Evidence map›Paper›PMID 31905199›Full record

ArticlePLoS biology2020

Neuron-glia interaction through Serotonin-BDNF-NGFR axis enables regenerative neurogenesis in Alzheimer's model of adult zebrafish brain.

Prabesh Bhattarai, Mehmet Ilyas Cosacak, Violeta Mashkaryan, Sevgican Demir, Stanislava Dimitrova Popova, Nambirajan Govindarajan, Kerstin Brandt, Yixin Zhang, Weipang Chang, Konstantinos Ampatzis and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

63 citing papers in PubMed, 107 citations in OpenAlex.

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  15. Wnt/β-catenin Signaling in Central Nervous System Regeneration.Advances in experimental medicine and biology · 2025
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  19. Insights into the genetic architecture of the reciprocal interspecific hybrids derived fromMolecular breeding : new strategies in plant improvement · 2024
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3 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 2 countries.

Prabesh BhattaraiGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.
Mehmet Ilyas CosacakGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.ORCID 0000-0003-2978-3902
Violeta MashkaryanGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.
Sevgican DemirGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.ORCID 0000-0001-8610-1192
Stanislava Dimitrova PopovaGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.
Nambirajan GovindarajanGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.
Kerstin BrandtGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.
Yixin ZhangB CUBE, Center for Molecular Bioengineering, Technische Universität Dresden, Dresden, Germany.
Weipang ChangKarolinska Institutet, Neuroscience Department, Stockholm, Sweden.
Konstantinos AmpatzisKarolinska Institutet, Neuroscience Department, Stockholm, Sweden.ORCID 0000-0001-7998-6463
Caghan KizilGerman Center for Neurodegenerative Diseases (DZNE) within Helmholtz Association, Dresden, Germany.ORCID 0000-0002-8164-9762
German Center for Neurodegenerative Diseases · DEKarolinska Institutet · SETechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It was recently suggested that supplying the brain with new neurons could counteract Alzheimer's disease (AD). This provocative idea requires further testing in experimental models in which the molecular basis of disease-induced neuronal regeneration could be investigated. We previously found that zebrafish stimulates neural stem cell (NSC) plasticity and neurogenesis in AD and could help to understand the mechanisms to be harnessed for developing new neurons in diseased mammalian brains. Here, by performing single-cell transcriptomics, we found that amyloid toxicity-induced interleukin-4 (IL4) promotes NSC proliferation and neurogenesis by suppressing the tryptophan metabolism and reducing the production of serotonin. NSC proliferation was suppressed by serotonin via down-regulation of brain-derived neurotrophic factor (BDNF)-expression in serotonin-responsive periventricular neurons. BDNF enhances NSC plasticity and neurogenesis via nerve growth factor receptor A (NGFRA)/ nuclear factor 'kappa-light-chain-enhancer' of activated B-cells (NFkB) signaling in zebrafish but not in rodents. Collectively, our results suggest a complex neuron-glia interaction that regulates regenerative neurogenesis after AD conditions in zebrafish.

Indexed as

Alzheimer DiseaseAge FactorsAnimalsAnimals, Genetically ModifiedBrainBrain-Derived Neurotrophic FactorCell CommunicationDisease Models, AnimalMaleMiceMice, TransgenicNerve RegenerationNeural Stem CellsNeurogenesisNeurogliaNeuroimmunomodulationBrain-Derived Neurotrophic FactorReceptors, Nerve Growth FactorSerotoninZebrafish Proteins

Identifiers

PMID31905199
PMCPMC6964913
OpenAlexW2997775632

What OpenQuestion holds

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LicenceCC BY
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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.