XB-ART-55214
EMBO J
2018 Jan 04;371:122-138. doi: 10.15252/embj.201695829.
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Ca2+/calmodulin binding to PSD-95 mediates homeostatic synaptic scaling down.
Chowdhury D
,
Turner M
,
Patriarchi T
,
Hergarden AC
,
Anderson D
,
Zhang Y
,
Sun J
,
Chen CY
,
Ames JB
,
Hell JW
.
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Postsynaptic density protein-95 (PSD-95) localizes AMPA-type glutamate receptors (AMPARs) to postsynaptic sites of glutamatergic synapses. Its postsynaptic displacement is necessary for loss of AMPARs during homeostatic scaling down of synapses. Here, we demonstrate that upon Ca2+ influx, Ca2+/calmodulin (Ca2+/CaM) binding to the N-terminus of PSD-95 mediates postsynaptic loss of PSD-95 and AMPARs during homeostatic scaling down. Our NMR structural analysis identified E17 within the PSD-95 N-terminus as important for binding to Ca2+/CaM by interacting with R126 on CaM. Mutating E17 to R prevented homeostatic scaling down in primary hippocampal neurons, which is rescued via charge inversion by ectopic expression of CaMR126E, as determined by analysis of miniature excitatory postsynaptic currents. Accordingly, increased binding of Ca2+/CaM to PSD-95 induced by a chronic increase in Ca2+ influx is a critical molecular event in homeostatic downscaling of glutamatergic synaptic transmission.
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R01 AG055357 NIA NIH HHS , R01 EY012347 NEI NIH HHS , R01 MH097887 NIMH NIH HHS, R01 NS078792 NINDS NIH HHS
Species referenced: Xenopus laevis
Genes referenced: dlg4 epha8 gsk3b psd
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