Evidence map›Paper›PMID 41549518›Full record

ArticleAging cell2026

Astrocyte Senescence Impairs Synaptogenesis due to Thrombospondin-1 Loss.

Stefano Ercoli, Lucía Casares-Crespo, Elena Juárez-Escoto, Helena Mira

Abstract read
In one paragraph

Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Stefano ErcoliInstituto de Biomedicina de Valencia (IBV), CSIC, València, Spain.
Lucía Casares-CrespoInstituto de Biomedicina de Valencia (IBV), CSIC, València, Spain.
Elena Juárez-EscotoInstituto de Biomedicina de Valencia (IBV), CSIC, València, Spain.ORCID 0000-0003-4595-5591
Helena MiraInstituto de Biomedicina de Valencia (IBV), CSIC, València, Spain.ORCID 0000-0001-8574-9544

Funding

Conselleria de Innovación, Universidades, Ciencia y Sociedad Digital, Generalitat Valenciana CIAICO/2022/74Ministerio de Ciencia e Innovación (MICINN), Spain PID2022-141707NBI00Ministerio de Ciencia, Tecnología, Conocimiento e Innovación, Chile 72200297
6 · The paper itself

Abstract

Cellular senescence is an irreversible state linked to aging that involves molecular and functional alterations. The mammalian hippocampus, a key brain region for learning and memory, is highly vulnerable to damage in age-related neurodegenerative diseases, yet the role of cellular senescence in hippocampal aging remains underexplored. Here, we report an early onset of senescence signatures in hippocampal astrocytes of the accelerated aging and frailty mouse model SAMP8. We examine how astrocyte senescence affects excitatory synapse formation, focusing on soluble signals released by astrocytes. Astrocytes isolated from SAMP8 brain and those differentiated from SAMP8 neural stem cells show senescence hallmarks (SA-β-gal, p16

Indexed as

AstrocytesCellular SenescenceNeurogenesisSynapsesThrombospondin 1AgingAnimalsHippocampusMiceThrombospondin 1agingastrocyteSAMP8senescencesynaptogenesisthrombospondin

Identifiers

PMID41549518
PMCPMC12813271

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.