PUBLICATION
PKC{gamma}-induced trafficking of AMPA receptors in embryonic zebrafish depends on NSF and PICK1
- Authors
- Patten, S.A., and Ali, D.W.
- ID
- ZDB-PUB-090417-7
- Date
- 2009
- Source
- Proceedings of the National Academy of Sciences of the United States of America 106(16): 6796-6801 (Journal)
- Registered Authors
- Keywords
- Mauthner neuron, glutamate, NMDA, synapse, development
- MeSH Terms
-
- Animals
- Carrier Proteins/metabolism*
- Embryo, Nonmammalian/cytology
- Embryo, Nonmammalian/enzymology*
- Enzyme Activation
- Excitatory Postsynaptic Potentials
- Miniature Postsynaptic Potentials
- N-Ethylmaleimide-Sensitive Proteins/metabolism*
- Protein Kinase C/metabolism*
- Protein Transport
- Receptors, AMPA/metabolism*
- Zebrafish/embryology*
- Zebrafish Proteins/metabolism*
- PubMed
- 19366675 Full text @ Proc. Natl. Acad. Sci. USA
Citation
Patten, S.A., and Ali, D.W. (2009) PKC{gamma}-induced trafficking of AMPA receptors in embryonic zebrafish depends on NSF and PICK1. Proceedings of the National Academy of Sciences of the United States of America. 106(16):6796-6801.
Abstract
The trafficking of AMPA receptors (Rs) to and from synaptic membranes is a key component underlying synaptic plasticity mechanisms such as long-term potentiation (LTP) and long-term depression (LTD), and is likely important for synaptic development in embryonic organisms. However, some of the key biochemical components required for receptor trafficking in embryos are still unknown. Here, we report that in embryonic zebrafish, the activation of PKCgamma by phorbol 12-myristate 13-acetate, strongly potentiates the amplitude of AMPAR-mediated miniature excitatory postsynaptic currents (AMPA-mEPSCs) via a N-ethylmaleimide-sensitive fusion (NSF) and protein interacting with C-kinase-1 (PICK1)-dependent process. We found that the mEPSC potentiation is DAG- and Ca(2+)-dependent, and occurs on application of active PKCgamma. Peptides that prevent the association of NSF and PICK1 with the GluR2 subunit, and the actin-polymerization blocker, latrunculin B, prevented the increase in mEPSC amplitude. Also, application of tetanus toxin (TeTx), which cleaves SNARE proteins, also blocked the increase in mEPSC amplitude. Last, application of a 5 mM K(+) medium led to an enhancement in mEPSC amplitude that was prevented by addition of the PKCgamma and NSF-blocking peptides, and the NMDA receptor blocker, 2-amino-5-phosphonovaleric acid (APV). Thus, activation of PKCgamma is necessary for the activity-dependent trafficking of AMPARs in embryonic zebrafish. This process is NMDA and SNARE-dependent and requires AMPARs to associate with both NSF and PICK1. The present data further our understanding of AMPAR trafficking, and have important implications for synaptic development and synaptic plasticity.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping