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. 2022 Jan 7;12:797747. doi: 10.3389/fgene.2021.797747

FIGURE 1.

FIGURE 1

The cellular composition of dermal fibroblasts changes upon aging. (A) Experimental design. (B) Uniform Manifold Approximation and Projection (UMAP) plots of fibroblasts of young and old participants. (C) Expression of reticular (WISP2, SLPI, CTHRC1, MFAP5, TSPAN8), papillary (APCDD1, ID1, WIF1, COL18A1, PTGDS), pro-inflammatory (CCL19, APOE, CXCL2, CXCL3, EFEMP1) and mesenchymal (ASPN, POSTN, GPC3, TNN, SFRP1) markers (Solé-Boldo et al., 2020) among fibroblasts in UMAP plots. (D) Box plot of percentages of cells in fibroblast populations young vs. old, **** p<0.0001 (Fisher’s exact test). (E) Marker expression in UMAP plots, subclustering of population 4 into 4a and 4b. (F) Box plot of percentages of cells in fibroblast populations 4a and 4b young, vs. old, **** p<0.0001 (Fisher's exact test). F1-F4b Fibroblast populations 1–4b, yr years, y young, o old.