Evidence map›Paper›PMID 31560167›Full record

ArticleAging cell2019

Neuronal p38α mediates age-associated neural stem cell exhaustion and cognitive decline.

Leire Moreno-Cugnon, Miren Revuelta, Olatz Arrizabalaga, Sandra Colie, Manuel Moreno-Valladares, Daniel Jimenez-Blasco, Francisco Gil-Bea, Irantzu Llarena, Juan Pedro Bolaños, Angel R Nebreda and 1 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Aging · 2021
    Article
  8. Opportunities and Challenges in Stem Cell Aging.Advances in experimental medicine and biology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. 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

11 authors at 7 institutions in 1 country.

Leire Moreno-CugnonCellular oncology group, Biodonostia Institute, San Sebastian, Spain.
Miren RevueltaCellular oncology group, Biodonostia Institute, San Sebastian, Spain.
Olatz ArrizabalagaCellular oncology group, Biodonostia Institute, San Sebastian, Spain.
Sandra ColieInstitute for Research in Biomedicine (IRB Barcelona), Barcelona Institute of Science and Technology, Barcelona, Spain.
Manuel Moreno-ValladaresCellular oncology group, Biodonostia Institute, San Sebastian, Spain.
Daniel Jimenez-BlascoInstitute of Functional Biology and Genomics (IBFG), Universidad de Salamanca, CSIC, Salamanca, Spain.
Francisco Gil-BeaNeurosciences Area, Biodonostia Institute, San Sebastián, Spain.
Irantzu LlarenaOptical Spectroscopy Platform, CIC biomaGUNE, San Sebastian, Spain.
Juan Pedro BolañosInstitute of Functional Biology and Genomics (IBFG), Universidad de Salamanca, CSIC, Salamanca, Spain.
Angel R NebredaInstitute for Research in Biomedicine (IRB Barcelona), Barcelona Institute of Science and Technology, Barcelona, Spain.
Ander MatheuCellular oncology group, Biodonostia Institute, San Sebastian, Spain.ORCID 0000-0002-1848-0781
Biogipuzkoa Health Research Institute · ESUniversidad de Salamanca · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESCIC biomaGUNE · ESIkerbasque · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstitute for Research in Biomedicine · ES

Funding

CIBERFES CB16/10/00282FEDER FundsInstituto de Salud Carlos III CP16/00039Instituto de Salud Carlos III PI13/02277Instituto de Salud Carlos III PI16/01580Spanish Ministry of Economy and Competitiveness (MINECO) CSD2010-0045Spanish Ministry of Economy and Competitiveness (MINECO) SAF2016-78114-R
6 · The paper itself

Abstract

Neuronal activity regulates cognition and neural stem cell (NSC) function. The molecular pathways limiting neuronal activity during aging remain largely unknown. In this work, we show that p38MAPK activity increases in neurons with age. By using mice expressing p38α-lox and CamkII-Cre alleles (p38α∆-N), we demonstrate that genetic deletion of p38α in neurons suffices to reduce age-associated elevation of p38MAPK activity, neuronal loss and cognitive decline. Moreover, aged p38α∆-N mice present elevated numbers of NSCs in the hippocampus and the subventricular zone. These results reveal novel roles for neuronal p38MAPK in age-associated NSC exhaustion and cognitive decline.

Indexed as

AgingAnimalsCognitive DysfunctionMiceMitogen-Activated Protein Kinase 14Neural Stem CellsNeuronsMitogen-Activated Protein Kinase 14agingcognitive declineneural stem cellsneuronal activityp38MAPK

Identifiers

PMID31560167
PMCPMC6826142
OpenAlexW2975848098

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.