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. Author manuscript; available in PMC: 2018 Sep 7.
Published in final edited form as: Cell. 2017 Sep 7;170(6):1134–1148.e10. doi: 10.1016/j.cell.2017.07.034

Figure 1. Signaling pathway reporter activity identified distinct mesenchymal cells in the adult mouse lung.

Figure 1

(A–D) Axin2CreERT2:tdT reporter mice express tdTomato throughout the lung mesenchyme. (E–H) Axin2-lineage traced cells shows that Axin2+ positive cells surrounding the airways rarely express Pdgfrα (E, black arrowhead) whereas they do express Pdgfrβ+ (F, white arrowhead). In contrast, Axin2+ cells in the alveolar region are predominantly Pdgfrα positive (E and G, white arrowheads) and generally do not express Pdgfrβ (H, black arrowhead). (I) Wnt2-expressing mesenchymal cells are only present in the alveolar compartment. (J and K) Immunostaining shows that Wnt2-derived cells are Pdgfrα+ (white arrowhead) and not Pdgfrβ+ (black arrowhead). (L) Wnt2creERT2:R26RtdTomato:PdgfrαEGFP mice reveal that the majority of Wnt2+ cells are PdgfrαEGFP positive. (M) Axin2CreERT2:tdT:PdgfrαEGFP mice reveal Axin2-Pα double positive and Axin2-tdT single positive cells, with the Axin2-Pα cells found primarily in the alveolar region (inset). (N) Quantification of the spatial distribution of Axin2 and PdgfrαEGFP positive cells (left graph) and quantification of the alveolar distribution of Wnt2 mesenchymal cells (right graph). (O) Schematic showing the mesenchymal populations and their general spatial distributions. Data in N are means ± SEM. Scale bars A–K low magnification are 50 µm, high magnification are 10 µm. aw=airway, v=blood vessel, asm= airway smooth muscle, pbm= peri-bronchial mesenchyme and epi=epithelium.