Evidence map›Paper›PMID 31324651›Full record

ArticleThe Journal of general physiology2019

Dendritic spine geometry and spine apparatus organization govern the spatiotemporal dynamics of calcium.

Miriam Bell, Tom Bartol, Terrence Sejnowski, Padmini Rangamani

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
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  7. Nano-organization of synaptic calcium signaling.Biochemical Society transactions · 2024
    Review
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  17. Control of CaGlia · 2022
    Article
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  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Miriam BellDepartment of Mechanical and Aerospace Engineering, University of California, San Diego, La Jolla, CA.
Tom BartolHoward Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, CA.
Terrence SejnowskiHoward Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, CA.
Padmini RangamaniDepartment of Mechanical and Aerospace Engineering, University of California, San Diego, La Jolla, CA padmini.rangamani@eng.ucsd.edu.ORCID 0000-0001-5953-4347
Salk Institute for Biological Studies · USUniversity of California San Diego · US

Funding

Training in Multi-Scale Analysis of Biological Structure and FunctionT32EB009380 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrew D. McCulloch, Padmini Rangamani · 2009 to 2026
$4.8M
CRCNS: Regulating AMPAR trapping and desensitization in the postsynaptic density R01MH115556 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SEJNOWSKI, TERRENCE J · 2017 to 2020
$1.2M
NIBIB NIH HHS T32 EB009380NIMH NIH HHS R01 MH115556
6 · The paper itself

Abstract

Dendritic spines are small subcompartments that protrude from the dendrites of neurons and are important for signaling activity and synaptic communication. These subcompartments have been characterized to have different shapes. While it is known that these shapes are associated with spine function, the specific nature of these shape-function relationships is not well understood. In this work, we systematically investigated the relationship between the shape and size of both the spine head and spine apparatus, a specialized endoplasmic reticulum compartment within the spine head, in modulating rapid calcium dynamics using mathematical modeling. We developed a spatial multicompartment reaction-diffusion model of calcium dynamics in three dimensions with various flux sources, including N-methyl-D-aspartate receptors (NMDARs), voltage-sensitive calcium channels (VSCCs), and different ion pumps on the plasma membrane. Using this model, we make several important predictions. First, the volume to surface area ratio of the spine regulates calcium dynamics. Second, membrane fluxes impact calcium dynamics temporally and spatially in a nonlinear fashion. Finally, the spine apparatus can act as a physical buffer for calcium by acting as a sink and rescaling the calcium concentration. These predictions set the stage for future experimental investigations of calcium dynamics in dendritic spines.

Indexed as

Calcium SignalingModels, TheoreticalAnimalsCalciumCalcium ChannelsDendritic SpinesRatsReceptors, N-Methyl-D-AspartateCalciumCalcium ChannelsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID31324651
PMCPMC6683673
OpenAlexW2963381503

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.