Evidence map›Paper›PMID 41462073›Full record

ArticleScientific reports2025

Synergistic interplay between UV and urban particulate matter exposure induces melanocyte senescence and contributes to human skin aging.

Ines Martic, Lena Guerrero-Navarro, Elia Cappuccio, Amina Hassan, Brigitte Jenewein, Elsa Arcalis, Nina Hrapovic, Lene Visdal-Johnsen, Lieve Declercq, Pidder Jansen-Dürr and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 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. Cutaneous Aging in Skin of Color: A Narrative Review.American journal of clinical dermatology · 2026
    Review
  2. Review
  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

11 authors.

Ines MarticInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria. ines.martic@uibk.ac.at.
Lena Guerrero-NavarroInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Elia CappuccioInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Amina HassanInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Brigitte JeneweinInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Elsa ArcalisInstitut Für Pflanzenbiotechnologie Und Zellbiologie, University of Natural Resources and Life Sciences (BOKU), Vienna, Austria.
Nina HrapovicScientific Research and Innovation, Oriflame Cosmetics AB, Stockholm, Sweden.
Lene Visdal-JohnsenScientific Research and Innovation, Oriflame Cosmetics AB, Stockholm, Sweden.
Lieve DeclercqEuropean Innovation Center, Proya Europe, Paris, France.
Pidder Jansen-DürrInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Maria CavinatoInstitute for Biomedical Aging Research, Universität Innsbruck, Rennweg 10, 6020, Innsbruck, Austria. maria.cavinato-nascimento@uibk.ac.at.

Funding

Austrian Science Fund DOI 10.55776/FG24European Commission's Horizon 2020 Marie Sklodowska-Curie Actions 847681Tiroler Wissenschaftsförderung ZAP746010
6 · The paper itself

Abstract

Extrinsic skin aging is driven by environmental factors, including ultraviolet (UV) radiation and air pollution. While melanocytes serve as key protectors against UV-induced damage, their role in aging, particularly through the process of senescence, remains underexplored. Here, we exposed human neonatal melanocytes and ex vivo skin explants to UV (UVA + UVB), urban particulate matter (UPM), and their combination (UV + UPM) to assess the effects on melanocyte function and skin aging. We demonstrate that combined UV + UPM exposure triggers oxidative stress, mitochondrial and DNA damage, senescence, apoptosis, and modulation of melanogenesis in human neonatal melanocytes. In addition, skin explants subjected to the same treatments showed hallmark features of aging, including epidermal thinning, barrier disruption, fibrosis, and altered pigmentation. These findings highlight that melanocytes respond to environmental stress through multiple interconnected mechanisms, potentially affecting both cell survival and pigmentary function. Our model offers a useful platform to study how environmental stressors affect melanocyte function and skin biology, potentially supporting the development of future strategies targeting pigmentation disorders and environmentally driven skin aging.

Indexed as

Cellular SenescenceMelanocytesParticulate MatterSkin AgingUltraviolet RaysApoptosisDNA DamageEnvironmental ExposureHumansMelaninsOxidative StressSkinMelaninsParticulate MatterCellular senescenceEnvironmental factorsMitochondriaPigmentationSkin aging

Identifiers

PMID41462073
PMCPMC12749940

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.