Finally, short- and long-term changes in the synaptic efficacy of GC-SC inputs (Bender et al., 2009, Dittman et al., 2000, Jörntell and Ekerot, 2002 and Kreitzer and Regehr, 2002) would alter the spatiotemporal filter properties

Src inhibitor of SCs, and contribute to the adaptive filter behavior of the cerebellar cortex (Dean et al., 2010). It is thought that partial somatotopy can be encoded in clusters of GC ascending synapses, which are organized in modules (Bower, 2010 and Ruigrok, 2011), but whether GCs convey different information to either proximal or distal regions of single SCs is unknown. Clonal studies show that GCs that develop at similar times extend their parallel fibers preferentially to specific

depths within the molecular layer (Espinosa and Luo, 2008). These authors show that the developmental stacking parallels the different developmental stages of the specific sensory modality innervation of the GC layer. As SCs dendrites protrude toward the pia in a biased manner (Sultan and Bower, 1998), it is conceivable that the different modalities exhibit a biased distribution within the SC dendritic tree, and may therefore experience different degrees of dendritic filtering. Nevertheless, the decorrelation properties of SCs suggest that their output firing will be biased in favor of sparse 17-AAG ic50 spatiotemporal patterns of its GC inputs. Physiological and anatomical evidence indicate that SC feed-forward inhibition is spatially organized to inhibit PCs that are adjacent to the activated interneuron and PC (Dizon and Khodakhah, 2011, Eccles et al., 1967, Ekerot and Jörntell, 2001, Jörntell et al., 2010, Sultan and Bower, 1998 and Szentagothai,

1965). This surround inhibition will provide a relative enhancement of the activity of PCs that for receive the same GC input as the activated SC. In particular, PCs receiving sparse rather than clustered synaptic activation patterns will experience a contrast enhancement of their response. It is therefore conceivable that the SC dendritic filtering can contribute to the sparse coding of GC-PC transmission, a feature thought to be important for the storage of a large number of activity patterns in PF-PC synaptic plasticity (Albus, 1971, Brunel et al., 2004 and Marr, 1969). Whole-cell patch-clamp recordings were made from SCs (33°C–36°C) located in the outer one-third of acutely prepared cerebellar slices from animals aging between P28 and P78 (200 μm thick). EPSCs and EPSPs were recorded with a Multiclamp-700B amplifier (Molecular Devices) and digitized using a multifunction input/output board (National Instruments). Data acquisition and analysis were performed using Neuromatic (www.neuromatic.thinkrandom.com) written within the Igor Pro 6.