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. 2021 Mar 8;12:617564. doi: 10.3389/fimmu.2021.617564

Table 4.

Experimental conditions of live imaging of microglia in vitro.

Animal Age Isolation method Region Other cell type in the culture Cellular visualization Microscopy Objective lens Resolution (x, y)
z stack
Interval time
Total time
References
SOD1-G93A mice (animal model of myotrophic lateral sclerosis) 4 mo Density gradient centrifugation Whole brain Motor neuron Red (microglia)
GFP (motor neuron)
Confocal Frakes et al. (89)
C57BL/6 mice P3 Mild trypsinization of mix glial coculture Cortex Bacteria DIC Epifluorescence 10x or 20x Hupp et al. (90)
mice or rats P1-2 Shaking of mix glial coculture Cortex Neuron IsolectinB4-594 (microglia)
YFP (neuron)
Kraft et al. (91)
iPSCs Differentiation Synaptosome DIC (microglia)
pHrodo (synapptosome)
Confocal 0.61 × 0.61 μm
Sellgren et al. (92)

iPSCs, induced Pluripotent Stem Cells; P, post-natal day; mo, month-old; –, not available.