A subscription to JoVE is required to view this content. Sign in or start your free trial.

Method Article

Utilizing Bead-Supported Lipid Bilayers to Investigate the Synaptic Output from T Cells

686 views

July 8th, 2025

In This Article

Abstract

Source: Céspedes, P. F., et al. Preparation of Bead-supported Lipid Bilayers to Study the Particulate Output of T Cell Immune Synapses. J. Vis. Exp. (2022)

This video illustrates the reconstitution of synthetic antigen-presenting cells through Bead-Supported Lipid Bilayers and their application in assessing the synaptic output generated by activated T cells.

Protocol

1. Protein density calibrations on BSLBs (Bead-supported lipid bilayers)

  1. Before taking the 5.00 ±0.05 µm diameter non-functionalized silica beads, mix the stock solution well and resuspend any big clumps of beads sedimented on the bottom of the flasks.
    NOTE: Silica beads tend to sediment quickly, which might lead to counting errors. Mix vigorously by pipetting up and down half of the maximum volume of a P1000 micropipette.
  2. Dilute 1 µL of bead solution in 1,000 µL of PBS, count the beads using a hemocytometer chamber, and calculate their concentration per mL.
    NOTE:

Access restricted. Please log in or start a trial to view this content.

Results

Flow cytometry data analysis showing ICAM-1 expression; includes various gating strategies, graph.
Figure 1: Absolute quantification of proteins on the surface of APCs. (A) Example of quantitative flow cytometry measurements of ICAM-1 on the surface of tonsillar B cells (Foll. Bc) and helper T cells (TFH). (i-vii) Gati.......

Access restricted. Please log in or start a trial to view this content.

Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
96 Well Cell Cultture Plate U-bottom with Lid, Tissue culture treated, nonpyrogenicCostar®3799For FCM staining and co-culture of BSLB and cells.
96 Well Cell Cultture Plate V-bottom with Lid, Tissue culture treated, nonpyrogenic.Costar®3894For FCM staining of cells or beads in suspension.
Alexa Fluor 488 NHS Ester (Succinimidyl Ester)Thermo Fisher Scientific, Invitrogen™A20000
Alexa Fluor 647 NHS Ester (Succinimidyl Ester)Thermo Fisher Scientific, Invitrogen™A37573 and A20006
Multiwell 6 well Tissue culture treated with vacuum gas plasmaFalcon353046For culturing and expanding purified CD4+ and CD8+ T cells.
Casein from bovine milk, suitable for substrate for protein kinase (after dephosphorylation), purified powder
Dynabeads Human T-Activator CD3/ CD28ThermoFisher Scientific, Gibco11132D
DynaMag-2ThermoFisher Scientific, Invitrogen™12321DFor the removal of Dynabeads Human T-Activator CD3/CD28 in volumes less than 2 mL
DynaMag™-15ThermoFisher Scientific, Invitrogen™12301DFor the removal of Dynabeads™ Human T-Activator CD3/CD28 in volumes less than 15 mL
Fetal Bovine Serum Qualified, One ShoThermoFisher Scientific, GibcoA3160801Needs heat inactivation for 30 min at 56 oC
anti-human CD154 (CD40L), clone 24-31BioLegend310815 and 310818Alexa Fluor 488 and Alexa Fluor 647 conjugates, respectively
Armenian Hamster IgG Alexa Fluor 647 Isotype control, clone HTK888BioLegend400902Labelled in house with Alexa Fluor 647 NHS Ester (Succinimidyl Ester)
BD Cytometer Setup and Tracking beadsBecton Dickinson & Company (BD)641319Performance track of instruments before quantitative FCM

Tags

T Cell Immune SynapseFlow Cytometry AnalysisAntigenic Peptide-MHCCo-Stimulatory MoleculesTrans-Synaptic VesiclesCentrifugation ProtocolFluorescent Antibody StainingSynthetic Antigen-Presenting CellsImmune Synapse Formation