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T Cell Activation and Clonal Selection01:22

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.
Naive T cells that have not yet encountered an antigen express two primary CD...
Cell-matrix's Response to Mechanical Forces01:13

Cell-matrix's Response to Mechanical Forces

In animal cells, the extracellular matrix allows cells within tissues to withstand external stresses and transmits signals from the outside of the cell to the inside. The extracellular matrix is extensive, and its composition varies between different types of tissues. For example, the reticular fibers and ground substance make up the ECM in loose connective tissue, while collagen and bone minerals make up the ECM of bone tissue. 
Anchoring junctions mechanically attach a cell to the...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
Mechanically-gated Ion Channels01:12

Mechanically-gated Ion Channels

Mechanically-gated ion channels are proteins found in eukaryotic and prokaryotic cell membranes that open in response to mechanical stress. Tension, compression, swelling, and shear stress can alter the conformation of the protein, opening a transmembrane channel that allows the passage of ions for signal transmission. In eukaryotes, mechanically-gated channels are distributed in several regions like the neurons, lungs, skin, bladder, and heart, where they play critical roles in numerous...
Tension Response at Adherens Junctions01:26

Tension Response at Adherens Junctions

The adherens junctions that anchor cells together are multi-protein complexes that dynamically adapt to mechanical stimuli such as tensile forces and shear stress. Mechanosensory proteins in these junctions can sense such mechanical stimuli and undergo a shift in their conformation, resulting in an altered function — a process called mechanotransduction.
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin homology) domains...
Activation of Integrins01:15

Activation of Integrins

Integrins bind ligands and transmit information from outside the cell to inside or vice-versa through an "outside-in signaling" or "inside-out signaling."
In "outside-in signaling," external factors in the extracellular space bind to exposed ligand binding sites on integrins. This causes the inactive protein to undergo a conformational change to become active. Integrins are often clustered on the cell membrane. Repetitive and regularly spaced ligand binding events provide an effective stimulus.

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Updated: May 24, 2026

Traction Force Microscopy to Study B Lymphocyte Activation
09:28

Traction Force Microscopy to Study B Lymphocyte Activation

Published on: July 23, 2020

Mechanosensing in T lymphocyte activation.

Edward Judokusumo1, Erdem Tabdanov, Sudha Kumari

  • 1Department of Biomedical Engineering, Columbia University, New York, New York, USA.

Biophysical Journal
|February 21, 2012
PubMed
Summary

T cells can sense mechanical forces, with activation increasing on stiffer surfaces. This mechanosensing is primarily linked to CD3 signaling, occurring downstream of T-cell receptor activation.

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Last Updated: May 24, 2026

Traction Force Microscopy to Study B Lymphocyte Activation
09:28

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Published on: July 23, 2020

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07:48

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist

Published on: April 25, 2018

Area of Science:

  • Cellular Mechanobiology
  • Immunology
  • Biophysics

Background:

  • Mechanical forces significantly influence cell behavior and function.
  • T cell activation is crucial for adaptive immunity.
  • Understanding how T cells interact with their physical environment is key.

Purpose of the Study:

  • To investigate T cell mechanosensing capabilities.
  • To determine the role of substrate stiffness in T cell activation.
  • To elucidate the signaling pathways involved in T cell mechanotransduction.

Main Methods:

  • Utilized polyacrylamide gels with varying elastic moduli (10-200 kPa) presenting CD3 and CD28 ligands.
  • Measured T cell activation via attachment and Interleukin-2 (IL-2) secretion.
  • Employed phospho-specific staining for Zap70 and Src family kinases.

Main Results:

  • Naive CD4 T cells showed enhanced activation (attachment, IL-2 secretion) with increasing substrate stiffness.
  • Mechanosensing was more pronounced with CD3 signaling compared to CD28 signaling.
  • Evidence suggests mechanosensing occurs downstream of T-cell receptor activation, involving Zap70 and Src family kinases.

Conclusions:

  • T cells possess a quantitative ability to sense and respond to substrate rigidity.
  • This finding offers a novel perspective on T cell mechanobiology and immune responses.
  • The study highlights the importance of the physical microenvironment in T cell function.