Publication: Increased permeability of reconstructed human epidermis from UVB-irradiated keratinocytes
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Issued Date
2017
Resource Type
File Type
application/pdf
ISSN
9396411
Other identifier(s)
2-s2.0-85008473077
Rights Holder(s)
มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
European Journal of Pharmaceutics and Biopharmaceutics. Vol 116, (2017), p.149-154
Suggested Citation
Löwenau L.J., Zoschke C., Brodwolf R., Volz P., Hausmann C., Wattanapitayakul S., Boreham A., Alexiev U., Schäfer-Korting M. Increased permeability of reconstructed human epidermis from UVB-irradiated keratinocytes. European Journal of Pharmaceutics and Biopharmaceutics. Vol 116, (2017), p.149-154. doi:10.1016/j.ejpb.2016.12.017 Retrieved from: https://hdl.handle.net/20.500.14740/4138
Abstract
Extrinsic (photo) aging accelerates chronologically aging in the skin due to cumulative UV irradiation. Despite recent insights into the molecular mechanisms of fibroblast aging, age-related changes of the skin barrier function have been understudied. In contrast, the constantly increasing subpopulation of aged patients causes a clinical need for effective and safe (dermatological) treatment. Herein, we reconstructed human epidermis from UVB-irradiated keratinocytes (UVB-RHE). UVB-irradiated keratinocytes show higher activity of senescence associated β-galactosidase, less cell proliferation, and reduced viability. Higher amounts of β-galactosidase are also detectable in UVB-RHE. Moreover, UVB-RHE release more interleukin-1α and -8 into the culture medium and present altered differentiation with a thinner stratum corneum compared to normal RHE. For the first time, the permeation of testosterone and caffeine through UVB-irradiated RHE indicate a clear influence of the UVB stress on the skin barrier function. Impaired barrier function was confirmed by the increased permeation of testosterone and caffeine as well as by the increased penetration of dendritic core-multishell nanocarriers into the constructs. Taken together, UVB-RHE emulate hallmarks of skin aging and might contribute to an improved non-clinical development of medicinal or cosmetic products. © 2016
Subject(s)
Beta galactosidase
Caffeine
Interleukin 1alpha
Interleukin 8
Nanocarrier
Testosterone
Beta galactosidase
Caffeine
Drug carrier
Interleukin 1alpha
Interleukin 8
Nanoparticle
Testosterone
Aging
Article
Cell differentiation
Cell proliferation
Cell viability
Controlled study
Culture medium
Human
Human cell
Keratinocyte
Normal human
Permeability
Senescence
Skin permeability
Stratum corneum
Ultraviolet B radiation
Cell culture
Cell survival
Cutaneous parameters
Drug effects
Epidermis
Fibroblast
Keratinocyte
Metabolism
Physiology
Ultraviolet radiation
Beta-Galactosidase
Caffeine
Cell Differentiation
Cell Proliferation
Cell Survival
Cells, Cultured
Drug Carriers
Epidermis
Fibroblasts
Humans
Interleukin-1alpha
Interleukin-8
Keratinocytes
Nanoparticles
Permeability
Skin Aging
Testosterone
Ultraviolet Rays
Caffeine
Interleukin 1alpha
Interleukin 8
Nanocarrier
Testosterone
Beta galactosidase
Caffeine
Drug carrier
Interleukin 1alpha
Interleukin 8
Nanoparticle
Testosterone
Aging
Article
Cell differentiation
Cell proliferation
Cell viability
Controlled study
Culture medium
Human
Human cell
Keratinocyte
Normal human
Permeability
Senescence
Skin permeability
Stratum corneum
Ultraviolet B radiation
Cell culture
Cell survival
Cutaneous parameters
Drug effects
Epidermis
Fibroblast
Keratinocyte
Metabolism
Physiology
Ultraviolet radiation
Beta-Galactosidase
Caffeine
Cell Differentiation
Cell Proliferation
Cell Survival
Cells, Cultured
Drug Carriers
Epidermis
Fibroblasts
Humans
Interleukin-1alpha
Interleukin-8
Keratinocytes
Nanoparticles
Permeability
Skin Aging
Testosterone
Ultraviolet Rays
