PKCλ is critical in AMPA receptor phosphorylation and synaptic incorporation during LTP
Direct phosphorylation of GluA1 by PKC controls α‐amino‐3‐hydroxy‐5‐methyl‐isoxazole‐4‐propionic acid (AMPA) receptor (AMPAR) incorporation into active synapses during long‐term potentiation (LTP). Numerous signalling molecules that involved in AMPAR incorporation have been identified, but the speci...
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Published in | The EMBO journal Vol. 32; no. 10; pp. 1365 - 1380 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
15.05.2013
Nature Publishing Group UK Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Direct phosphorylation of GluA1 by PKC controls α‐amino‐3‐hydroxy‐5‐methyl‐isoxazole‐4‐propionic acid (AMPA) receptor (AMPAR) incorporation into active synapses during long‐term potentiation (LTP). Numerous signalling molecules that involved in AMPAR incorporation have been identified, but the specific PKC isoform(s) participating in GluA1 phosphorylation and the molecule triggering PKC activation remain largely unknown. Here, we report that the atypical isoform of PKC, PKCλ, is a critical molecule that acts downstream of phosphatidylinositol 3‐kinase (PI3K) and is essential for LTP expression. PKCλ activation is required for both GluA1 phosphorylation and increased surface expression of AMPARs during LTP. Moreover, p62 interacts with both PKCλ and GluA1 during LTP and may serve as a scaffolding protein to place PKCλ in close proximity to facilitate GluA1 phosphorylation by PKCλ. Thus, we conclude that PKCλ is the critical signalling molecule responsible for GluA1‐containing AMPAR phosphorylation and synaptic incorporation at activated synapses during LTP expression.
PI3K‐mediated PKCλ activation promotes GluA1‐containing AMPAR phosphorylation and incorporation into postsynaptic site during LTP. |
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Bibliography: | istex:5D791D355E4A3CD9BA7CD35D9EF569E1D128E404 ark:/67375/WNG-VDNSBS7M-F Supplementary InformationReview Process FileSource data for Figure 1bSource data for Figure 2aSource data for Figure 2cSource data for Figure 3aSource data for Figure 3eSource data for Figure 4aSource data for Figure 4cSource data for Figure 4eSource data for Figure 4hSource data for Figure 5cSource data for Figure 5dSource data for Figure 6a ArticleID:EMBJ201360 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0261-4189 1460-2075 1460-2075 |
DOI: | 10.1038/emboj.2013.60 |