Table 1.
Samples | Type of cells | Engulfed substrates | Techniques adopted | References |
---|---|---|---|---|
Cell lines | Microglia cell line BV-2 | Fluorescent beads | Fluorescent microscopy, Flow cytometry | (100) |
Microglial cell line MMGT12 |
Fluorescent beads | Flow cytometry | (101) | |
Microglial cell line BV-2 |
Synaptosomes | Fluorescent microscopy | (102) | |
iPC-derived microglia | Induced Microglia Like Cells (iMGL) |
Synaptosomes | Fluorescent microscopy | (103, 104) |
Primary cultures | Newborn microglia | Fluorescent beads and liposomes (DiO Labeled) |
Fluorescent microscopy | (21) |
fluorescent beads | Fluorescent microscopy, Flow cytometry | (20) | ||
Fluorescent bioparticles | Fluorescent microscopy | (105) | ||
Adult microglia | Ultraviolet-irradiated (UV-irr) dead neurons | Fluorescent microscopy | (78) | |
Fluorescent microspheres | Fluorescent microscopy | (62) | ||
Macrophages | Bacteria and cancer cells | CyTOF | (106) |
The table reports some commonly used experimental approaches to study microglial phagocytosis in vitro.