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. 2021 Apr 1;28(4):637–652.e8. doi: 10.1016/j.stem.2020.11.004

Figure 1.

Figure 1

Identification of eight distinct non-hematopoietic cell populations

(A) HSPCs transduced with either thrombopoietin (ThPO) cDNA or control cDNA (EV) were transplanted (tx) at 0 weeks; n = 4 mice per time point and condition. Endpoint: 5 weeks (pre-fibrosis) and 10 weeks (fibrosis). Representative HE and reticulin staining. Scale bar, 50 μm.

(B) Hemoglobin (Hb) and platelet counts over time (mean ± SEM). Two-way-ANOVA with post hoc pairwise t test was used.

(C) UMAP of the non-hematopoietic BM niche identified by unsupervised clustering (n = 2,294 cells).

(D) Average gene expression of top marker genes within major cell populations (left panel). Feature plot of top markers in UMAP (right panel) is shown. Wilcoxon rank-sum test, p < 0.01). A full list of marker genes and corresponding GO terms is in Table S2.

(E) Heatmap of different MSC marker genes. Wilcoxon rank-sum test, p < 0.01.

(F) Venn diagram of the four identified MSC populations. Shared markers are highlighted in intersections.

(G) Heatmap SCP marker genes. Wilcoxon rank-sum test, p < 0.01.

See also Figure S1 and Tables S1 and S2.