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. 2020 May 23;10(3):581–599. doi: 10.1016/j.jcmgh.2020.05.004

Figure 2.

Figure 2

CreERT model labels healthy adult Gli1-expressing fibroblasts. (A) Genetic scheme for Gli1CreERT/+ crossed with either a Rosa26YFP/+ or a Rosa26tdTomato/+ reporter. (B) Experimental design for examining healthy adult mice expressing Gli1 in the pancreas. Adult mice ages 5–8 weeks were given tamoxifen gavages (4 mg/mouse/day) for 5 days. Tissue was examined 1 week after completing gavages. (C) IHC staining for YFP in healthy adult mice. Scale bar: 50 um. (D) IF staining of the following: Lyve-1 (green), Tomato (red), and DAPI (blue); NG2 (green), Tomato (red), and DAPI (blue); PDGFRβ (green), Tomato (red), and DAPI (blue); and αSMA (green), Tomato (red), and DAPI (blue) in Gli1CreERT/+;RTom samples. Scale bar: 50 um. (E) Genetic scheme for a Gli1CreER/+;Gli1EGFP/+,RTomato mouse model. (F) IF staining of GFP and Tomato in the Gli1CreERT/+;Gli1EGFP/+;RTom mouse. Scale bar: 50 um. (G) Representative YFP vs PDGFR⍺, flow cytometry plots of DAPI- cells in a healthy Gli1CreERT/+;RYFP mouse and wild-type control and the quantification (n ≥ 10). (H) Representative YFP vs CD45 flow cytometry plot. (I) Quantification of the percentage of YFP+ cells that expressed CD45, PDGFR⍺, or CD105, as determined by flow cytometry gating. All data are expressed as means ± SEM. TAM, tamoxifen; TOM, Tomato; WT, wild-type.