WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts

<p style="text-align:justify;"> The immunological synapse is a highly structured and molecularly dynamic interface between communicating immune cells. Although the immunological synapse promotes T cell activation by dendritic cells, the specific organization of the immunological syn...

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Huvudupphovsmän: Malinova, D, Fritzsche, M, Nowosad, C, Armer, H, Munro, P, Blundell, M, Charras, G, Tolar, P, Bouma, G, Thrasher, A
Materialtyp: Journal article
Publicerad: Wiley 2015
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author Malinova, D
Fritzsche, M
Nowosad, C
Armer, H
Munro, P
Blundell, M
Charras, G
Tolar, P
Bouma, G
Thrasher, A
author_facet Malinova, D
Fritzsche, M
Nowosad, C
Armer, H
Munro, P
Blundell, M
Charras, G
Tolar, P
Bouma, G
Thrasher, A
author_sort Malinova, D
collection OXFORD
description <p style="text-align:justify;"> The immunological synapse is a highly structured and molecularly dynamic interface between communicating immune cells. Although the immunological synapse promotes T cell activation by dendritic cells, the specific organization of the immunological synapse on the dendritic cell side in response to T cell engagement is largely unknown. In this study, confocal and electron microscopy techniques were used to investigate the role of dendritic cell actin regulation in immunological synapse formation, stabilization, and function. In the dendritic cell‐restricted absence of the Wiskott‐Aldrich syndrome protein, an important regulator of the actin cytoskeleton in hematopoietic cells, the immunological synapse contact with T cells occupied a significantly reduced surface area. At a molecular level, the actin network localized to the immunological synapse exhibited reduced stability, in particular, of the actin‐related protein‐2/3‐dependent, short‐filament network. This was associated with decreased polarization of dendritic cell‐associated ICAM‐1 and MHC class II, which was partially dependent on Wiskott‐Aldrich syndrome protein phosphorylation. With the use of supported planar lipid bilayers incorporating anti‐ICAM‐1 and anti‐MHC class II antibodies, the dendritic cell actin cytoskeleton organized into recognizable synaptic structures but interestingly, formed Wiskott‐Aldrich syndrome protein‐dependent podosomes within this area. These findings demonstrate that intrinsic dendritic cell cytoskeletal remodeling is a key regulatory component of normal immunological synapse formation, likely through consolidation of adhesive interaction and modulation of immunological synapse stability. </p>
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spelling oxford-uuid:988fa1f1-4dff-408f-ad8f-27e3e9487e2e2022-03-27T00:07:51ZWASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contactsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:988fa1f1-4dff-408f-ad8f-27e3e9487e2eSymplectic Elements at OxfordWiley2015Malinova, DFritzsche, MNowosad, CArmer, HMunro, PBlundell, MCharras, GTolar, PBouma, GThrasher, A <p style="text-align:justify;"> The immunological synapse is a highly structured and molecularly dynamic interface between communicating immune cells. Although the immunological synapse promotes T cell activation by dendritic cells, the specific organization of the immunological synapse on the dendritic cell side in response to T cell engagement is largely unknown. In this study, confocal and electron microscopy techniques were used to investigate the role of dendritic cell actin regulation in immunological synapse formation, stabilization, and function. In the dendritic cell‐restricted absence of the Wiskott‐Aldrich syndrome protein, an important regulator of the actin cytoskeleton in hematopoietic cells, the immunological synapse contact with T cells occupied a significantly reduced surface area. At a molecular level, the actin network localized to the immunological synapse exhibited reduced stability, in particular, of the actin‐related protein‐2/3‐dependent, short‐filament network. This was associated with decreased polarization of dendritic cell‐associated ICAM‐1 and MHC class II, which was partially dependent on Wiskott‐Aldrich syndrome protein phosphorylation. With the use of supported planar lipid bilayers incorporating anti‐ICAM‐1 and anti‐MHC class II antibodies, the dendritic cell actin cytoskeleton organized into recognizable synaptic structures but interestingly, formed Wiskott‐Aldrich syndrome protein‐dependent podosomes within this area. These findings demonstrate that intrinsic dendritic cell cytoskeletal remodeling is a key regulatory component of normal immunological synapse formation, likely through consolidation of adhesive interaction and modulation of immunological synapse stability. </p>
spellingShingle Malinova, D
Fritzsche, M
Nowosad, C
Armer, H
Munro, P
Blundell, M
Charras, G
Tolar, P
Bouma, G
Thrasher, A
WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title_full WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title_fullStr WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title_full_unstemmed WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title_short WASp‐dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive, functional T cell contacts
title_sort wasp dependent actin cytoskeleton stability at the dendritic cell immunological synapse is required for extensive functional t cell contacts
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