Evidence map›Paper›PMID 20865153›Full record

ArticlePLoS computational biology2010

Nonlinear gap junctions enable long-distance propagation of pulsating calcium waves in astrocyte networks.

Mati Goldberg, Maurizio De Pittà, Vladislav Volman, Hugues Berry, Eshel Ben-Jacob

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.9field-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

48 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
  2. Context-Dependent modulation of astrocytic CaJournal of computational neuroscience · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Astrocytes and Tinnitus.Brain sciences · 2024
    Review
  8. Article
  9. Photocatalytic manipulation of CaScience advances · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. A complete biomechanical model ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Neuron-Glia Interactions and Brain Circuits.Advances in experimental medicine and biology · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 3 countries.

Mati GoldbergSchool of Physics and Astronomy, Tel Aviv University, Ramat Aviv, Israel.
Maurizio De Pittà
Vladislav Volman
Hugues Berry
Eshel Ben-Jacob
Tel Aviv University · ILInstitut national de recherche en informatique et en automatique · FRSalk Institute for Biological Studies · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new paradigm has recently emerged in brain science whereby communications between glial cells and neuron-glia interactions should be considered together with neurons and their networks to understand higher brain functions. In particular, astrocytes, the main type of glial cells in the cortex, have been shown to communicate with neurons and with each other. They are thought to form a gap-junction-coupled syncytium supporting cell-cell communication via propagating Ca(2+) waves. An identified mode of propagation is based on cytoplasm-to-cytoplasm transport of inositol trisphosphate (IP(3)) through gap junctions that locally trigger Ca(2+) pulses via IP(3)-dependent Ca(2+)-induced Ca(2+) release. It is, however, currently unknown whether this intracellular route is able to support the propagation of long-distance regenerative Ca(2+) waves or is restricted to short-distance signaling. Furthermore, the influence of the intracellular signaling dynamics on intercellular propagation remains to be understood. In this work, we propose a model of the gap-junctional route for intercellular Ca(2+) wave propagation in astrocytes. Our model yields two major predictions. First, we show that long-distance regenerative signaling requires nonlinear coupling in the gap junctions. Second, we show that even with nonlinear gap junctions, long-distance regenerative signaling is favored when the internal Ca(2+) dynamics implements frequency modulation-encoding oscillations with pulsating dynamics, while amplitude modulation-encoding dynamics tends to restrict the propagation range. As a result, spatially heterogeneous molecular properties and/or weak couplings are shown to give rise to rich spatiotemporal dynamics that support complex propagation behaviors. These results shed new light on the mechanisms implicated in the propagation of Ca(2+) waves across astrocytes and the precise conditions under which glial cells may participate in information processing in the brain.

Indexed as

Models, NeurologicalAstrocytesBrainCalcium SignalingGap JunctionsHumansInositol 1,4,5-TrisphosphateNerve NetInositol 1,4,5-Trisphosphate

Identifiers

PMID20865153
PMCPMC2928752
OpenAlexW2065705799

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.