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. Author manuscript; available in PMC: 2022 Mar 9.
Published in final edited form as: Nature. 2021 Oct 27;599(7886):667–672. doi: 10.1038/s41586-021-04044-7

Fig. 2 |. neoTreg cell reduction causes outgrowth of an Il13ra1+ fibroblast population in skin fascia.

Fig. 2 |

ad, scRNA-seq of Lin stromal cells (EpCAMCD31CD45) sorted from skin of control and ΔneoTreg mice at P22. Il13ra1+ fibroblast (FB) clusters are circled. n = 2 animals pooled per group. prolif, proliferative. a, Unsupervised clustering. b, Relative cluster abundance in ΔneoTreg skin. Arrows indicate Il13ra1+ FB clusters. c, Gene expression by cluster in control sample. d, Gating strategy for Il13ra1+ fibroblasts in P25 control skin. The top plot shows total live cells. e, f, Expression of selected Il13ra1+ FB markers identified by scRNA-seq (e) was measured by quantitative PCR of sorted cells (f) to validate the gating strategy in d (bulk SCA1+: CD34+ SCA1+CD26+/−CD9+; other stroma: CD34SCA1; f). n = 4 animals. g, Localization of Il13ra1+ fibroblasts stained for CD26 in back skin of P25 mice. Scale bar, 50 μm. h, Flow cytometry quantification of Il13ra1+ fibroblasts at P22. n = 12 animals. Data are displayed as the mean ± s.d. from one independent experiment, representative of one (ac, e) or two-to-three repeats (d, fh). *P < 0.05, **P < 0.01 (all two-sided); repeated measures ANOVA with Geisser–Greenhouse correction and Dunnett’s multiple comparisons test (f) or Student’s t-test (h).