Multifunctional Skin Dermal Extracellular Matrix Enabling Skin-Relevant Bioactivity for Tissue Remodeling, Hydration, and Anti-Hyperpigmentation
Kim YH., Park S., Cho JH., Han SY., Cho SW.
Laboratory Study on Skin Aging, published in J Microbiol Biotechnol (2026) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- J Microbiol Biotechnol (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41539855
- PMCID
- PMC12828126
- DOI
- 10.4014/jmb.2601.01001
Abstract (original English)
Dermal extracellular matrix (ECM) deterioration is a central driver of skin aging, contributing to impaired elasticity, decreased moisturization, and uneven pigmentation. However, commonly used single-component ingredients and cell-derived bioactives provide limited coordinated cues and may therefore be insufficient to address these multifactorial processes. Here, we propose decellularized skin-derived ECM (skin ECM) as a multifunctional cosmetic ingredient through comparison with various existing cosmetic ingredients. Proteomic analysis shows that skin ECM retains diverse collagen subtypes along with glycoproteins and proteoglycans associated with dermal tensile properties and matrix regulation, more closely reflecting native dermal matrisome diversity than commercial collagen products. Skin ECM at an optimal concentration most effectively upregulates the expression of genes involved in ECM remodeling and hyaluronan-mediated hydration in human dermal fibroblasts. In comparative supplementation assay, skin ECM enhances fibroblast metabolic activity and induces the strongest expression of key ECM- and hydration-related genes among all tested ingredients. Interestingly, skin ECM reduces the expression of melanogenesis-related markers and melanin accumulation in melanoma cells under experimental conditions with α-melanocyte stimulating hormone treatment. Collectively, these findin
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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