considered suitable for long-term observation, and for combination with pharmacophysiological or molecular biological interventions.

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