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. 2010 Mar 3;30(9):3489–3498. doi: 10.1523/JNEUROSCI.4987-09.2010

Figure 4.

Figure 4.

Increase in the number of transit-amplifying cells and neuroblasts in the Rbpj-mutant adult brain. A–N, Coronal sections of the SVZ of the lateral ventricles of control (A–G) and Rbpj-conditional knock-out (H–N) mice that were treated with tamoxifen 3 weeks before. BrdU was administered for 2 h before mice were killed. The number of BrdU-incorporated cells in the SVZ significantly increased in Rbpj-mutant mice (H–K) compared with controls (A–D). The number of Mash1+ transit-amplifying cells also increased in Rbpj-mutant mice (L, M) compared with controls (E, F). Boxed regions in panels E and L are enlarged in F and M, respectively. Neurogenesis (DCX+) was enhanced in Rbpj-mutants (N) compared with controls (G).