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. 2009 Apr 20;106(19):7876–7881. doi: 10.1073/pnas.0902750106

Fig. 2.

Fig. 2.

Neuronal defects in HDAC1loxP/loxP; HDAC2loxP/loxP; GFAP-Cre mice. (A) Immunohistochemical staining of MAP-2 on the neocortex of wild-type and mutant mice. Mutant mice show a lack of dendritic extensions compared with control. Scale bar = 40 μm. (B) Immunohistochemical staining for calbindin on wild-type and mutant cerebellum. Mutant cerebellum shows Purkinje cells have failed to migrate and remain among the deep cerebellar nuclei. Scale bar = 40 μm. (C) Immunohistochemistry of CSPGs (green) and Hoechst (blue) of wild-type and mutant cerebral cortex and hippocampus. Scale bar = 40 μm. Deletion of HDAC1 and HDAC2 results in disorganized molecular layers. Hippocampal structures are unidentifiable in mutant mice. MZ, marginal zone; CP, cortical plate; SP, subplate; IZ, intermediate zone; VZ, ventricular zone.