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. 2024 Dec 20;22:1114. doi: 10.1186/s12967-024-05869-2

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Fig. 6 — The mRNA expression of 4 selected genes in IPF at single cell level. UMAP plots showing the distribution of classical subpopulations of epithelial cells (A), immune cell (C) and stromal cells (E). Dot plots showing the expression of marker genes corresponding to epithelial cell subpopulations (B), immune cell subpopulations (D) and stromal cell subpopulations (E). The mRNA expression of 4 selected genes in epithelial cell subpopulations (G), immune cell subpopulations (H) and stromal cell subpopulations (I). The expression of ANGPTL4 in PMCs (J). MMT is activated in PMCs of IPF when compared with healthy control (K)