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. 2019 May 23;51(5):1–16. doi: 10.1038/s12276-019-0247-x

Fig. 2. Effects of the Wnt and FGF signaling pathways on proliferation and differentiation during initial neuromast development.

Fig. 2

a1D3: Proliferative cells labeled with BrdU (red), SCs labeled with Sox2 (white), and HCs labeled with GFP (green). a1A3: Control neuromast; b1B3: After addition of BIO; c1C3: After addition of SU5402; d1D3: After 6 h of incubation with BIO, SU5402 and BIO were added for 18 h; e: Quantification of the proliferative cells (BrdU+), SCs (Sox2+), and HCs (GFP+) shown in a1D3. f1I3: Proliferative cells labeled with BrdU (red), SCs labeled with Sox2 (white), and HCs labeled with myosin VI (green). f1F3: wt Apc larvae; g1G3: Apcmcr mutants; h1H3: After addition of SU5402; i1I3: 54 hpf Apcmcr embryos were treated with SU5402 for 18 h. j: Quantification of the proliferative cells (BrdU+), SCs (Sox2+), and HCs (Myosin VI+) shown in f1I3. n = 5–7 fish per group. ** Indicates p < 0.001, # indicates p < 0.05, and error bars indicate the standard error of the mean. K1N1 and K2N2: WISH analysis of Sox2 (K1N1) and atoh1a (K2N2) expression in the neuromasts from different groups. Scale bar in I3 = 20 μm for a1D3 and f1I3. Scale bar in N2 = 30 μm for K1N1, K2N2