Figure 2
- ID
- ZDB-FIG-200306-96
- Publication
- Coolen et al., 2020 - Mosaic Heterochrony in Neural Progenitors Sustains Accelerated Brain Growth and Neurogenesis in the Juvenile Killifish N. furzeri
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A Population of Apical Non-glial Progenitors Accounts for the Majority of Proliferating Progenitors in the Killifish Pallium (A) Immunostaining for GS (green), Sox2 (blue), and pH3 (magenta) at 8 dph. Shown is a dorsal 3D view. Shown in (A’) is high magnification of a 5 μm transverse section through the 3D reconstruction. Shown in (A″) is high magnification of a single optical z-plane. White arrows point to non-glial NGP progenitors entering mitosis at the apical surface and green arrows point to sparsely distributed RGs. (B) Shown at the top is the optical z-plane showing NGP electroporated with a GFP-CAAX-encoding plasmid (green), together with an immunostaining for GS (magenta) and Sox2 (blue). On the bottom is a sagittal view through a 3D reconstruction, highlighting the presence of a basal process on electroporated NGPs (green) and GS+ RGs (magenta). (C) Examples of NGP cell morphology. (D) Typical RG morphology, showing the ramified pattern of the basal process. Individual cells were manually detoured on a 3D reconstruction to visualize their morphologies. (E) Optical z-plane showing immunostaining for GS (green), Sox2 (blue) and PCNA (magenta), and EdU detection (cyan), on the high magnification of the pallial surface at 9 dph. White arrows point to non-cycling RG cells. (F) Proportion of PCNA+ cells among RGs (green bars) and NGPs (blue bars) at 2, 5, 9, and 14 dph. (G) Proportion of EdU+ cells among PCNA+ cells among RGs (green bars) and NGPs (blue bars). ∗Corrected p value < 0.05; two-way ANOVA, followed by pairwise comparisons using Holm’s procedure. Data were rank transformed prior to analysis. Data are represented as mean ± SEM; n = 6, 5, 5, and 3 for 2, 5, 9, and 14 dph, respectively. Scale bars, 50 μm in (A) and (E); 20 μm in (A’), (A’’), and (B); and 10 μm in (C) and (D). See also |