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Updated: Sep 20, 2026

Ex vivo Imaging of T Cells in Murine Lymph Node Slices with Widefield and Confocal Microscopes
Published on: July 15, 2011
A stochastic view of lymphocyte motility and trafficking within the lymph node
Sindy H Wei1, Ian Parker, Mark J Miller
1Departments of Physiology and Biophysics, University of California, Irvine, CA 92697-4561, USA.
Insights
Two-photon microscopy reveals how lymphocytes move and recognize antigens in lymphoid organs. Random cell migration, not chemotaxis, may drive antigen recognition in native tissues.
Area of Science:
- Immunology
- Cell Biology
- Microscopy
Background:
- Lymphoid organs are critical for immune responses.
- Understanding lymphocyte behavior in vivo is essential for immunology.
- In vitro studies provide extensive data on lymphocyte motility and signaling.
Purpose of the Study:
- To review and analyze lymphocyte motility and antigen recognition in the native tissue environment.
- To compare in vivo findings with extensive in vitro literature.
- To propose a model for antigen recognition in lymphoid organs.
Main Methods:
- Utilizing two-photon microscopy for cellular dynamics in lymphoid organs.
- Analyzing three-dimensional images to understand cell migration mechanisms.
- Reviewing existing literature on lymphocyte motility, signaling, and chemotaxis in vitro.
Main Results:
- Two-photon microscopy offers insights into cellular dynamics within lymphoid organs.
- Analysis of 3D images elucidates mechanisms of cell migration and antigen recognition in vivo.
- In vivo observations are contrasted with a substantial body of in vitro data.
Conclusions:
- Lymphocyte random migration may facilitate a stochastic mechanism for antigen recognition in lymphoid organs.
- Antigen recognition in vivo might not be primarily guided by chemotaxis.
- The native tissue environment presents unique dynamics for lymphocyte function.
Abstract:
Two-photon microscopy is providing literal insight into the cellular dynamics of lymphoid organs and, guided by analysis of three-dimensional images, into mechanisms that underlie cell migration and antigen recognition in vivo. This review describes lymphocyte motility and antigen recognition in the native tissue environment and compares these results with a much more extensive literature on lymphocyte motility, signaling, and chemotaxis in vitro. We discuss the in vitro literature on dynamic aspects of lymphocyte motility, chemotaxis, and the response to antigen and present the view that random migration of lymphocytes may drive a stochastic mechanism of antigen recognition in lymphoid organs, rather than being guided by chemotaxis.
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