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T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
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Functional Brain Systems: Reticular Formation01:13

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Related Experiment Video

Updated: May 27, 2026

Real-Time In Vitro Migration Assay for Primary Murine CD8+ T Cells
06:42

Real-Time In Vitro Migration Assay for Primary Murine CD8+ T Cells

Published on: May 24, 2024

T-cell movement on the reticular network.

Graham M Donovan1, Grant Lythe

  • 1Department of Mathematics, University of Auckland, Auckland, New Zealand. g.donovan@auckland.ac.nz

Journal of Theoretical Biology
|November 22, 2011
PubMed
Summary
This summary is machine-generated.

T cell movement in lymph nodes may follow a reticular network (RN). Mathematical models show constant speed motion along RN edges aligns with observed T cell behavior, but doesn't increase cell encounters.

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Ex vivo Imaging of T Cells in Murine Lymph Node Slices with Widefield and Confocal Microscopes
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Ex vivo Imaging of T Cells in Murine Lymph Node Slices with Widefield and Confocal Microscopes
09:45

Ex vivo Imaging of T Cells in Murine Lymph Node Slices with Widefield and Confocal Microscopes

Published on: July 15, 2011

Area of Science:

  • Immunology
  • Biophysics
  • Computational Biology

Background:

  • T cell random motion in lymph nodes is hypothesized to occur on a reticular network (RN).
  • Previous dynamic imaging and theoretical studies support the RN hypothesis for T cell trafficking.

Purpose of the Study:

  • To develop a mathematical model of the reticular network (RN) in lymph nodes.
  • To simulate lymphocyte movement on this RN model to understand T cell migration patterns.

Main Methods:

  • Created a 3D mathematical representation of the RN with randomly distributed vertices and edges.
  • Modeled lymphocyte movement using constant speed along edges and edge-confined Brownian motion.
  • Analyzed mean-squared displacement and turning angle distributions.

Main Results:

  • Constant speed motion along RN edges is consistent with observed T cell mean-squared displacement over time.
  • Movement restricted to the RN results in a non-random distribution of turning angles.
  • Confining T cell movement to the network does not inherently increase cell-cell encounter frequency.

Conclusions:

  • The reticular network model provides a plausible explanation for T cell migration patterns in lymph nodes.
  • Lymphocyte movement dynamics on a network are characterized by specific turning angle distributions.
  • Network confinement alone does not enhance T cell interaction rates within lymph nodes.