Evidence map›Paper›PMID 39197170›Full record

ArticleAging2024

Proteomic and secretomic comparison of young and aged dermal fibroblasts highlights cytoskeleton as a key component during aging.

Françoise Boismal, Sandy Peltier, Sophie Ly Ka So, Guillaume Chevreux, Loïse Blondel, Kévin Serror, Niclas Setterblab, Elina Zuelgaray, David Boccara, Maurice Mimoun and 6 more

Abstract readComparative Study
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. bioRxiv : the preprint server for biology · 2025
    Article
  5. Plant-derived extracellular vesicles in facial aesthetics.Extracellular vesicles and circulating nucleic acids · 2025
    Review
  6. 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

16 authors.

Françoise BoismalINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Sandy PeltierINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Sophie Ly Ka SoINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Guillaume ChevreuxJacques-Monod Institute, Paris, France.
Loïse BlondelINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Kévin SerrorINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Niclas SetterblabTechnological Platform IRSL, Saint-Louis Hospital, Paris, France.
Elina ZuelgarayDermatology Department, Saint-Louis Hospital, Paris, France.
David BoccaraINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Maurice MimounINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Christelle GuereClarins Laboratories, Pontoise, France.
Armand BenssussanINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.
Marie DorrClarins Laboratories, Pontoise, France.
Gallic BeauchefClarins Laboratories, Pontoise, France.
Katell VieClarins Laboratories, Pontoise, France.
Laurence MichelINSERM UMR_S 976, Skin Research Center, Saint-Louis Hospital, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crucial for skin homeostasis, synthesis and degradation of extracellular matrix components are orchestrated by dermal fibroblasts. During aging, alterations of component expression, such as collagens and enzymes, lead to reduction of the mechanical cutaneous tension and defects of skin wound healing. The aim of this study was to better understand the molecular alterations underwent by fibroblasts during aging by comparing secretomic and proteomic signatures of fibroblasts from young (<35years) and aged (>55years) skin donors, in quiescence or TGF-stimulated conditions, using HLPC/MS. The comparison of the secretome from young and aged fibroblasts revealed that 16 proteins in resting condition, and 11 proteins after a 24h-lasting TGF-β1-treatment, were expressed in significant different ways between the two cell groups (fold change>2,

Indexed as

AgingCytoskeletonFibroblastsProteomicsAdultAgedCells, CulturedDermisFemaleHumansMaleMiddle AgedProteomeSecretomeSkinTransforming Growth Factor beta1ProteomeTransforming Growth Factor beta1agingcytoskeletondermal fibroblastsproteome/secretomewound healing

Identifiers

PMID39197170
PMCPMC11386920

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.