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Related Concept Videos

Cell Polarization by Rho Proteins01:21

Cell Polarization by Rho Proteins

Cell polarity is the asymmetric distribution of cellular and membrane components, making one side of the cell different from the other. This polarity is essential to many processes such as embryogenesis, axon migration, glucose transport across epithelial cells, and directional cell migration. A migrating cell responds to intracellular or extracellular signals via molecular cascades that reorganize the actin cytoskeleton to establish this polarity. In these cells, the Rho family proteins Cdc42,...
Small GTPases - Ras and Rho01:24

Small GTPases - Ras and Rho

Ras and Rho are small monomeric GTPases that act downstream of receptor tyrosine kinase (RTK) and regulate various cellular processes. These GTPases switch between active and inactive states by binding to guanine nucleotides.
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T Cell Types and Functions01:24

T Cell Types and Functions

When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
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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.
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Cytoskeletal Coordination in Cell Migration01:32

Cytoskeletal Coordination in Cell Migration

A migrating cell changes its shape during the cyclic events of attachment and detachment from the substratum and repositions the cell organelles correspondingly. These complex events are orchestrated by the dynamic cytoskeletal network comprising actin filaments, intermediate filaments, and microtubules. Cytoskeletal crosstalk — the direct and indirect communication between the different components — is crucial for this coordination. Direct communication involves various linker proteins that...
Role of Myosin in Cell Migration01:18

Role of Myosin in Cell Migration

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

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Published on: May 24, 2024

Multiple roles for RhoA during T cell transendothelial migration.

Sarah J Heasman1, Anne J Ridley

  • 1Randall Division of Cell and Molecular Biophysics; King's College London; London, UK.

Small Gtpases
|June 21, 2011
PubMed
Summary

The Rho GTPase RhoA is crucial for T-cell migration across endothelial barriers, regulating cell shape and movement. RhoA activity at the cell front and rear drives T-cell polarization, protrusion, and transmigration.

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Area of Science:

  • Immunology
  • Cell Biology
  • Biochemistry

Background:

  • T-cell migration across endothelial barriers is vital for immune surveillance and inflammatory responses.
  • This process involves T-cell adhesion, polarization, crawling, and transmigration, regulated by cytoskeletal dynamics.
  • Rho GTPases are key regulators of cell migration, controlling cytoskeletal organization and adhesion.

Purpose of the Study:

  • To investigate the role of the Rho GTPase RhoA in T-cell migration and transmigration across endothelial cells.
  • To determine the localization and activity of RhoA during T-cell crawling and transmigration.

Main Methods:

  • Depletion of RhoA in T cells.
  • Live imaging of T-cell migration on endothelial cells using a RhoA activity biosensor.
  • Analysis of T-cell morphology, polarization, and migratory behavior.

Main Results:

  • RhoA depletion impairs T-cell polarization, lamellipodia/uropod formation, and efficient migration on and through endothelial cells.
  • RhoA activity was detected in the lamellipodia, filopodia, and uropod of migrating and transmigrating T cells.
  • RhoA activity in lamellipodia correlated with both protrusion and retraction, suggesting dual roles.

Conclusions:

  • RhoA is essential for efficient T-cell polarization, migration, and transmigration.
  • RhoA signaling pathways, potentially involving mDIA1 for protrusion and ROCK for retraction, coordinate T-cell movement.
  • Specific guanine-nucleotide exchange factors (GEFs) likely orchestrate localized RhoA activation for distinct migratory functions.