To assess the sensitivity of immunofluorescence staining in sections briefly fixed by immersion after ACSF fixation, we investigated the distribution of the GABAAR α1 and α3 subunits in relation to neuroligin 2, gephyrin and VGAT in the cerebellum of adult mice. In addition, to determine which neuron

type expresses the α3 subunit, we analysed sections from GlyT2-GFP mice (Zeilhofer et al., 2005), in which a large subpopulation of Golgi cells are distinctly eGFP-positive. The results, illustrated in Fig. 5, revealed that upon brief immersion-fixation Talazoparib price (60–90 min), postsynaptic GABAergic markers exhibit a bright, punctate staining, with high signal-to-noise ratio, thereby precisely revealing the distribution of presumptive GABAergic synapses on the cell body of Purkinje cells and in the molecular layer. While the GABAAR α1 subunit was colocalised extensively with neuroligin 2 (Fig. 5A and A′), the α3 subunit was present in only a small subset of GABAergic synapses located on dendrites in the molecular layer (Fig. 5B). Co-staining with gephyrin confirmed the postsynaptic localisation of the α3 subunit (Fig. 5C and C′), whereas parvalbumin double-labeling a marker of both, Purkinje cells and molecular layer interneurons

(Celio, 1990) confirmed that the α3 subunit-immunoreactivity was not located in parvalbumin-positive neurons (Fig. 5D). Examination of sections from GlyT2-GFP mice revealed that the α3 subunit Z-IETD-FMK clinical trial 3-oxoacyl-(acyl-carrier-protein) reductase clusters were present on the soma and dendrites of glycinergic Golgi cells (Fig. 5E and E′; Simat et al., 2007), and their postsynaptic localisation was confirmed by staining with VGAT (Fig. 5F and F′). As noted above for Fig. 2B and C, a longer immersion-fixation time (up to 3 h) was deleterious for the detection of synaptic proteins, albeit the effects were variable among

the antibodies tested. Presynaptic markers, such as VGAT and VGluT1, showed little influence of fixation time, whereas postsynaptic proteins, such as neuroligin 2 and gephyrin, were highly sensitive to the duration of fixation. Therefore, in our hands, immersion-fixation for 60–90 min represented an optimal duration for good quality staining and preservation of sections after the staining procedure. Taken together, these results underline the remarkable sensitivity of immunofluorescence staining and morphological preservation obtained in sections from ACSF-perfused mice, immersion-fixed for a short duration. Until now, the subcellular distribution of postsynaptic α3 subunit clusters could not be resolved satisfactorily in the cerebellum (Fritschy & Panzanelli, 2006), whereas here it is unambiguously demonstrated in a subpopulation of Golgi cells.