APC is required for adult skeletal muscle regeneration. (A) TM regimen and cardiotoxin (CTX) injury scheme for control and APC SC-KO mice. (B and C) Immunostaining for Pax7 (B) and e-MyHC (C) on TA cryosections 4 d after injury. (D–L) Analysis of TA muscles 14 d after injury reveals that tissue regeneration is defective in APC SC-KO muscles. (D) Whole sections of TA muscles immunostained for Laminin. Immunostaining for Tcf4 (F), type 1 Collagen (H), and Pax7 and Laminin (L) on TA cryosections is shown. Quantification of TA weight 14 d after injury normalized by uninjured TA weight (E), of the number of Tcf4+ cells/mm2 (G), of relative Collagen+ area (I), and of sublaminar Pax7+ cells (normalized by Pax7+ cells of uninjured TA; J) is also shown. (K) GFP immunostaining on transverse sections of TAs isolated from Pax7CreER;Z/EG (Control-Z/EG) and Pax7CreERAPClox/lox;Z/EG (APC SC-KO-Z/EG) 14 d after injury demonstrates that APC-null satellite cells do not give rise to new myofibers, nor trans-differentiate in other cell types. Bars: (B, C, F, H, K, and L) 50 µm; (D) 200 µm. Nuclei are stained with Hoechst. Error bars indicate SEM. Inset panels show a 2× enlargement.