Evidence map›Paper›PMID 38789561›Full record

ArticleCommunications biology2024

In vivo cyclic overexpression of Yamanaka factors restricted to neurons reverses age-associated phenotypes and enhances memory performance.

Alejandro Antón-Fernández, Marta Roldán-Lázaro, Laura Vallés-Saiz, Jesús Ávila, Félix Hernández

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. A cross-talk between p16High senescence and cellular reprogramming.Clinical science (London, England : 1979) · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Personalized Stem Cell-Based Regeneration in Spinal Cord Injury Care.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Research ofRegenerative therapy · 2025
    Review
  14. 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

5 authors.

Alejandro Antón-Fernández *Centro de Biología Molecular Severo Ochoa (UAM-CSIC), Nicolás Cabrera, 1. Cantoblanco, 28049, Madrid, Spain. aanton@cbm.csic.es.ORCID 0000-0001-8029-4288
Marta Roldán-Lázaro *Centro de Biología Molecular Severo Ochoa (UAM-CSIC), Nicolás Cabrera, 1. Cantoblanco, 28049, Madrid, Spain.
Laura Vallés-SaizCentro de Biología Molecular Severo Ochoa (UAM-CSIC), Nicolás Cabrera, 1. Cantoblanco, 28049, Madrid, Spain.ORCID 0000-0002-9278-7642
Jesús ÁvilaCentro de Biología Molecular Severo Ochoa (UAM-CSIC), Nicolás Cabrera, 1. Cantoblanco, 28049, Madrid, Spain.ORCID 0000-0002-6288-0571
Félix HernándezCentro de Biología Molecular Severo Ochoa (UAM-CSIC), Nicolás Cabrera, 1. Cantoblanco, 28049, Madrid, Spain. fhernandez@cbm.csic.es.ORCID 0000-0001-8753-8249

Funding

Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) PGC-2018-09177-B-100Ministerio de Economía y Competitividad (Ministry of Economy and Competitiveness) PID2020-113204GB-I00
6 · The paper itself

Abstract

In recent years, there has been success in partially reprogramming peripheral organ cells using cyclic Yamanaka transcription factor (YF) expression, resulting in the reversal of age-related pathologies. In the case of the brain, the effects of partial reprogramming are scarcely known, and only some of its effects have been observed through the widespread expression of YF. This study is the first to exclusively partially reprogram a specific subpopulation of neurons in the cerebral cortex of aged mice. The in vivo model demonstrate that YF expression in postmitotic neurons does not dedifferentiate them, and it avoids deleterious effects observed with YF expression in other cell types. Additionally, our study demonstrates that only cyclic, not continuous, expression of YF result in a noteworthy enhancement of cognitive function in adult mice. This enhancement is closely tied to increased neuronal activation in regions related to memory processes, reversed aging-related epigenetic markers and to increased plasticity, induced by the reorganization of the extracellular matrix. These findings support the therapeutic potential of targeted partial reprogramming of neurons in addressing age-associated phenotypes and neurodegenerative diseases correlated with aging.

Indexed as

AgingMemoryNeuronsPhenotypeAnimalsCellular ReprogrammingCerebral CortexFemaleMaleMiceMice, Inbred C57BLTranscription FactorsTranscription Factors

Identifiers

PMID38789561
PMCPMC11126596

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.