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Updated: Nov 19, 2025

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion STED Microscopy
Published on: April 9, 2018
Dendritic cell actin dynamics control contact duration and priming efficiency at the immunological synapse
Alexander Leithner1,2, Lukas M Altenburger3, Robert Hauschild1
1Institute of Science and Technology Austria, Klosterneuburg, Austria.
Insights
Dendritic cells
Area of Science:
- Immunology
- Cell Biology
- Cytoskeletal Dynamics
Background:
- Dendritic cells (DCs) initiate adaptive immunity by priming naive T cells at the immunological synapse (IS).
- F-actin dynamics on the T cell side of the IS are well-studied, but the DC cytoskeletal role remains unclear.
Purpose of the Study:
- To investigate the contribution of the dendritic cell actin cytoskeleton to immunological synapse formation and T cell priming.
Main Methods:
- Utilized microscopy to observe DC actin dynamics at the IS.
- Investigated the role of the WAVE regulatory complex (WRC) in DC cytoskeletal regulation.
- Assessed T cell activation and proliferation following interaction with DCs lacking WRC.
Main Results:
- DC actin cytoskeleton forms a multifocal synaptic structure crucial for T cell priming efficiency.
- DC actin at the IS appears in transient foci regulated by the WAVE regulatory complex (WRC).
- Absence of WRC in DCs leads to stabilized cell-cell contacts and reduced T cell activation and proliferation.
Conclusions:
- The dendritic cell actin cytoskeleton, regulated by the WRC, is essential for dynamic IS formation.
- DC cytoskeletal dynamics directly impact T cell priming efficiency by modulating cell-cell adhesion and synapse stability.
Abstract:
Dendritic cells (DCs) are crucial for the priming of naive T cells and the initiation of adaptive immunity. Priming is initiated at a heterologous cell-cell contact, the immunological synapse (IS). While it is established that F-actin dynamics regulates signaling at the T cell side of the contact, little is known about the cytoskeletal contribution on the DC side. Here, we show that the DC actin cytoskeleton is decisive for the formation of a multifocal synaptic structure, which correlates with T cell priming efficiency. DC actin at the IS appears in transient foci that are dynamized by the WAVE regulatory complex (WRC). The absence of the WRC in DCs leads to stabilized contacts with T cells, caused by an increase in ICAM1-integrin-mediated cell-cell adhesion. This results in lower numbers of activated and proliferating T cells, demonstrating an important role for DC actin in the regulation of immune synapse functionality.
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