This video demonstrates a high-resolution total internal reflection fluorescence (TIRF) microscopy technique for real-time visualization of phagosome formation and closure during macrophage-mediated phagocytosis of IgG-opsonized red blood cells (RBCs) attached to the surface of a glass bottom dish. The macrophages extend pseudopodia around the RBCs and engulf them inside the phagosomes, detaching them from the glass surface.
Protocol
All procedures involving sample collection have been performed in accordance with the institute's IRB guidelines. Note: The plasmid used Lifeact-mCherry is a kind gift of Dr. Guillaume Montagnac, Institut Curie, Paris. 1. Cells and Transfection Note: RAW264.7 macrophages are grown to subconfluency in complete medium (RPMI (Roswell Park Memorial Institute) 1640 medium, 1…
Representative Results
Figure 1. Schematic Representation of the "Phagosome Closure Assay" Analyzed by TIRFM. The phagosome closure assay is performed using macrophages transiently expressing one or two fluorescently tagged protein. Macrophages are deposited on IgG-opsonized SRBCs non-covalently fixed on poly-lysine coated coverslips. Images are recorded in TIRF mode to detect the site of phagosome closure and …
Divulgations
The authors have nothing to disclose.
Materials
Anti-sheep red blood cells IgG
MP Biomedicals
55806
Bovine Serum Albumin heat shock fraction, pH 7, ≥98%
Sigma
A7906
Cell lifter
Corning
3008
Cuvettes 4mm
Cell project
EP104
DPBS, no calcium, no magnesium
Thermo Fischer Scientific
14190-094
Room temperature
Electrobuffer kit
Cell project
EB110
100mm TC-Treated Cell Culture Dish
Corning
353003
Gene X-cell pulser
Biorad
165-2661
Gentamicin solution
Sigma
G1397
Glass Bottom Dishes 35 mm uncoated 1.5
MatTek corporation
P35G-1.5-14-C Case
iMIC
TILL Photonics
Oil-immersion objective (N 100x, NA1.49.), heating chamber with CO2, a camera single photon detection EMCCD ( Electron Multiplying Charge Coupled Device) and a 1.5X lens