Evidence map›Paper›PMID 39438481›Full record

Articlenpj aging2024

Aging and senescent fates of oligodendrocyte precursor cells in the mouse brain.

Paul T Gomez, Chase M Carver, Sonia L Rodriguez, Liguo Wang, Xu Zhang, Marissa J Schafer

Abstract read
In one paragraph

Article in npj aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
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  10. Article
  11. Review
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  13. Glial Cells and Aging: From the CNS to the Cerebellum.International journal of molecular sciences · 2025
    Review
  14. Senescent brain cell types in Alzheimer's disease: Pathological mechanisms and therapeutic opportunities.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  15. Review
  16. Review
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

6 authors.

Paul T GomezRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Chase M CarverRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Sonia L RodriguezRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Liguo WangDivision of Computational Biology, Mayo Clinic College of Medicine, Rochester, MN, USA.
Xu ZhangRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-9784-0481
Marissa J SchaferRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA. schafer.marissa@mayo.edu.ORCID http://orcid.org/0000-0002-1470-1583

Funding

Spatially-resolved protein and transcriptome mapping of senescent cells (2026 SenNet Admin Supplement)UH3CA275669 · NCI · MAYO CLINIC ROCHESTER · PI Marissa Joy Schafer · 2024 to 2026
$2.3M
Spatially-resolved protein and transcriptome mapping of senescent cellsUG3CA275669 · NCI · MAYO CLINIC ROCHESTER · PI SCHAFER, MARISSA JOY · 2022 to 2023
$950k
Senescent Vascular Cells as Mediators of Cognitive DeclineR00AG058798 · NIA · MAYO CLINIC ROCHESTER · PI SCHAFER, MARISSA JOY · 2021 to 2023
$747k
Senescent Vascular Cells as Mediators of Cognitive DeclineK99AG058798 · NIA · MAYO CLINIC ROCHESTER · PI SCHAFER, MARISSA JOY · 2019 to 2020
$249k
NCI NIH HHS UG3 CA275669NCI NIH HHS UH3 CA275669NIA NIH HHS K99 AG058798NIA NIH HHS R00 AG058798U.S. Department of Health & Human Services | National Institutes of Health (NIH) AG058798U.S. Department of Health & Human Services | National Institutes of Health (NIH) CA275669
6 · The paper itself

Abstract

Age-related changes in oligodendrocyte precursor cells (OPCs) contribute to white matter dysfunction. In aged mice, we hypothesized that myelin-dense fimbria OPCs possess niche-specific properties, compared to hippocampal OPCs. Aged fimbria OPCs were fewer, larger, and localized to neighboring microglia. We identified age-increased p16/Cdkn2a-expressing OPCs enriched for senescence-related pathways and distinct senescence signatures between hippocampus and fimbria. Aged brain OPC populations differ in microenvironment properties and responses to senescence-directed intervention.

Identifiers

PMID39438481
PMCPMC11496697

What OpenQuestion holds

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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.