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. 2014 Jan 18;33(5):512–527. doi: 10.1002/embj.201385887

Figure 1.

Figure 1

Number of converging endbulbs and bassoon immunolocalization in the AVCN of Bsnwt and BsnΔEx4/5 mice.

A  Single confocal section from a stack (left) used for reconstruction of endbulb terminals (right, four endbulbs converging onto the BC in this example), immunolabeled for calretinin (red) as an endbulb marker, bassoon (green) as a marker for AZs and VGAT (blue) as a marker for inhibitory synapses.

B The number of endbulb terminals converging onto a BC remained unchanged in BsnΔEx4/5 mice (N, number of animals; n, number of BCs).

C Domain structure of bassoon and the BsnΔEx4/5 fragment including the epitopes utilized for immunolabeling.

D, E  Projection of a confocal image stack labeled for the two bassoon epitopes and piccolo of a Bsnwt (D) and a BsnΔEx4/5 (E) BC.

F  Number of puncta and fraction of colocalizing bassoon puncta (left, Bsn-sap7f AB; right Bsn-c-term. AB) with piccolo of two BC for each genotype.

G  Center of mass distance between all colocalizing Bsn-c-term. and piccolo puncta of the four cells depicted in (F), illustrating that the BsnΔEx4/5 fragment is not as tightly confined to AZs as wild-type bassoon.