, 2008). Accordingly, confocal line-scan imaging illustrated the colocalization of labeling for both antibodies at single puncta, suggesting that both connexins coexist at individual plaques (Figure 1H). We quantified the colocalization of Cx35 with Cx34.7 (and vice versa) using confocal reconstruction of individual terminals, as identified by shape and Cx35 labeling (Figure 1F). Averaged over individual endings, 85.04% (±9.12 SD) of the area MK-2206 supplier of Cx35 immunolabeling also showed Cx34.7 labeling and 81.23% (±8.34 SD) of the area of Cx34.7 labeling showed Cx35 labeling (n = 30) (Figure 1I). Thus, although not completely overlapping,

the two proteins exhibit a high degree of colocalization in CEs. To confirm that Cx35 and Cx34.7 colocalize at individual GJ plaques, we performed conventional freeze-fracture

replica immunogold labeling (FRIL), which allows broad expanses of tissues to be examined and facilitates unambiguous assignment of specific connexin labeling to GJ selleck products hemiplaques in either of two apposed cells (see Supplemental Experimental Procedures). Four replicas of goldfish hindbrain contained CE synapses on identified M-cells. The CE terminals were identified on confocal grid-mapped M-cells that had been injected with Lucifer yellow during in vivo recordings prior to tissue fixation as well as in one set of matched double replicas prepared by SDS-FRIL (see Supplemental Experimental Procedures). Samples were either single-labeled with anti-Cx36 Ab298, which binds to both Cx34.7 and Cx35 (see below), or double-labeled for Cx35 and Cx34.7 IL. In a double-labeled replica of a positively identified M-cell, labeling for Cx35 was found directly associated with GJ plaques in presynaptic membranes of CEs (n = 20 GJs). In contrast, labeling for Cx34.7 was only on identified M-cell postsynaptic membranes (n = 53 GJs). Consistent

with this distribution, anti-Cx36 Ab298, which recognizes both Cx35 and Cx34.7 (see next section and Table S1), was found to label both pre- and postsynaptic membranes (data not crotamiton shown, but see data in Pereda et al., 2003). Such differential distribution to pre- versus postsynaptic membranes was investigated further by double-immunolabeling for Cx35 and Cx34.7 using matched double-replica FRIL (DR-FRIL). Initially, a sample prepared for DR-FRIL was fractured and major portions of both matching complements were retrieved and labeled. In one of the two M-cell complements, more than 400 labeled GJs were found; 367 were viewed toward the M-cell side of the junction (Figures 2A–2D), all of which were labeled for Cx34.7 and none for Cx35; and 79 were viewed from the M-cell side of the synapse toward the CE (Figure 2E), all of which were labeled for Cx35 and none for Cx34.7. A diagram of that same cell is indicated in Figures 2F and 2G, illustrating the two primary views seen in Figures 2D and 2E.