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紫外线发光二极管照射可抑制人角质形成细胞中肿瘤坏死因子-α和干扰素-γ诱导的细胞间黏附分子-1表达及信号转导和转录激活因子1磷酸化。

Ultraviolet light-emitting-diode irradiation inhibits TNF-α and IFN-γ-induced expression of ICAM-1 and STAT1 phosphorylation in human keratinocytes.

作者信息

Kwon Tae-Rin, Oh Chang Taek, Choi Eun Ja, Kim Soon Re, Jang Yu-Jin, Ko Eun Jung, Suh Daewoong, Yoo Kwang Ho, Kim Beom Joon

机构信息

Department of Medicine, Graduate, School, Chung-Ang, University, Seoul, Korea.

Department of Dermatology, Chung-Ang, University, College of Medicine, Seoul, Korea.

出版信息

Lasers Surg Med. 2015 Dec;47(10):824-32. doi: 10.1002/lsm.22425. Epub 2015 Sep 28.

DOI:10.1002/lsm.22425
PMID:26413796
Abstract

BACKGROUND AND OBJECTIVES

Ultraviolet light-emitting diodes (UV-LEDs) are a novel light source for phototherapy. This research investigated the in vitro safety and efficacy of UV-LEDs as a phototherapeutic device for atopic dermatitis (AD).

STUDY DESIGN/MATERIALS AND METHODS: Human keratinocytes and fibroblasts were irradiated by UV-LEDs with a center wavelength of 310 and 340 nm. We examined the effects of UV-LED irradiation on the suppression of TNF-α/IFN-γ-induced activation of STAT1 and ICAM-1 and on NF-κB expression; we used the following methods: cell viability assay, reverse transcription-polymerase chain reaction, enzyme-linked immunosorbent assay, Western blotting, and immunocytochemistry.

RESULTS

We observed anti-inflammatory responses through the suppression of TNF-α/IFN-γ-induced expression of TARC and MCP-1/CCL2, IL-1beta, IL-6, and sICAM-1 via blockage of ICAM-1 activation and subsequent activation of STAT1 and NF-κB. The results suggested that UV-LED irradiation inhibited ICAM expression by suppressing TNF-α/IFN-γ-induced NF-κB activation in vitro.

CONCLUSION

We concluded that novel UV-LED (310 and 340 nm) modalities were effective for the treatment of AD and may be promising for the treatment of inflammatory skin diseases.

摘要

背景与目的

紫外线发光二极管(UV-LED)是一种用于光疗的新型光源。本研究调查了UV-LED作为特应性皮炎(AD)光疗设备的体外安全性和有效性。

研究设计/材料与方法:用中心波长为310和340nm的UV-LED照射人角质形成细胞和成纤维细胞。我们通过以下方法检测了UV-LED照射对抑制TNF-α/IFN-γ诱导的STAT1和ICAM-1激活以及对NF-κB表达的影响:细胞活力测定、逆转录-聚合酶链反应、酶联免疫吸附测定、蛋白质印迹法和免疫细胞化学。

结果

我们观察到通过阻断ICAM-1激活以及随后激活STAT1和NF-κB,抑制TNF-α/IFN-γ诱导的TARC和MCP-1/CCL2、IL-1β、IL-6和sICAM-1表达,从而产生抗炎反应。结果表明,UV-LED照射在体外通过抑制TNF-α/IFN-γ诱导的NF-κB激活来抑制ICAM表达。

结论

我们得出结论,新型UV-LED(310和340nm)模式对AD治疗有效,可能有望用于治疗炎症性皮肤病。

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