Composition and structure of synaptic ectosomes exporting antigen receptor linked to functional CD40 ligand from helper T cells

Author:

Saliba David G12ORCID,Céspedes-Donoso Pablo F1ORCID,Bálint Štefan1ORCID,Compeer Ewoud B1ORCID,Korobchevskaya Kseniya1,Valvo Salvatore1,Mayya Viveka1,Kvalvaag Audun1,Peng Yanchun34,Dong Tao34ORCID,Tognoli Maria-Laura5,O'Neill Eric5,Bonham Sarah6,Fischer Roman6ORCID,Kessler Benedikt M6,Dustin Michael L1ORCID

Affiliation:

1. Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom

2. Department of Applied Biomedical Science, Faculty of Health Science, University of Malta, Msida, Malta

3. MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom

4. Nuffield Department of Medicine, Chinese Academy of Medical Science Oxford Institute, University of Oxford, Oxford, United Kingdom

5. Department of Oncology, University of Oxford, Oxford, United Kingdom

6. Discovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom

Abstract

Planar supported lipid bilayers (PSLB) presenting T cell receptor (TCR) ligands and ICAM-1 induce budding of extracellular microvesicles enriched in functional TCR, defined here as synaptic ectosomes (SE), from helper T cells. SE bind peptide-MHC directly exporting TCR into the synaptic cleft, but incorporation of other effectors is unknown. Here, we utilized bead supported lipid bilayers (BSLB) to capture SE from single immunological synapses (IS), determined SE composition by immunofluorescence flow cytometry and enriched SE for proteomic analysis by particle sorting. We demonstrate selective enrichment of CD40L and ICOS in SE in response to addition of CD40 and ICOSL, respectively, to SLB presenting TCR ligands and ICAM-1. SE are enriched in tetraspanins, BST-2, TCR signaling and ESCRT proteins. Super-resolution microscopy demonstrated that CD40L is present in microclusters within CD81 defined SE that are spatially segregated from TCR/ICOS/BST-2. CD40L+ SE retain the capacity to induce dendritic cell maturation and cytokine production.

Funder

European Commission

Wellcome

Cancer Research UK

Chinese Academy of Sciences

National Institutes of Health

Kennedy Trust for Rheumatology Research

European Molecular Biology Organization

Research Council of Norway

H2020 Marie Skłodowska-Curie Actions

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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