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. Author manuscript; available in PMC: 2021 Sep 3.
Published in final edited form as: Cell Stem Cell. 2020 Jul 27;27(3):413–429.e4. doi: 10.1016/j.stem.2020.06.019

Figure 1. Canonical Wnt/β-catenin signaling is essential for proximal ABSC proliferation after injury in vivo.

Figure 1.

A. Experimental schematic outlining intratracheal (i.t.) administration of polidocanol to wild type 6–10-week-old mice and euthanasia timeline post-injury.

B. qRT-PCR assessing mRNA expression levels of several components and targets of the Wnt/β-catenin signaling pathway from stripped tracheal epithelia of mice at varying timepoints post-polidocanol injury.

C. Images of in situ hybridization in uninjured and 48hpi wildtype mouse tracheas using probes targeting Axin2 mRNA.

D. IF images of p-β-cateninY489 (red) in uninjured and repairing mouse tracheal epithelia at varying timepoints post-injury.

E. IF images of TCF/Lef:H2B/GFP reporter mice with and without polidocanol injury.

F. Quantification of percentage of K5+ GFP+ cells in the surface airway epithelium of TCF/Lef:H2B/GFP reporter mice with and without polidocanol injury.

G. Experimental schematic outlining tamoxifen administration, i.t. polidocanol injury, BrdU administration, and euthanasia of Ctnnb1fl/fl and K5-CreER;Ctnnb1fl/fl transgenic mice.

H. IF images of uninjured and 48hpi mouse airway epithelia of Ctnnb1fl/fl and K5-CreER;Ctnnb1fl/fl transgenic mice assessing BrdU incorporation. Bottom images of a given timepoint are magnifications of outlined white box in top images.

Bar graph represents SEM, n = 3–6. *p < 0.05, *** p < 0.001 by Student’s t test.