Skip to main content
. 2016 Mar 16;5:e09862. doi: 10.7554/eLife.09862

Figure 5. Spatial organization of granule cell (GC) input patterns to molecular interneurons and Golgi cells is distinct from GC input maps to Purkinje cells.

(A) Median granule cell (GC) input pattern to Golgi cells (GoCs; Z-score of charge) for GoCs located at the same location as Purkinje cells (PCs) from cluster 1. Black: Z-score <3.09, orange: Z-score >3.09. Error bars are in light gray. Inset: overlay of all 3D-reconstructed GoCs, showing the extension of the axonal plexus, that is, the maximal region in which GoCs could inhibit GCs (same scale as the median pattern). (B) Median GC input pattern to molecular interneurons (MLIs; Z-score of number of excitatory post-synaptic currents, EPSCs) at the same position as PCs from cluster 1. The upward arrow indicates a hotspot of GCs contacting MLIs located in the cluster 1 region, but not PCs. Inset: example of EPSCs recorded following photostimulation. Stars indicate detected EPSCs.

DOI: http://dx.doi.org/10.7554/eLife.09862.011

Figure 5.

Figure 5—figure supplement 1. Spatial organization of granule cell input patterns to Golgi cells recorded in the area of cluster 2,3 and 4 for Purkinje cells.

Figure 5—figure supplement 1.

Upper panel: histogram of the median Z-score for Golgi cells (GoCs) recorded in clusters 2, 3 and 4 of Purkinje cells (PCs). Lower panel: reconstruction of GoC recorded in P1 close to the P1+ boundary. Note that the axon crosses two zebrin band boundaries. Scale bar, 50 μm.