The Actin Cytoskeleton at the Immunological Synapse of Dendritic Cells.

Front Cell Dev Biol

Department of Cellular and Molecular Biology, Centro de Investigaciones Biológicas Margarita Salas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

Published: August 2021

AI Article Synopsis

  • Dendritic cells (DCs) are crucial for activating T cells (TCs) by forming an immunological synapse (IS) that facilitates communication between the two cell types.
  • The IS has two sides: IS(DC) representing dendritic cells and IS(TC) representing T cells, consisting of various proteins and cytoskeletal structures that help regulate T cell activation.
  • Research suggests that the actin cytoskeleton at the IS(DC) plays a critical role in stabilizing this interaction, which is vital for effectively activating T cells.

Article Abstract

Dendritic cells (DCs) are considered the most potent antigen-presenting cells. DCs control the activation of T cells (TCs) in the lymph nodes. This process involves forming a specialized superstructure at the DC-TC contact zone called the immunological synapse (IS). For the sake of clarity, we call IS(DC) and IS(TC) the DC and TC sides of the IS, respectively. The IS(DC) and IS(TC) seem to organize as multicentric signaling hubs consisting of surface proteins, including adhesion and costimulatory molecules, associated with cytoplasmic components, which comprise cytoskeletal proteins and signaling molecules. Most of the studies on the IS have focused on the IS(TC), and the information on the IS(DC) is still sparse. However, the data available suggest that both IS sides are involved in the control of TC activation. The IS(DC) may govern activities of DCs that confer them the ability to activate the TCs. One key component of the IS(DC) is the actin cytoskeleton. Herein, we discuss experimental data that support the concept that actin polarized at the IS(DC) is essential to maintaining IS stability necessary to induce TC activation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366227PMC
http://dx.doi.org/10.3389/fcell.2021.679500DOI Listing

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