ZFIN Image: Serrano et al., 2021, Fig. 3.

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Figure Caption

Fig. 3.

Assessment of neuronal pathology in cdkl5^−/− fish. (A) Maximum intensity projection confocal images of EGFP-labelled motor neurons from Tg(islet1:EGFP); cdkl5^+/+ (white dashed box zoomed in i) and Tg(islet1:EGFP); cdkl5^−/− (white dashed box zoomed in ii) along the spinal region at 6 dpf. Red dashed boxes indicate the regions quantified in C. Scale bars: 50 µm. (B) Quantification of the number of EGFP⁺ motor neurons at 6 dpf. Data are mean±95% c.i. for three independent experiments [n=8, 8 and 8 for Tg(islet1:EGFP); cdkl5^+/+, and n=8, 8 and 8 for Tg(islet1:EGFP); cdkl5^−/− fish]. (C) Quantification of the mean percentage area of fluorescence from Tg(islet1:EGFP); cdkl5^+/+ and Tg(islet1:EGFP); cdkl5^−/− (within the red dashed box region in A) at 6 dpf. Data are mean±s.e.m. for three independent experiments [n=8, 8 and 8 for Tg(islet1:EGFP); cdkl5^+/+, and n=8, 8 and 8 for Tg(islet1: EGFP); cdkl5^−/− fish]. **P<0.01; NS, not significant (two-tailed t-test).

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Acknowledgments

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