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. 2022 Oct 14;13:6078. doi: 10.1038/s41467-022-33458-8

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — A FACS analysis of MERTK, CD64, CD14 and HLA-DR cell surface expression on monocytes or monocyte-derived macrophages. The control (green curve) corresponds to macrophages differentiated with human serum. B, C Expression of macrophage markers CD206, IL1-ra, TNF, and IL-1B in macrophages incubated with CM from A549 or A549 + fibrocytes co-cultures, n = 6. D Migration (n = 3 independent experiments, 3 technical replicates) and (E) proliferation (n = 3 independent experiments, 8 technical replicates) of macrophages incubated with CM from A549 or fibrocytes or A549 + fibrocyte co-cultures. E ET₁, ET_A and ET_B mRNA expression in A549 or A549 + fibrocyte coculture, n = 6. G Endothelin levels of A549 or fibrocytes or A549 + fibrocytes CM, n = 3. B–E, G P-values were determined using One-way ANOVA with Fisher’s LSD test. F P-values were determined using two-tailed unpaired t-test with Welsh’s correction. Source data are provided in the source data file.