Evidence map›Paper›PMID 27118849›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Astrocytes regulate heterogeneity of presynaptic strengths in hippocampal networks.

Mathieu Letellier, Yun Kyung Park, Thomas E Chater, Peter H Chipman, Sunita Ghimire Gautam, Tomoko Oshima-Takago, Yukiko Goda

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
  2. Article
  3. Astrocytic CaNature neuroscience · 2025
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  9. Equal levels of pre- and postsynaptic potentiation produce unequal outcomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
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  11. Review
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  19. A sequential two-step priming scheme reproduces diversity in synaptic strength and short-term plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

7 authors at 2 institutions in 1 country.

Mathieu LetellierBrain Science Institute, RIKEN, Saitama 351-0198, Japan; letellier.mathieu@gmail.com goda@brain.riken.jp.
Yun Kyung ParkBrain Science Institute, RIKEN, Saitama 351-0198, Japan;
Thomas E ChaterBrain Science Institute, RIKEN, Saitama 351-0198, Japan;
Peter H ChipmanBrain Science Institute, RIKEN, Saitama 351-0198, Japan;
Sunita Ghimire GautamBrain Science Institute, RIKEN, Saitama 351-0198, Japan;
Tomoko Oshima-TakagoBrain Science Institute, RIKEN, Saitama 351-0198, Japan;
Yukiko GodaBrain Science Institute, RIKEN, Saitama 351-0198, Japan; Saitama University Brain Science Institute, Saitama University, Saitama 338-8570, Japan; Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, Tokyo 153-8902, Japan letellier.mathieu@gmail.com goda@brain.riken.jp.
RIKEN Center for Brain Science · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendrites are neuronal structures specialized for receiving and processing information through their many synaptic inputs. How input strengths are modified across dendrites in ways that are crucial for synaptic integration and plasticity remains unclear. We examined in single hippocampal neurons the mechanism of heterosynaptic interactions and the heterogeneity of synaptic strengths of pyramidal cell inputs. Heterosynaptic presynaptic plasticity that counterbalances input strengths requires N-methyl-d-aspartate receptors (NMDARs) and astrocytes. Importantly, this mechanism is shared with the mechanism for maintaining highly heterogeneous basal presynaptic strengths, which requires astrocyte Ca(2+) signaling involving NMDAR activation, astrocyte membrane depolarization, and L-type Ca(2+) channels. Intracellular infusion of NMDARs or Ca(2+)-channel blockers into astrocytes, conditionally ablating the GluN1 NMDAR subunit, or optogenetically hyperpolarizing astrocytes with archaerhodopsin promotes homogenization of convergent presynaptic inputs. Our findings support the presence of an astrocyte-dependent cellular mechanism that enhances the heterogeneity of presynaptic strengths of convergent connections, which may help boost the computational power of dendrites.

Indexed as

Action PotentialsAnimalsAstrocytesCalcium SignalingCell CommunicationHippocampusMembrane PotentialsMiceMice, Inbred C57BLNerve NetPresynaptic TerminalsRatsSynaptic Transmissionastrocyteheterosynaptic plasticityhippocampal neuronsynapse heterogeneitysynaptic strength

Identifiers

PMID27118849
PMCPMC4868440
OpenAlexW2343739845

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.