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. 2016 Dec 19;11(12):e0167315. doi: 10.1371/journal.pone.0167315

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© 2016 Maisonnasse et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 2 — (A) The different subsets from BAL were sorted by flow cytometry. mRNA expression levels of 10 genes were assessed by RT-qPCR. For each gene, data were normalized to the reference gene RPS24 (Ribosomal Protein S24) expression and presented as relative expression (arbitrary units (AU)): for each animal, the population with the highest expression was considered as 100 and the other populations were normalized to it. Each symbol represents one animal. For the sake of an easier comparison between parenchymal (closed symbols) and BAL (open symbols) populations, parenchymal cells data (closed symbols), previously published in [2] were integrated in this figure. B) Heat map depicting the results from 2A. cDC = conventional Dendritic Cells, moDC = monocyte-derived DC, moMacro = monocyte-derived Macrophages, AM = alveolar Macrophages. Statistic signs *: P<0.01, **: P<0.001 with Student t-test.