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. 2022 May 25;39(11):110945. doi: 10.1016/j.celrep.2022.110945

Figure 5.

Figure 5

Lung-infiltrating monocytes release inflammatory mediators and harbor replicative SARS-CoV-2

(A) Inflammatory mediators in the apical fluid following transmigration were quantified by a multiplexed electrochemiluminescent assay. The Z score for each mediator in each condition was calculated and plotted.

(B) Transmigration efficiency of monocytes was calculated by dividing the number of monocytes in the apical fluid after 24 h by the input number of cells.

(C–E) RNA was extracted from each component of the model (epithelium, lung-infiltrating monocytes, and extracellular fluid) and reverse transcribed. Total SARS-CoV-2 genome copies were calculated.

(F) The sum of each of the components of the model was calculated to depict the total amount of virus remaining in the system after monocytes were allowed to transmigrate for 24 h.

All statistics were calculated using the Mann-Whitney U-test in Prism between the “no drug” and each treatment group. p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001. Shown are median and interquartile range.