Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation

Ultraviolet B (UVB) exposure activates various inflammatory molecules of keratinocytes in the epidermis layer. Such UVB-mediated skin inflammation leaves post-inflammatory hyperpigmentation (PIH). Reports show a close relationship between PIH and high-mobility group box 1 (HMGB1) and its receptors....

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Main Authors: Hyoung Moon Kim, Seyeon Oh, Jung Hyun Yoon, Donghwan Kang, Myeongjoo Son, Kyunghee Byun
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/5/1297
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author Hyoung Moon Kim
Seyeon Oh
Jung Hyun Yoon
Donghwan Kang
Myeongjoo Son
Kyunghee Byun
author_facet Hyoung Moon Kim
Seyeon Oh
Jung Hyun Yoon
Donghwan Kang
Myeongjoo Son
Kyunghee Byun
author_sort Hyoung Moon Kim
collection DOAJ
description Ultraviolet B (UVB) exposure activates various inflammatory molecules of keratinocytes in the epidermis layer. Such UVB-mediated skin inflammation leaves post-inflammatory hyperpigmentation (PIH). Reports show a close relationship between PIH and high-mobility group box 1 (HMGB1) and its receptors. General clinical treatments of PIH, such as oral medication and laser treatment, have reported side effects. Recent studies reported the effects of radiofrequency (RF) irradiation on restoring dermal collagen, modulating the dermal vasculature, and thickening the basement membrane. To validate how RF regulates the inflammatory molecules from UVB-irradiated keratinocytes, we used UVB-radiated keratinocytes and macrophages, as well as animal skin. In addition, we examined two cases of RF-irradiated skin inflammatory diseases. We validated the effects of RF irradiation on keratinocytes by measuring expression levels of HMGB1, Toll-like receptors (TLRs), and other inflammatory factors. The results show that the RF modulates UVB-radiated keratinocytes to secrete fewer inflammatory factors and also modulates the expression of macrophages from HMGB1, TLRs, and inflammatory factors. RF irradiation could alleviate inflammatory skin diseases in patients. RF irradiation can regulate the macrophage indirectly through modulating the keratinocyte and inflammatory molecules of macrophages reduced in vitro and in vivo. Although the study is limited by the low number of cases, it demonstrates that RF irradiation can regulate skin inflammation in patients.
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spelling doaj.art-b701593ffbb64b23afc9c888c6ac3e632023-12-03T11:54:21ZengMDPI AGMolecules1420-30492021-02-01265129710.3390/molecules26051297Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin InflammationHyoung Moon Kim0Seyeon Oh1Jung Hyun Yoon2Donghwan Kang3Myeongjoo Son4Kyunghee Byun5Maylin Clinic, Goyang-si, Gyeonggi-do 10391, KoreaFunctional Cellular Networks Laboratory, Lee Gil Ya Cancer and Diabetes Institute, College of Medicine, Gachon University, Incheon 21999, KoreaYonseifams Clinic, Seoul 03396, KoreaJeisys Medical Inc., Seoul 08501, KoreaDepartment of Anatomy & Cell Biology, Gachon University College of Medicine, Incheon 21936, KoreaDepartment of Anatomy & Cell Biology, Gachon University College of Medicine, Incheon 21936, KoreaUltraviolet B (UVB) exposure activates various inflammatory molecules of keratinocytes in the epidermis layer. Such UVB-mediated skin inflammation leaves post-inflammatory hyperpigmentation (PIH). Reports show a close relationship between PIH and high-mobility group box 1 (HMGB1) and its receptors. General clinical treatments of PIH, such as oral medication and laser treatment, have reported side effects. Recent studies reported the effects of radiofrequency (RF) irradiation on restoring dermal collagen, modulating the dermal vasculature, and thickening the basement membrane. To validate how RF regulates the inflammatory molecules from UVB-irradiated keratinocytes, we used UVB-radiated keratinocytes and macrophages, as well as animal skin. In addition, we examined two cases of RF-irradiated skin inflammatory diseases. We validated the effects of RF irradiation on keratinocytes by measuring expression levels of HMGB1, Toll-like receptors (TLRs), and other inflammatory factors. The results show that the RF modulates UVB-radiated keratinocytes to secrete fewer inflammatory factors and also modulates the expression of macrophages from HMGB1, TLRs, and inflammatory factors. RF irradiation could alleviate inflammatory skin diseases in patients. RF irradiation can regulate the macrophage indirectly through modulating the keratinocyte and inflammatory molecules of macrophages reduced in vitro and in vivo. Although the study is limited by the low number of cases, it demonstrates that RF irradiation can regulate skin inflammation in patients.https://www.mdpi.com/1420-3049/26/5/1297skin inflammationTLRHMGB1micro needling radiofrequencyPIH
spellingShingle Hyoung Moon Kim
Seyeon Oh
Jung Hyun Yoon
Donghwan Kang
Myeongjoo Son
Kyunghee Byun
Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
Molecules
skin inflammation
TLR
HMGB1
micro needling radiofrequency
PIH
title Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
title_full Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
title_fullStr Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
title_full_unstemmed Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
title_short Radiofrequency Irradiation Attenuates High-Mobility Group Box 1 and Toll-like Receptor Activation in Ultraviolet B–Induced Skin Inflammation
title_sort radiofrequency irradiation attenuates high mobility group box 1 and toll like receptor activation in ultraviolet b induced skin inflammation
topic skin inflammation
TLR
HMGB1
micro needling radiofrequency
PIH
url https://www.mdpi.com/1420-3049/26/5/1297
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