Evidence map›Paper›PMID 40708474›Full record

ArticleInternational journal of cosmetic science2026

Galactomyces ferment filtrate upregulates anchoring junctions and stabilizes actin to maintain the Young's modulus of skin cells in vitro.

Steph Crabtree, Bradley B Jarrold, Olivia Kent, Matthew C Ehrman, Timothy J Hawkins, Viktor Korolchuk, Camila Pereira Braga, John M Snowball, Makio Tamura, Tomohiro Hakozaki and 3 more

Abstract read
In one paragraph

Article in International journal of cosmetic science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Steph CrabtreeNewcastle University, Newcastle, UK.
Bradley B JarroldThe Procter and Gamble Company, Cincinnati, Ohio, USA.
Olivia KentDurham University, Durham, UK.
Matthew C EhrmanProcter and Gamble International Operations (SA), Singapore, Singapore.
Timothy J HawkinsDurham University, Durham, UK.
Viktor KorolchukNewcastle University, Newcastle, UK.ORCID https://orcid.org/0000-0002-4071-592X
Camila Pereira BragaThe Procter and Gamble Company, Cincinnati, Ohio, USA.
John M SnowballThe Procter and Gamble Company, Cincinnati, Ohio, USA.
Makio TamuraThe Procter and Gamble Company, Cincinnati, Ohio, USA.
Tomohiro HakozakiThe Procter and Gamble Company, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0001-8882-1863
Akira MatsubaraProcter and Gamble, Kobe, Japan.ORCID https://orcid.org/0000-0003-3999-7517
John E OblongThe Procter and Gamble Company, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0001-7628-6242
Max BrownThe Procter and Gamble Company, Cincinnati, Ohio, USA.ORCID https://orcid.org/0009-0009-2454-7098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSkin is exposed to multiple external factors such as solar radiation and environmental oxidative stressors. Ageing and the accumulation of stress damage lead to reduced skin health and loss of skin firmness, which contribute to wrinkling and sagging. We investigated if Galactomyces ferment filtrate (GFF) could modulate skin cell mechanical properties through changes to the actin cytoskeleton and anchoring junctions.

methodsProteomic analysis was performed to identify age-associated changes in cellular components in skin biopsies and GFF-mediated changes in full thickness 3D skin equivalent models. Nanoindentation was used to measure the Young's modulus (resistance to elastic deformation) of keratinocyte cells under Latrunculin B (LatB)-induced destabilization of the actin cytoskeleton. Immunofluorescence and confocal microscopy were performed on skin equivalents to validate the GFF-induced changes observed in proteomic analysis and identify expression profiles of key structural proteins within the skin.

resultsAged skin had decreased expression of internal cellular components 'actin cytoskeleton' and 'focal adhesion'. Destabilization of actin cytoskeleton by LatB significantly reduced the Young's modulus of keratinocyte cells. Pre-treatment of keratinocytes with GFF was able to prevent LatB-induced decline of skin cell mechanical properties. Proteomic analysis of full thickness 3D skin equivalent models revealed that GFF increased the expression of 'actin cytoskeleton' and 'anchoring junctions', especially the actin-binding focal adhesion proteins. Immunofluorescence staining confirmed that GFF upregulated expression of the actin stabilizer, calponin 2 and integrin α2 in basal keratinocytes. GFF increased integrin localisation to the dermal-epidermal junction (DEJ) and colocalised with collagen IV in vitro, suggesting increased linkage between the epidermis and dermis.

conclusionOur data establish the actin cytoskeleton and anchoring junctions which bind it as important cellular structures which decline with age. We also identified that the cellular structures are required for the maintenance of keratinocyte Young's modulus, which could be an important property impacting skin firmness. Furthermore, we have identified that GFF promotes actin stability and builds a rigid holding structure of the anchoring junctions to increase cell-cell and epidermis-dermis anchoring in skin equivalent models. Therefore, GFF has the potential to help maintain and restore skin firmness in young and old skin, respectively.

Indexed as

ActinsElastic ModulusFermentationSkinHumansKeratinocytesProteomicsThiazolidinesUp-RegulationActinsThiazolidinesactin cytoskeletonanchoring junctioncalponincell adhesionepidermisintegrinkeratinocytes

Identifiers

PMID40708474
PMCPMC12877982

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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.