This video demonstrates the in vitro study of immunological synapse formation between an antigen-presenting cell and helper T lymphocytes using a fluorescence microscope. T cell receptors of helper T lymphocytes interact with an antigen-MHC-II complex in antigen-presenting cells and form immunological synapses, followed by secretory vesicle movements toward the synapse, which is visualized by fluorescent microscopy.
Protocol
1. Preparation of Slides to Adhere Raji Cells Add 150 µL of fibronectin (100 µg/mL) per well to an 8 microwell chamber slide (plastic-bottom chamber slide) and incubate it for 30 min to 1 h at 37 °C. This adhesion substrate will allow the binding of Raji cells to the well bottom (Step 2), the formation of living conjugates with Jurkat cells (Step 4) cells, and time-lapse microscopy capture (step 6), and is also compatible afterward with optional paraformaldehyde (PFA) fixation….
Representative Results
Figure 1 represents synaptic Jurkat-Raji conjugates that were obtained following the protocol (step 5.2). The image represents the first frame from a representative, time-lapse experiment. 2 x 105 Raji cells and 2 x 105 Jurkat cells were added to a 1 cm2 well. The upper panel shows transmittance channel, the middle panel consists of CMAC (blue) chan…
Disclosures
The authors have nothing to disclose.
Materials
Camera Nikon DS-QI1MC
Nikon
MQA11550
Cooled Camera Head
CMAC
ThermoFisher Scientific
C2110
Cell tracker blue
JURKAT cells
ATCC
ATCC TIB-152
Effector T lymphocytes
μ-Slide 8 well ibiTreat, μ-Slide 8 well Glass-Bottom
IBIDI
Cat.No: 80826, 80827
Cell culture and cell imaging supports
Microscope NIKON Eclipse Ti-E
Nikon
NIKON Eclipse Ti-E
Wide-field fluorescence, fully-motorized microscope equipped with Perfect Focus System (PFS) option
Microscope Stage Incubator with 3-channel manual gas mixer and gas bubbler/ humidity module