TY - JOUR
T1 - Raising cytosolic Cl- in cerebellar granule cells affects their excitability and vestibulo-ocular learning
AU - Seja, P
AU - Schonewille, martijn
AU - Spitzmaul, G
AU - Badura, Aleksandra
AU - Klein, I
AU - Rudhard, Y
AU - Wisden, W
AU - Hubner, CA
AU - de Zeeuw, Chris
AU - Jentsch, TJ
PY - 2012
Y1 - 2012
N2 - Cerebellar cortical throughput involved in motor control comprises granule cells (GCs) and Purkinje cells (PCs), both of which receive inhibitory GABAergic input from interneurons. The GABAergic input to PCs is essential for learning and consolidation of the vestibulo-ocular reflex, but the role of GC excitability remains unclear. We now disrupted the Kcc2 K-Cl cotransporter specifically in either cell type to manipulate their excitability and inhibition by GABA(A)-receptor Cl- channels. Although Kcc2 may have a morphogenic role in synapse development, Kcc2 disruption neither changed synapse density nor spine morphology. In both GCs and PCs, disruption of Kcc2, but not Kcc3, increased [Cl-](i) roughly two-fold. The reduced Cl- gradient nearly abolished GABA-induced hyperpolarization in PCs, but in GCs it merely affected excitability by membrane depolarization. Ablation of Kcc2 from GCs impaired consolidation of long-term phase learning of the vestibulo-ocular reflex, whereas baseline performance, short-term gain-decrease learning and gain consolidation remained intact. These functions, however, were affected by disruption of Kcc2 in PCs. GC excitability plays a previously unknown, but specific role in consolidation of phase learning. The EMBO Journal (2012) 31, 1217-1230. doi: 10.1038/emboj.2011.488; Published online 17 January 2012
AB - Cerebellar cortical throughput involved in motor control comprises granule cells (GCs) and Purkinje cells (PCs), both of which receive inhibitory GABAergic input from interneurons. The GABAergic input to PCs is essential for learning and consolidation of the vestibulo-ocular reflex, but the role of GC excitability remains unclear. We now disrupted the Kcc2 K-Cl cotransporter specifically in either cell type to manipulate their excitability and inhibition by GABA(A)-receptor Cl- channels. Although Kcc2 may have a morphogenic role in synapse development, Kcc2 disruption neither changed synapse density nor spine morphology. In both GCs and PCs, disruption of Kcc2, but not Kcc3, increased [Cl-](i) roughly two-fold. The reduced Cl- gradient nearly abolished GABA-induced hyperpolarization in PCs, but in GCs it merely affected excitability by membrane depolarization. Ablation of Kcc2 from GCs impaired consolidation of long-term phase learning of the vestibulo-ocular reflex, whereas baseline performance, short-term gain-decrease learning and gain consolidation remained intact. These functions, however, were affected by disruption of Kcc2 in PCs. GC excitability plays a previously unknown, but specific role in consolidation of phase learning. The EMBO Journal (2012) 31, 1217-1230. doi: 10.1038/emboj.2011.488; Published online 17 January 2012
U2 - 10.1038/emboj.2011.488
DO - 10.1038/emboj.2011.488
M3 - Article
C2 - 22252133
SN - 0261-4189
VL - 31
SP - 1217
EP - 1230
JO - EMBO Journal
JF - EMBO Journal
IS - 5
ER -