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.

Immunological Reviews
|September 13, 2003
PubMed

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.

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