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Epidermal growth factor receptor pathway substrate 8 (Eps8) is a widely expressed multidomain signaling protein that coordinates two disparate GTPase-dependent mechanisms: actin reorganization via Ras/Rac pathways and receptor trafficking via Rab5. Expression of Eps8, the gene encoding the founding member of the Eps8 family of proteins, was found in cerebellum by virtual Northern analysis and in situ hybridization. Because the cerebellum has a well-known cellular architecture and is a favored model to study synaptic plasticity and actin dynamics, we sought to analyze Eps8 localization in rat cerebellar neurons and synapses by light and electron microscopy. Specificity of Eps8-antibody was demonstrated by immunoblots and in brain sections. In cerebellum, unipolar brush cells (UBCs) were densely Eps8 immunopositive and granule cells were moderately immunostained. In both types of neuron immunoreaction product was localized to the somatodendritic and axonal compartments. Postsynaptic immunostained foci were demonstrated in the glomeruli in correspondence of the synapses formed by mossy fiber terminals with granule cell and UBC dendrites. These foci appeared especially evident in the UBC brush, which contains an extraordinary postsynaptic apparatus of actin microfilaments facing synaptic junctions of the long and segmented varieties. Eps8 immunoreactivity was conspicuously absent in Purkinje cells and their actin-rich dendritic spines, in all types of inhibitory interneurons of the cerebellum, cerebellar nuclei neurons, and astrocytes. In conclusion, Eps8 protein in cerebellum is expressed exclusively by excitatory cortical interneurons and is intracellularly compartmentalized in a cell-class specific manner. This is the first demonstration of the presence of a member of the Eps8 protein family in UBCs and its enrichment at postsynaptic sites.

Cerebellar morphogenesis occurs through a complex interplay of cell proliferation and migration that in mouse and rat begins about midgestation and ends in the third postnatal week. Cerebellar cells derive from germinative matrices in the ventricular zone and the external granular layer. Like granule cells, unipolar brush cells (UBCs) are excitatory interneurons situated in the granular layer of the cortex and innervated by mossy fibers. While granule cells are produced from the external granular layer, the generation of UBCs is still controversial. We utilized the reeler mutant mouse, which has widespread misplacement of neurons due to lack of Reelin protein, to ascertain the origin of UBCs. In the reeler cerebellum, which is small and lacks foliation, Purkinje cells are greatly reduced in number and in large part are located ectopically in deep cerebellar masses. Granule cells are also reduced in number and form an irregular granule cell layer. In this study we demonstrate that the reeler mutation influences the positioning of UBCs and also significantly reduces their number. Both subsets of UBCs identified in normal mouse, the calretinin-positive and the metabotropic glutamate receptor 1alpha-positive subsets, are affected in the reeler. About 40% of the calretinin-positive UBCs are ectopically situated in the deep cerebellar regions and the immediate vicinity of the ependyma of the fourth ventricle. Ectopic UBCs have discrete, although somewhat looser brushes than granular layer UBCs, but form synaptic junctions with complex axon terminals, possibly belonging to mossy fibers and UBC axons, like their normally situated counterpart. The observed displacement of UBCs in the reeler suggests that they originate from the ventricular zone.

Unipolar brush cells (UBCs) are a class of excitatory, glutamatergic interneurons occurring at high density in the granular layer of the vestibulo-cerebellum. UBCs are intermediate in size between granule cells, which in rat originate postnatally from precursors in the external granular layer, and Golgi cells, which are generated prenatally and postnatally from precursors in the ventricular zone that continue to divide while they migrate toward the cortex. The origin of the UBCs is still poorly understood. In this study, we set forth to ascertain the possible prenatal origin of UBCs, taking advantage of the immunocytochemical 5-bromo-2'-deoxyuridine (BrdU) method to label dividing cells in combination with antisera to cell population markers, that distinguish UBCs from granule and Golgi cells. Pregnant rat dams received six i.p. injections of BrdU (total 36 mg/animal) over 2 successive days at different stages of prenatal development (embryonic day [E]14/15-E20/21). Adult offspring were analyzed for histology. Using antibodies against the ionotropic glutamate receptor GluR2 and the calcium binding protein calretinin we found two populations of UBCs. A subset of about 30% of UBCs was calretinin and GluR2 positive, while the majority of the UBCs were calretinin negative and GluR2 positive. Results indicate that UBCs originate from precursors proliferating between E16 and E21. However, UBCs defined by calretinin immunoreactivity were primarily born in a narrow time window at E17-18. UBCs immunostained with antiserum to GluR2, but not labeled with calretinin were generated later, from E19 to E21. Our data also indicate that a part of GluR2 positive UBCs are born around and after E22. The subset of later born, calretinin negative UBCs may coincide with the pale cells, a group of cerebellar interneurons previously identified by [3H]thymidine labeling.