Evidence map›Paper›PMID 40875511›Full record

ArticleAging cell2025

A Prominent Pro-Inflammatory Phenotype Is Observed in Replication and Stress-Induced Senescent Mast Cells.

A Ibarra-Sánchez, I Madera-Salcedo, D Esparza-Reyes, P Mendoza-Montiel, J Padilla, C González-Espinosa

Abstract read
In one paragraph

Article in Aging cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

A Ibarra-SánchezPharmacobiology Department, Center for Research and Advanced Studies (Cinvestav) of the National Polytechnic Institute (IPN), Mexico City, Mexico.ORCID 0000-0003-1195-1808
I Madera-SalcedoImmunology and Rheumatology Department, National Institute of Medical Sciences and Nutrition Salvador Zubirán, Mexico City, Mexico.ORCID 0000-0002-0741-9248
D Esparza-ReyesPharmacobiology Department, Center for Research and Advanced Studies (Cinvestav) of the National Polytechnic Institute (IPN), Mexico City, Mexico.
P Mendoza-MontielPharmacobiology Department, Center for Research and Advanced Studies (Cinvestav) of the National Polytechnic Institute (IPN), Mexico City, Mexico.
J PadillaMicrobiology and Parasitology Department, Faculty of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.
C González-EspinosaPharmacobiology Department, Center for Research and Advanced Studies (Cinvestav) of the National Polytechnic Institute (IPN), Mexico City, Mexico.ORCID 0000-0001-7332-3829

Funding

Consejo Nacional de Ciencia y Tecnología CF-2019-1564468Consejo Nacional de Ciencia y Tecnología CF-2019-51488
6 · The paper itself

Abstract

Mast cells (MC) are long-lived important immune effectors that control inflammation, allergies, and innate immunity reactions, but the expression of specific markers in replicative and stress-induced senescence in this cell type, together with its relevance in vivo, has not been described. Here, bone marrow-derived MCs (BMMC) were generated from young C57BL6/J mice and kept in culture for a long time or treated with the well-known stressor bacterial lipopolysaccharide (LPS) to promote replicative and stress-induced senescence, respectively. Changes in size, granularity, and expression of p16

Indexed as

Cellular SenescenceInflammationMast CellsStress, PhysiologicalAnimalsCell Cycle CheckpointsLipopolysaccharidesMiceMice, Inbred C57BLPhenotypeLipopolysaccharidesinflammaginginnate immunitymast cellssenescence

Identifiers

PMID40875511
PMCPMC12507405

What OpenQuestion holds

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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.