Ca-permeable AMPA receptors in homeostatic synaptic plasticity - PubMed
- ️Sun Jan 01 2012
Ca-permeable AMPA receptors in homeostatic synaptic plasticity
Hey-Kyoung Lee. Front Mol Neurosci. 2012.
Abstract
Neurons possess diverse mechanisms of homeostatic adaptation to overall changes in neural and synaptic activity, which are critical for proper brain functions. Homeostatic regulation of excitatory synapses has been studied in the context of synaptic scaling, which allows neurons to adjust their excitatory synaptic gain to maintain their activity within a dynamic range. Recent evidence suggests that one of the main mechanisms underlying synaptic scaling is by altering the function of postsynaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs), including synaptic expression of Ca(2+)-permeable (CP-) AMPARs. CP-AMPARs endow synapses with unique properties, which may benefit adaptation of neurons to periods of inactivity as would occur when a major input is lost. This review will summarize how synaptic expression of CP-AMPARs is regulated during homeostatic synaptic plasticity in the context of synaptic scaling, and will address the potential functional consequences of altering synaptic CP-AMPAR content.
Keywords: CP-AMPAR; GluA1; activity-dependent; homeostasis; inactivity; synaptic scaling.
Figures

Regulation of CP-AMPARs in homeostatic synaptic plasticity. (A) Inactivity-induced synaptic expression of CP-AMPARs. Inactivity leads to local synthesis of GluA1. One mechanism is via RA signaling, where RA binds to RARα to relieve translational inhibition of GluA1 mRNA. Newly synthesized GluA1 containing CP-AMPARs are then eventually trafficked to the synapse (PSD, postsynaptic density). Cell surface expression of GluA1 containing CP-AMPARs is likely tied to phosphorylation of GluA1-S845. In visual cortex, the increase in extrasynaptic GluA1 leads to synaptic accumulation, however, in hippocampus an extra regulatory step from perisynaptic to synaptic trafficking may be needed. Inactivity driven synaptic localization of CP-AMPARs also depend on CaMKIIβ activity, which may act on GluA1-S831 phosphorylation. Synaptic expression of CP-AMPARs may occur in conjunction with removal of CI-AMPARs via GluA2-dependent mechanisms. (B) Removal of synaptic CP-AMPARs following an increase in neural activity. The increase in neuronal activity following a period of inactivity results in up-regulation of immediate early genes such as Arc and Homer1a. Both of these proteins lead to endocytosis of AMPARs. However, this process is not likely specific to CP-AMPARs and would result in removal of CI-AMPARs as well (not depicted in the figure). Homer1a acts to produce agonist-independent activation of Group 1 mGluRs by displacing long forms of Homer1. Homer1a signaling is specific for activity-dependent homeostatic scaling down of excitatory synapses. On the other hand, Arc is also involved in AMPAR endocytosis following mGluR-LTD.
Similar articles
-
Sanderson JL, Scott JD, Dell'Acqua ML. Sanderson JL, et al. J Neurosci. 2018 Mar 14;38(11):2863-2876. doi: 10.1523/JNEUROSCI.2362-17.2018. Epub 2018 Feb 13. J Neurosci. 2018. PMID: 29440558 Free PMC article.
-
Purkey AM, Dell'Acqua ML. Purkey AM, et al. Front Synaptic Neurosci. 2020 Mar 27;12:8. doi: 10.3389/fnsyn.2020.00008. eCollection 2020. Front Synaptic Neurosci. 2020. PMID: 32292336 Free PMC article.
-
Non-scaling regulation of AMPA receptors in homeostatic synaptic plasticity.
Wang G, Zhong J, Guttieres D, Man HY. Wang G, et al. Neuropharmacology. 2019 Nov 1;158:107700. doi: 10.1016/j.neuropharm.2019.107700. Epub 2019 Jul 5. Neuropharmacology. 2019. PMID: 31283924 Free PMC article.
-
The AMPA Receptor Code of Synaptic Plasticity.
Diering GH, Huganir RL. Diering GH, et al. Neuron. 2018 Oct 24;100(2):314-329. doi: 10.1016/j.neuron.2018.10.018. Neuron. 2018. PMID: 30359599 Free PMC article. Review.
-
Whitehead G, Regan P, Whitcomb DJ, Cho K. Whitehead G, et al. Neuropharmacology. 2017 Jan;112(Pt A):221-227. doi: 10.1016/j.neuropharm.2016.08.022. Epub 2016 Aug 22. Neuropharmacology. 2017. PMID: 27561971 Review.
Cited by
-
Park MJ, Seo BA, Lee B, Shin HS, Kang MG. Park MJ, et al. Sci Rep. 2018 Oct 9;8(1):15008. doi: 10.1038/s41598-018-33410-1. Sci Rep. 2018. PMID: 30301947 Free PMC article.
-
Schormans AL, Typlt M, Allman BL. Schormans AL, et al. Cereb Cortex. 2019 May 1;29(5):1875-1888. doi: 10.1093/cercor/bhy067. Cereb Cortex. 2019. PMID: 29668848 Free PMC article.
-
Ouyang J, Carcea I, Schiavo JK, Jones KT, Rabinowitsch A, Kolaric R, Cabeza de Vaca S, Froemke RC, Carr KD. Ouyang J, et al. Eur J Neurosci. 2017 Mar;45(6):826-836. doi: 10.1111/ejn.13528. Epub 2017 Feb 15. Eur J Neurosci. 2017. PMID: 28112453 Free PMC article.
-
In vivo synaptic scaling is mediated by GluA2-lacking AMPA receptors in the embryonic spinal cord.
Garcia-Bereguiain MA, Gonzalez-Islas C, Lindsly C, Butler E, Hill AW, Wenner P. Garcia-Bereguiain MA, et al. J Neurosci. 2013 Apr 17;33(16):6791-9. doi: 10.1523/JNEUROSCI.4025-12.2013. J Neurosci. 2013. PMID: 23595738 Free PMC article.
-
Distinct sensory requirements for unimodal and cross-modal homeostatic synaptic plasticity.
He K, Petrus E, Gammon N, Lee HK. He K, et al. J Neurosci. 2012 Jun 20;32(25):8469-74. doi: 10.1523/JNEUROSCI.1424-12.2012. J Neurosci. 2012. PMID: 22723686 Free PMC article.
References
LinkOut - more resources
Full Text Sources
Miscellaneous