Figure 7: Fate tracing of multipotent progenitors in the cochlea during development. | Nature Communications

Figure 7: Fate tracing of multipotent progenitors in the cochlea during development.

From: Identification of mouse cochlear progenitors that develop hair and supporting cells in the organ of Corti

Figure 7

(a) Co-immunostaining for Neurod1 (green) and Myo7a (blue) of Eya1CreER;Rainbow cochlea (2 mg tamoxifen given at E13.5). Arrows point to partial overlap of Neurod1 labelling with RFP in Eya1-lineage marked spiral ganglion cells, which is most likely due to different cells either closely intertwined or at different focal planes. (b) Co-immunostaining with anti-β-Gal (green) and -Neurod1 (red) on section of wild-type spiral ganglion region (SPG) at E13.5. (c) LacZ staining of Eya1LacZ cochlea at E14.5 showing Neurod1− high LacZ (Eya1)+ cells in the SPG (arrows). (d) Co-immunostaining for Neurod1 (red) and β-Gal (green) on section from Eya1CreER;R26RLacZ cochleae at P0 (3 mg tamoxifen at E12.5). Arrows point to a few Neurod1+ Eya1-lineage marked cells in the SPG. (e) Co-immunostaining for NF (red) and β-Gal (green) on section from Eya1CreER;R26RLacZ cochleae at P0 (3 mg tamoxifen at E12.5). Open arrowhead points to Eya1-lineage marked cells on the nerve fibres projecting to the OC. (f) Co-immunostaining for Neurod1 (green) and Myo7a (blue) of RosaCreER;Rainbow cochlea (∼2 mg tamoxifen given at E12.5). Scale bars: 50 μm.

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