A unique PDZ ligand in PKCα confers induction of cerebellar long-term synaptic depression

被引:96
作者
Leitges, M
Kovac, J
Plomann, M
Linden, DJ
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] Max Planck Inst Expt Endokrinol, D-30625 Hannover, Germany
[3] Univ Cologne, Ctr Biochem, D-50931 Cologne, Germany
关键词
D O I
10.1016/j.neuron.2004.10.024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Induction of cerebellar long-term depression (LTD) requires a postsynaptic cascade involving activation of mGluR1 and protein kinase C (PKC). Our understanding of this process has been limited by the fact that PKC is a large family of molecules, many isoforms of which are expressed in the relevant postsynaptic compartment, the cerebellar Purkinje cell. Here, we report that LTD is absent in Purkinje cells in which the alpha isoform of PKC has been reduced by targeted RNA interference or in cells derived from PKCalpha null mice. In both of these cases, LTD could be rescued by expression of PKCalpha but not other PKC isoforms. The special role of PKCa in cerebellar LTD is likely to derive from its unique PDZ ligand (OSAV). When this motif is mutated, PKCalpha no longer supports LTD. Conversely, when this PDZ ligand is inserted in a nonpermissive isoform, PKCgamma, it confers the capacity for LTD induction.
引用
收藏
页码:585 / 594
页数:10
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