Evidence map›Paper›PMID 26541819›Full record

ArticleBrain, behavior, and immunity2016

Microglia regulate hippocampal neurogenesis during chronic neurodegeneration.

Chiara De Lucia, Adeline Rinchon, Adrian Olmos-Alonso, Kristoffer Riecken, Boris Fehse, Delphine Boche, V Hugh Perry, Diego Gomez-Nicola

Open access · hybridAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
4.5field-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

68 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
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  9. Review
  10. CNS Resident Innate Immune Cells: Guardians of CNS Homeostasis.International journal of molecular sciences · 2024
    Review
  11. Microglial Transforming Growth Factor-β Signaling in Alzheimer's Disease.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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  19. Review
  20. Article

8 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

8 authors at 3 institutions in 2 countries.

Chiara De LuciaCentre for Biological Sciences, University of Southampton, Southampton, United Kingdom.
Adeline RinchonCentre for Biological Sciences, University of Southampton, Southampton, United Kingdom.
Adrian Olmos-AlonsoCentre for Biological Sciences, University of Southampton, Southampton, United Kingdom.
Kristoffer RieckenResearch Department Cell and Gene Therapy, Clinic for Stem Cell Transplantation, University Medical Centre (UMC) Hamburg-Eppendorf, Hamburg, Germany.
Boris FehseResearch Department Cell and Gene Therapy, Clinic for Stem Cell Transplantation, University Medical Centre (UMC) Hamburg-Eppendorf, Hamburg, Germany.
Delphine BocheClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
V Hugh PerryCentre for Biological Sciences, University of Southampton, Southampton, United Kingdom.
Diego Gomez-NicolaCentre for Biological Sciences, University of Southampton, Southampton, United Kingdom. Electronic address: d.gomez-nicola@soton.ac.uk.
NIHR Southampton Biomedical Research Centre · GBUniversität Hamburg · DEUniversity of Southampton · GB

Funding

Medical Research Council MR/K022687/1
6 · The paper itself

Abstract

Neurogenesis is altered in neurodegenerative disorders, partly regulated by inflammatory factors. We have investigated whether microglia, the innate immune brain cells, regulate hippocampal neurogenesis in neurodegeneration. Using the ME7 model of prion disease we applied gain- or loss-of CSF1R function, as means to stimulate or inhibit microglial proliferation, respectively, to dissect the contribution of these cells to neurogenesis. We found that increased hippocampal neurogenesis correlates with the expansion of the microglia population. The selective inhibition of microglial proliferation caused a reduction in neurogenesis and a restoration of normal neuronal differentiation, supporting a pro-neurogenic role for microglia. Using a gene screening strategy, we identified TGFβ as a molecule controlling the microglial pro-neurogenic response in chronic neurodegeneration, supported by loss-of-function mechanistic experiments. By the selective targeting of microglial proliferation we have been able to uncover a pro-neurogenic role for microglia in chronic neurodegeneration, suggesting promising therapeutic targets to normalise the neurogenic niche during neurodegeneration.

Indexed as

AnimalsDisease Models, AnimalHippocampusMiceMice, Inbred C57BLMicrogliaNeurogenesisPrion DiseasesReceptors, Granulocyte-Macrophage Colony-Stimulating FactorTransforming Growth Factor betaCsf1r protein, mouseReceptors, Granulocyte-Macrophage Colony-Stimulating FactorTransforming Growth Factor betaCSF1RDentate gyrusGW2580ME7TGFb

Identifiers

PMID26541819
PMCPMC4907582
OpenAlexW2119211366

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.