The Epidermal Environment's Influence on the Dermal Environment in Response to External Stress.


Journal

Skin pharmacology and physiology
ISSN: 1660-5535
Titre abrégé: Skin Pharmacol Physiol
Pays: Switzerland
ID NLM: 101188418

Informations de publication

Date de publication:
2023
Historique:
received: 26 09 2022
accepted: 13 02 2023
medline: 2 6 2023
pubmed: 18 3 2023
entrez: 17 3 2023
Statut: ppublish

Résumé

The outermost layer of the skin, the epidermis, is directly exposed to external stress (e.g., irradiation, allergens, and chemicals). Changes in epidermal conditions/environment in response to this stress could also influence conditions of the dermis, located directly beneath the epidermis. Yet, whether/how any epidermal environment changes in response to external stress affect dermal functions has not been completely clarified. We employed ultraviolet irradiation B (UVB) (which hardly reaches the dermis) as a model of external stress. Human keratinocytes and human dermal fibroblasts were treated with UVB and conditioned medium of keratinocytes exposed to UVB (UVB-keratinocyte-M), respectively. We assessed (1) inflammatory cytokines and lipid mediators in keratinocytes; (2) matrix metalloprotease (MMP) levels and collagen degradation in fibroblasts; (3) ex vivo organ-cultured human skin was treated with UVB. MMP levels and collagen degradation were examined; (4) test whether the mixture of agent (agent cocktail) consisting of dihydroceramide, niacin amide, resveratrol, glucosyl hesperidin, and phytosterol ester that has been shown to improve skin barrier integrity can mitigate influence of UVB in skin; and (5) a pilot one-arm human clinical test to assess efficacy of formulation containing agent cocktail on stratum corneum hydration, skin elasticity, and wrinkle index. Inflammatory-cytokine and -lipid mediator production were increased in cultured keratinocytes treated with UVB, while matrix MMP-1, -3, and -9 production and collagen degradation were increased in fibroblasts incubated with UVB-keratinocyte-M. mRNA expression of COL1A1 (that codes type 1 collagen) levels was decreased in fibroblasts incubated with UVB-keratinocyte-M. The study using ex vivo organ-cultured human skin showed both MMP-1 and MMP-9 expression were increased in both epidermis and dermis and increased dermal collagen degradation following UVB irradiation. Increased MMP production and collagen degradation were attenuated by application of an agent cocktail. Finally, a pilot clinical study demonstrated that the formulation containing our agent cocktail likely has the ability to improve skin hydration, increase skin elasticity, and reduce the appearance of wrinkles. Epidermal changes in epidermal environment and conditions in response to external stress affect dermal conditions, and these negative effects of external stress on various skin layers can be pharmacologically mitigated.

Identifiants

pubmed: 36927667
pii: 000529743
doi: 10.1159/000529743
doi:

Substances chimiques

Matrix Metalloproteinase 1 EC 3.4.24.7
Collagen Type I 0
Cytokines 0
Lipids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149-159

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Masaki Yoshida (M)

Skin Physiology Laboratory, School of Bioscience and Biotechnology, Tokyo University of Technology, Tokyo, Japan.

Kyong-Oh Shin (KO)

Department of Food Science and Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon, Republic of Korea.
The Korean Institute of Nutrition, Hallym University, Chuncheon, Republic of Korea.
LaSS Lipid Institute (LLI), LaSS Inc., Chuncheon, Republic of Korea.

Sora Muraoka (S)

Skin Physiology Laboratory, School of Bioscience and Biotechnology, Tokyo University of Technology, Tokyo, Japan.

Yerim Choi (Y)

Department of Food Science and Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon, Republic of Korea.

Jae-Ho Park (JH)

Personalized Diet Research Group, Korea Food Research Institute, Jeonju, Republic of Korea.

Soo-Hyun Park (SH)

Personalized Diet Research Group, Korea Food Research Institute, Jeonju, Republic of Korea.

Jin-Taek Hwang (JT)

Personalized Diet Research Group, Korea Food Research Institute, Jeonju, Republic of Korea.
Department of Food Biotechnology, University of Science and Technology, Daejeon, Republic of Korea.

Kyungho Park (K)

Department of Food Science and Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon, Republic of Korea.

Yoshikazu Uchida (Y)

Department of Food Science and Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon, Republic of Korea.
Department of Dermatology, School of Medicine, University of California, San Francisco, California, USA.
Northern California Institute for Research and Education (NCIRE), San Francisco, California, USA.
Veterans Affairs Medical Center, San Francisco, California, USA.

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Classifications MeSH