Evidence map›Paper›PMID 39370688›Full record

ArticleAging cell2025

Mapping epidermal and dermal cellular senescence in human skin aging.

Grace T Yu, Clarisse Ganier, David B Allison, Tamara Tchkonia, Sundeep Khosla, James L Kirkland, Magnus D Lynch, Saranya P Wyles

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Cutaneous Melanoma in the Context of Aging.Medicina (Kaunas, Lithuania) · 2025
    Review
  15. Article
  16. SkinspanMayo Clinic proceedings · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. 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

8 authors.

Grace T YuMayo Clinic Medical Scientist Training Program, Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic Alix School of Medicine, Rochester, Minnesota, USA.ORCID 0000-0001-7161-0787
Clarisse GanierCentre for Gene Therapy and Regenerative Medicine, King's College London, Guy's Hospital, London, UK.
David B AllisonIndiana University School of Public Health, Bloomington, Indiana, USA.
Tamara TchkoniaDivision of Endocrinology and Metabolism, Department of Medicine, Center for Gerotherapeutics, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Sundeep KhoslaDivision of Endocrinology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-2936-4372
James L KirklandDivision of Endocrinology and Metabolism, Department of Medicine, Center for Gerotherapeutics, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Magnus D LynchCentre for Gene Therapy and Regenerative Medicine, King's College London, Guy's Hospital, London, UK.
Saranya P WylesRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.

Funding

Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
Midwest Murine-Tissue Mapping Center (MM-TMC)U54AG079754 · NIA · UNIVERSITY OF MINNESOTA · PI GR Scott Budinger, Sundeep Khosla · 2022 to 2026
$11.5M
Sex hormones and arthritis in a long lived animal modelP30AG050886 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Jianhua Zhang · 2015 to 2026
$11.3M
Translational Geroscience NetworkR33AG061456 · NIA · MAYO CLINIC ROCHESTER · PI JAMES L. KIRKLAND, STEPHEN B. KRITCHEVSKY · 2019 to 2026
$6.2M
Nathan Shock Centers Coordinating CenterU24AG056053 · NIA · AMERICAN FEDERATION FOR AGING RESEARCH · PI STEVEN N. AUSTAD, Stephanie Lederman · 2017 to 2026
$6.1M
Medical Scientist Traning Program at Mayo ClinicT32GM065841 · NIGMS · MAYO CLINIC ROCHESTER · PI KAUFMANN, SCOTT H, SCHIMMENTI, LISA A · 2003 to 2022
$5.8M
Defining the interactions of senescent immune cells and skeletal cellsR01AG076515 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, David G Monroe · 2022 to 2026
$2.4M
Topical Senolytics for Chronic Wound HealingR03AG082919 · NIA · MAYO CLINIC ROCHESTER · PI WYLES, SARANYA PURUSHOTHAMAN · 2023 to 2023
$323k
Gordon and Betty Moore FoundationHevolution FoundationNational Cattlemen's Beef AssociationNational Pork BoardNIA NIH HHS P01 AG062413NIA NIH HHS P30 AG050886NIA NIH HHS R01 AG076515NIA NIH HHS R03 AG082919NIA NIH HHS R33 AG061456NIA NIH HHS U24 AG056053NIA NIH HHS U54 AG079754NIGMS NIH HHS T32 GM065841NIH HHS P01AG062413NIH HHS P30AG050886NIH HHS R01AG076515NIH HHS R03AG082919-01NIH HHS R33AG061456NIH HHS R37AG013825NIH HHS T32GM065841NIH HHS U24AG056053NIH HHS U54AG079754Noaber FoundationNovo Nordisk FondenPfizer, Incthe Connor FundWeight WatchersWellcome TrustWellcome Trust 096540/Z/11/ZWellcome Trust 211276/E/18/Z
6 · The paper itself

Abstract

Single-cell RNA sequencing and spatial transcriptomics enable unprecedented insight into cellular and molecular pathways implicated in human skin aging and regeneration. Senescent cells are individual cells that are irreversibly cell cycle arrested and can accumulate across the human lifespan due to cell-intrinsic and -extrinsic stressors. With an atlas of single-cell RNA-sequencing and spatial transcriptomics, epidermal and dermal senescence and its effects were investigated, with a focus on melanocytes and fibroblasts. Photoaging due to ultraviolet light exposure was associated with higher burdens of senescent cells, a sign of biological aging, compared to chronological aging. A skin-specific cellular senescence gene set, termed SenSkin™, was curated and confirmed to be elevated in the context of photoaging, chronological aging, and non-replicating CDKN1A+ (p21) cells. In the epidermis, senescent melanocytes were associated with elevated melanin synthesis, suggesting haphazard pigmentation, while in the dermis, senescent reticular dermal fibroblasts were associated with decreased collagen and elastic fiber synthesis. Spatial analysis revealed the tendency for senescent cells to cluster, particularly in photoaged skin. This work proposes a strategy for characterizing age-related skin dysfunction through the lens of cellular senescence and suggests a role for senescent epidermal cells (i.e., melanocytes) and senescent dermal cells (i.e., reticular dermal fibroblasts) in age-related skin sequelae.

Indexed as

Cellular SenescenceSkin AgingAdultDermisEpidermisFibroblastsHumansMelanocytesUltraviolet Rayscellular senescencedermisepidermissingle‐cell gene expression analysisskin agingskin pathologyspatial analysis

Identifiers

PMID39370688
PMCPMC11709101

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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.