Antigen, co-stimulation, co-repression, adhesion molecules and viral proteins are loaded on the surface of BSLB to generate tailored, synthetic antigen presenting cells. By providing these signals, BSLB instigate synapse formation and the release of patches of SV containing a variety of effectors, including CD40L, Perforin, ectonucleotidases, tetraspanins and small RNA species. Using CD40L as a model helper T cell effector we then explored the dynamics influencing the release of CD40L+ SV, and demonstrate the role of T cell phenotypes, antigen and CD40 density, antigen potency, co-stimulation, co-repression, enzymatic processing by ADAM10 and the facilitating role of structural proteins including bone marrow stromal cell Bone Marrow Stromal Cell Antigen 2 (BST2, CD317) and CD81. Altogether, we demonstrate the broad applicability of BSLB for the dissection of T cell effectors delivered in the form of synaptic vesicles born either from the plasma membrane or intracellular stores.
Professor of Immunology and Wellcome Principal Research Fellow, Director of Research of the Kennedy Institute:
Prof. Michael Dustin has a B.A. in Biology from Boston University (1984) and a Ph.D. in Cell and Developmental Biology from Harvard University (1990). His lab at Washington University led pioneering work on the immunological synapse in the 1990’s. Work at NYU School of medicine in the 2000’s explored in vivo dynamics of the immune response using two-photon laser scanning microscopy. Work over the last decade explored the nanoscale organization of the immunological synapse leading to a basic description of the supramolecular assemblies that make up the mature immunological synapse. This includes synaptic ectosomes and supramolecular attack particles (see publication links below). He moved his lab to the University of Oxford in 2013 supported by a Principal Research Fellowship from Wellcome and the Kennedy Trust for Rheumatology Research.
Dustin, M Group | Immunological synapse Research Group, Kennedy Institute