Non-invasive imaging of leukocyte homing and migration in vivo

Baomei Wang1, Bernd H Zinselmeyer, Jeremiah R McDole

  • 1Department of Pathology and Immunology, Washington University in St. Louis, USA.

Insights

This study introduces a non-invasive two-photon microscopy method for observing leukocyte trafficking in live mice. This technique avoids surgical preparation, enabling detailed study of immune cell movement in tissues.

Area of Science:

  • Immunology
  • Cell Biology
  • Biomedical Imaging

Background:

  • Two-photon (2P) microscopy offers high-resolution, spatiotemporal imaging of cell behaviors in live tissues.
  • Leukocyte recruitment is crucial for host defense but challenging to study in vivo due to rapid cell movement and light-scattering tissues.
  • Current intravital imaging often requires invasive surgical preparation, potentially causing artifacts.

Purpose of the Study:

  • To describe a novel, non-invasive single-cell imaging approach for studying leukocyte trafficking.
  • To enable in vivo visualization of leukocyte movement in the mouse footpad and phalanges without surgical intervention.
  • To provide a detailed guide on the technical aspects and experimental execution of this non-invasive 2P imaging preparation.

Main Methods:

  • Development and application of a non-invasive two-photon microscopy preparation.
  • Imaging leukocyte trafficking within the vasculature of the mouse footpad and phalanges.
  • Detailed description of experimental setup, execution, and data collection procedures.

Main Results:

  • Successful implementation of a non-invasive 2P imaging technique for observing leukocyte trafficking.
  • Demonstration of high-resolution, single-cell imaging of immune cell dynamics in intact mouse tissues.
  • Avoidance of surgical-induced tissue damage and inflammation, allowing for more natural observation of cell behavior.

Conclusions:

  • The described non-invasive 2P microscopy method provides a valuable tool for studying leukocyte trafficking in vivo.
  • This approach overcomes the limitations of surgical preparations, offering a less artifact-prone method for immunological research.
  • The technique facilitates detailed analysis of immune cell dynamics in specific anatomical locations like the mouse footpad.

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