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. 2021 Aug 24;36(8):109588. doi: 10.1016/j.celrep.2021.109588

Figure 4.

Figure 4

Effects of Zeb1 loss in newborn neurons

(A) Representative images of DCX+tdTOM+ neuroblasts (arrows) at 2 weeks post-induction.

(B) Quantification of DCX+tdTOM+ neuroblasts in the DG of control and Zeb1−/− mice at 2, 4, and 8 weeks post-induction.

(C) Summary graph of neuroblast changes over time.

(D) Representative images of NeuN+ granule neurons (arrows) at 4 weeks post-induction.

(E) Numbers of NeuN+tdTOM+ granule neurons at 4, 8, and 12 weeks post-induction.

(F) Summary graph showing granule neuron changes over time.

(G) 2D projection of a two-photon image z stack showing a typical granule cell filled with Alexa 488 via the patch-clamp recording electrode. Representative recordings from tdTOM expressing Zeb1−/− (red) and control (blue) DGGCs.

(H) Scatterplots show resting membrane potential (Rm), input resistance (RN), membrane time constant (τm), and membrane capacitance (Cm) for individual DGGCs overlaid with the mean for each group.

Additional graphs and Neurolucida traces are in Figure S3. Dots represent individual mice (minimum of two sections analyzed per animal; B and E), average values (C and F), or individual neurons (4 mice/genotype, H). Numerical data are shown as mean ± SEM. Scale bars: 20 μm (insets: 10 μm). See also Figures S2 and S3.