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. Author manuscript; available in PMC: 2021 Dec 3.
Published in final edited form as: Dev Dyn. 2021 Jun 16;250(12):1778–1795. doi: 10.1002/dvdy.383

Figure 9: Muscle-specific knockout of Fgf9 in mice (Fgf9cKO) resulted in larger superstructures and increased number of acetylcholine receptor (AChR) clusters in the deltoid muscle.

Figure 9:

MicroCT scans of 8 week (A) WT and (E) Fgf9cKO mice show a significantly larger DT (DT;red) and lateral supracondylar ridge (LSR; yellow) in Fgf9cKO mice. Histology of the DT support this phenotype (B, F). Skeletal muscle specificity of Acta1-Cre was confirmed using Ai14 reporters (H,G). Gene expression of (I) Agrn (p = 0.0287) and (J) Ikbkb (p = 0.0675) were increased in Fgf9cKO deltoid muscle compared to WT muscle at 8 weeks of age (ΔCT calculated using average reference gene CT of ipo8 and Rn18s). Immunofluorescence (IF) was used to visualize nerves (neurofilament, green) and AChR clusters at neuromuscular junctions (α-bungarotoxin, red) in (K) WT and (L) Fgf9cKO mice. At 3 weeks postnatally, Fgf9cKO mice had significantly higher (N) AchR density than WT littermates and (M) more AChR. Data shown are biological replicates, mean ± SD. Lines in C, D, I, and N indicate significance (p < 0.05).