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Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen

E. senticosus extract (ESE), known as antioxidant, has diverse pharmacologic effects. It is also used as an antiaging agent for the skin and phlorizin (PZ) is identified as a main ingredient. In this study, the effects of PZ on epidermal stem cells were investigated. Cultured normal human keratinocy...

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Autores principales: Choi, Hye-Ryung, Nam, Kyung-Mi, Lee, Hyun-Sun, Yang, Seung-Hye, Kim, Young-Soo, Lee, Jongsung, Date, Akira, Toyama, Kazumi, Park, Kyoung-Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799823/
https://www.ncbi.nlm.nih.gov/pubmed/27042261
http://dx.doi.org/10.1155/2016/3859721
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author Choi, Hye-Ryung
Nam, Kyung-Mi
Lee, Hyun-Sun
Yang, Seung-Hye
Kim, Young-Soo
Lee, Jongsung
Date, Akira
Toyama, Kazumi
Park, Kyoung-Chan
author_facet Choi, Hye-Ryung
Nam, Kyung-Mi
Lee, Hyun-Sun
Yang, Seung-Hye
Kim, Young-Soo
Lee, Jongsung
Date, Akira
Toyama, Kazumi
Park, Kyoung-Chan
author_sort Choi, Hye-Ryung
collection PubMed
description E. senticosus extract (ESE), known as antioxidant, has diverse pharmacologic effects. It is also used as an antiaging agent for the skin and phlorizin (PZ) is identified as a main ingredient. In this study, the effects of PZ on epidermal stem cells were investigated. Cultured normal human keratinocytes and skin equivalents are used to test whether PZ affects proliferative potential of keratinocytes and how it regulates these effects. Skin equivalents (SEs) were treated with ESE and the results showed that the epidermis became slightly thickened on addition of 0.002% ESE. The staining intensity of p63 as well as proliferating cell nuclear antigen (PCNA) is increased, and integrin α6 was upregulated. Analysis of ESE confirmed that PZ is the main ingredient. When SEs were treated with PZ, similar findings were observed. In particular, the expression of integrin α6, integrin β1, and type IV collagen was increased. Levels of mRNA for type IV collagen were increased and levels of miR135b were downregulated. All these findings suggested that PZ can affect the proliferative potential of epidermal cells in part by microenvironment changes via miR135b downregulation and following increased expression of type IV collagen.
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spelling pubmed-47998232016-04-03 Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen Choi, Hye-Ryung Nam, Kyung-Mi Lee, Hyun-Sun Yang, Seung-Hye Kim, Young-Soo Lee, Jongsung Date, Akira Toyama, Kazumi Park, Kyoung-Chan Oxid Med Cell Longev Research Article E. senticosus extract (ESE), known as antioxidant, has diverse pharmacologic effects. It is also used as an antiaging agent for the skin and phlorizin (PZ) is identified as a main ingredient. In this study, the effects of PZ on epidermal stem cells were investigated. Cultured normal human keratinocytes and skin equivalents are used to test whether PZ affects proliferative potential of keratinocytes and how it regulates these effects. Skin equivalents (SEs) were treated with ESE and the results showed that the epidermis became slightly thickened on addition of 0.002% ESE. The staining intensity of p63 as well as proliferating cell nuclear antigen (PCNA) is increased, and integrin α6 was upregulated. Analysis of ESE confirmed that PZ is the main ingredient. When SEs were treated with PZ, similar findings were observed. In particular, the expression of integrin α6, integrin β1, and type IV collagen was increased. Levels of mRNA for type IV collagen were increased and levels of miR135b were downregulated. All these findings suggested that PZ can affect the proliferative potential of epidermal cells in part by microenvironment changes via miR135b downregulation and following increased expression of type IV collagen. Hindawi Publishing Corporation 2016 2016-03-06 /pmc/articles/PMC4799823/ /pubmed/27042261 http://dx.doi.org/10.1155/2016/3859721 Text en Copyright © 2016 Hye-Ryung Choi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Choi, Hye-Ryung
Nam, Kyung-Mi
Lee, Hyun-Sun
Yang, Seung-Hye
Kim, Young-Soo
Lee, Jongsung
Date, Akira
Toyama, Kazumi
Park, Kyoung-Chan
Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title_full Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title_fullStr Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title_full_unstemmed Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title_short Phlorizin, an Active Ingredient of Eleutherococcus senticosus, Increases Proliferative Potential of Keratinocytes with Inhibition of MiR135b and Increased Expression of Type IV Collagen
title_sort phlorizin, an active ingredient of eleutherococcus senticosus, increases proliferative potential of keratinocytes with inhibition of mir135b and increased expression of type iv collagen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799823/
https://www.ncbi.nlm.nih.gov/pubmed/27042261
http://dx.doi.org/10.1155/2016/3859721
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