Evidence map›Paper›PMID 24748560›Full record

ArticleBrain structure & function2015

Pre-existing astrocytes form functional perisynaptic processes on neurons generated in the adult hippocampus.

Marine Krzisch, Silvio G Temprana, Lucas A Mongiat, Jan Armida, Valentin Schmutz, Mari A Virtanen, Jacqueline Kocher-Braissant, Rudolf Kraftsik, Laszlo Vutskits, Karl-Klaus Conzelmann and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

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  12. Glial cells in Parkinson´s disease: protective or deleterious?Cellular and molecular life sciences : CMLS · 2020
    Review
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  19. Exercising New Neurons to Vanquish Alzheimer Disease.Brain plasticity (Amsterdam, Netherlands) · 2018
    Review
  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

14 authors at 8 institutions in 4 countries.

Marine KrzischDepartment of Fundamental Neurosciences, University of Lausanne, 9 rue du Bugnon, 1005, Lausanne, Switzerland.
Silvio G Temprana
Lucas A Mongiat
Jan Armida
Valentin Schmutz
Mari A Virtanen
Jacqueline Kocher-Braissant
Rudolf Kraftsik
Laszlo Vutskits
Karl-Klaus Conzelmann
Matteo Bergami
Fred H Gage
Alejandro F Schinder
Nicolas Toni
University of Lausanne · CHConsejo Nacional de Investigaciones Científicas y Técnicas · ARCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEFundación Instituto Leloir · ARLudwig-Maximilians-Universität München · DESalk Institute for Biological Studies · USUniversity Hospital of Geneva · CHUniversity of Geneva · CH

Funding

Role of Astrocyte-Derived Wnts in Adult NeurogenesisR01NS050217 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GAGE, FRED H · 2005 to 2009
$2.7M
Howard Hughes Medical InstituteNINDS NIH HHS NS050217NINDS NIH HHS R01 NS050217
6 · The paper itself

Abstract

The adult dentate gyrus produces new neurons that morphologically and functionally integrate into the hippocampal network. In the adult brain, most excitatory synapses are ensheathed by astrocytic perisynaptic processes that regulate synaptic structure and function. However, these processes are formed during embryonic or early postnatal development and it is unknown whether astrocytes can also ensheathe synapses of neurons born during adulthood and, if so, whether they play a role in their synaptic transmission. Here, we used a combination of serial-section immuno-electron microscopy, confocal microscopy, and electrophysiology to examine the formation of perisynaptic processes on adult-born neurons. We found that the afferent and efferent synapses of newborn neurons are ensheathed by astrocytic processes, irrespective of the age of the neurons or the size of their synapses. The quantification of gliogenesis and the distribution of astrocytic processes on synapses formed by adult-born neurons suggest that the majority of these processes are recruited from pre-existing astrocytes. Furthermore, the inhibition of astrocytic glutamate re-uptake significantly reduced postsynaptic currents and increased paired-pulse facilitation in adult-born neurons, suggesting that perisynaptic processes modulate synaptic transmission on these cells. Finally, some processes were found intercalated between newly formed dendritic spines and potential presynaptic partners, suggesting that they may also play a structural role in the connectivity of new spines. Together, these results indicate that pre-existing astrocytes remodel their processes to ensheathe synapses of adult-born neurons and participate to the functional and structural integration of these cells into the hippocampal network.

Indexed as

Aldehyde Dehydrogenase 1 FamilyAnimalsAstrocytesBromodeoxyuridineDendritic SpinesExcitatory Postsynaptic PotentialsGene Expression RegulationGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsHippocampusIsoenzymesKainic AcidMiceMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, mouseBromodeoxyuridinedihydrokainic acidGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsIsoenzymesKainic AcidPhosphopyruvate HydrataseRetinal DehydrogenaseS100 Calcium Binding Protein beta Subunit

Identifiers

PMID24748560
PMCPMC4481333
OpenAlexW2010598641

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.