Evidence map›Paper›PMID 15872106›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Key role of the postsynaptic density scaffold proteins Shank and Homer in the functional architecture of Ca2+ homeostasis at dendritic spines in hippocampal neurons.

Carlo Sala, Gautier Roussignol, Jacopo Meldolesi, Laurent Fagni

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 157 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  14. Proteomic Analysis of Post-synaptic Density Fractions fromFrontiers in molecular neuroscience · 2017
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Carlo SalaCellular and Molecular Pharmacology Section, Institute of Neuroscience, Consiglio Nazionale delle Ricerche, and Department of Pharmacology, University of Milan, 20129 Milan, Italy. c.sala@in.cnr.it
Gautier Roussignol
Jacopo Meldolesi
Laurent Fagni
École Normale Supérieure - PSL · FRIRCCS Ospedale San Raffaele · ITNeuroscience Institute · IT

Funding

Telethon GGP030234
6 · The paper itself

Abstract

A key aspect of postsynaptic function, also important for plasticity, is the segregation within dendritic spines of Ca2+ rises attributable to release from intracellular stores. Previous studies have shown that overexpression in hippocampal neurons of two postsynaptic density (PSD) scaffold proteins, Shank1B and Homer1b, induces spine maturation, including translocation of the intracellular Ca2+ channel inositol trisphosphate receptor (IP3R). The structural and functional significance of these processes remained undefined. Here, we show that in its relocation, IP3R is accompanied by other endoplasmic reticulum (ER) proteins: the Ca2+ pump sarcoendoplasmic reticulum calcium ATPase, the lumenal Ca2+-binding protein calreticulin, the ER lumen-addressed green fluorescent protein, and, to a lesser extent, the membrane chaperone calbindin. The specificity of these translocations was demonstrated by their inhibition by both a Shank1 fragment and the dominant-negative Homer1a. Activation in Shank1B-transfected neurons of the metabotropic glutamatergic receptors 1/5 (mGluRs1/5), which induce IP3 generation with ensuing Ca2+ release from the stores, triggered considerable increases in Ca2+-dependent responses: activation of the big K+ channel, which was revealed by patch clamping, and extracellular signal-regulated protein kinase (ERK) phosphorylation. The interaction of Shank1B and Homer1b appears as the molecular mechanism linking mGluRs1/5, strategically located in the spines, to IP3R with the integration of entire ER cisternas in the PSD and with consequences on both local Ca2+ homeostasis and overall neuronal signaling.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCalbindinsCalciumCalcium-Transporting ATPasesCalreticulinCarrier ProteinsCells, CulturedDendritic SpinesEmbryo, MammalianEndoplasmic ReticulumGene ExpressionGreen Fluorescent ProteinsHippocampusHomeostasisHomer Scaffolding Proteins3,4-dihydroxyphenylglycolAdaptor Proteins, Signal TransducingCalbindinsCalciumCalcium-Transporting ATPasesCalreticulinCarrier ProteinsGreen Fluorescent ProteinsHomer Scaffolding ProteinsMethoxyhydroxyphenylglycolMitogen-Activated Protein Kinase 3Nerve Tissue ProteinsReceptor, Metabotropic Glutamate 5Receptors, Metabotropic GlutamateS100 Calcium Binding Protein GSarcoplasmic Reticulum Calcium-Transporting ATPasesShank1 protein, rat

Identifiers

PMID15872106
PMCPMC6725036
OpenAlexW2021168371

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.