Evidence map›Paper›PMID 26138449›Full record

ArticleMolecular neurobiology2016

The Neurogenic Potential of Astrocytes Is Regulated by Inflammatory Signals.

Alessandro Michelucci, Angela Bithell, Matthew J Burney, Caroline E Johnston, Kee-Yew Wong, Siaw-Wei Teng, Jyaysi Desai, Nigel Gumbleton, Gregory Anderson, Lawrence W Stanton and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Role of Senescent Astrocytes in Health and Disease.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Adult neurogenesis from reprogrammed astrocytes.Neural regeneration research · 2020
    Review
  13. Article
  14. Review
  15. Generating Brain Waves, the Power of Astrocytes.Frontiers in neuroscience · 2019
    Review
  16. Article
  17. Article
  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

12 authors at 5 institutions in 3 countries.

Alessandro MichelucciInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Angela BithellSchool of Pharmacy, Department of Pharmacology, The Hopkins Building, University of Reading, Whiteknights, Reading, RG6 6AP, UK. a.bithell@reading.ac.uk.
Matthew J BurneyInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Caroline E JohnstonInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Kee-Yew WongGenome Institute of Singapore, 60 Biopolis Street, #02-01, Genome Building, Singapore, 138672, Singapore.
Siaw-Wei TengGenome Institute of Singapore, 60 Biopolis Street, #02-01, Genome Building, Singapore, 138672, Singapore.
Jyaysi DesaiInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Nigel GumbletonSchool of Pharmacy, Department of Pharmacology, The Hopkins Building, University of Reading, Whiteknights, Reading, RG6 6AP, UK.
Gregory AndersonInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Lawrence W StantonGenome Institute of Singapore, 60 Biopolis Street, #02-01, Genome Building, Singapore, 138672, Singapore.
Brenda P WilliamsInstitute of Psychiatry, Centre for the Cellular Basis of Behaviour, The James Black Centre, King's College London, 125 Coldharbour Lane, London, SE5 9NU, UK.
Noel J BuckleyDepartment of Psychiatry, Warneford Hospital, University of Oxford, Warneford Lane, Oxford, OX3 7JX, UK. noel.buckley@psych.ox.ac.uk.
King's College London · GBGenome Institute of Singapore · SGUniversity of Reading · GBUniversity of Luxembourg · LUUniversity of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Although the adult brain contains neural stem cells (NSCs) that generate new neurons throughout life, these astrocyte-like populations are restricted to two discrete niches. Despite their terminally differentiated phenotype, adult parenchymal astrocytes can re-acquire NSC-like characteristics following injury, and as such, these 'reactive' astrocytes offer an alternative source of cells for central nervous system (CNS) repair following injury or disease. At present, the mechanisms that regulate the potential of different types of astrocytes are poorly understood. We used in vitro and ex vivo astrocytes to identify candidate pathways important for regulation of astrocyte potential. Using in vitro neural progenitor cell (NPC)-derived astrocytes, we found that exposure of more lineage-restricted astrocytes to either tumor necrosis factor alpha (TNF-α) (via nuclear factor-κB (NFκB)) or the bone morphogenetic protein (BMP) inhibitor, noggin, led to re-acquisition of NPC properties accompanied by transcriptomic and epigenetic changes consistent with a more neurogenic, NPC-like state. Comparative analyses of microarray data from in vitro-derived and ex vivo postnatal parenchymal astrocytes identified several common pathways and upstream regulators associated with inflammation (including transforming growth factor (TGF)-β1 and peroxisome proliferator-activated receptor gamma (PPARγ)) and cell cycle control (including TP53) as candidate regulators of astrocyte phenotype and potential. We propose that inflammatory signalling may control the normal, progressive restriction in potential of differentiating astrocytes as well as under reactive conditions and represent future targets for therapies to harness the latent neurogenic capacity of parenchymal astrocytes.

Indexed as

NeurogenesisAnimalsAnimals, NewbornAstrocytesBone Morphogenetic Protein 4Cell DedifferentiationCell LineCell ProliferationCentral Nervous SystemEpigenesis, GeneticGene Expression ProfilingGene Expression RegulationHistonesInflammationMiceModels, BiologicalBone Morphogenetic Protein 4HistonesNF-kappa BTumor Necrosis Factor-alphaAstrocytesEpigeneticInflammationNeural stem cellsNFκBNoggin

Identifiers

PMID26138449
PMCPMC4937102
OpenAlexW1603300908

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.