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Publication : Reassessment of long-term depression in cerebellar Purkinje cells in mice carrying mutated GluA2 C terminus.

First Author  Yamaguchi K Year  2016
Journal  Proc Natl Acad Sci U S A Volume  113
Issue  36 Pages  10192-7
PubMed ID  27551099 Mgi Jnum  J:235584
Mgi Id  MGI:5796864 Doi  10.1073/pnas.1609957113
Citation  Yamaguchi K, et al. (2016) Reassessment of long-term depression in cerebellar Purkinje cells in mice carrying mutated GluA2 C terminus. Proc Natl Acad Sci U S A 113(36):10192-7
abstractText  Long-term depression (LTD) of synaptic transmission from parallel fibers (PFs) to a Purkinje cell (PC) in the cerebellum has been considered to be a core mechanism of motor learning. Recently, however, discrepancies between LTD and motor learning have been reported in mice with a mutation that targeted the expression of PF-PC LTD by blocking AMPA-subtype glutamate receptor internalization regulated via the phosphorylation of AMPA receptors. In these mice, motor learning behavior was normal, but no PF-PC LTD was observed. We reexamined slices obtained from these GluA2 K882A and GluA2 Delta7 knockin mutants at 3-6 mo of age. The conventional protocols of stimulation did not induce LTD in these mutant mice, as previously reported, but surprisingly, LTD was induced using certain modified protocols. Such modifications involved increases in the number of PF stimulation (from one to two or five), replacement of climbing fiber stimulation with somatic depolarization (50 ms), filling a patch pipette with a Cs(+)-based solution, or extension of the duration of conjunction. We also found that intracellular infusion of a selective PKCalpha inhibitor (Go6976) blocked LTD induction in the mutants, as in WT, suggesting that functional compensation occurred downstream of PKCalpha. The possibility that LTD in the mutants was caused by changes in membrane resistance, access resistance, or presynaptic property was excluded. The present results demonstrate that LTD is inducible by intensified conjunctive stimulations even in K882A and Delta7 mutants, indicating no contradiction against the LTD hypothesis of motor learning.
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