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角质形成细胞系中紫外线B诱导型一氧化氮合酶mRNA表达及一氧化氮生成的时间进程。

Time course of expression of mRNA of inducible nitric oxide synthase and generation of nitric oxide by ultraviolet B in keratinocyte cell lines.

作者信息

Seo S J, Choi H G, Chung H J, Hong C K

机构信息

Department of Dermatology, College of Medicine, Chung Ang University Hospital, 65 207, Hanganro-3-ka, Yonsan-ku, Seoul 140-757, Korea.

出版信息

Br J Dermatol. 2002 Oct;147(4):655-62. doi: 10.1046/j.1365-2133.2002.04849.x.

Abstract

BACKGROUND

Nitric oxide (NO), the ubiquitous free radical, has been implicated in the pathogenesis of various inflammatory diseases, including sunburn and ultraviolet (UV) radiation-induced pigmentation, and it also seems to play an important part in host defence against bacterial infection.

OBJECTIVES

The purpose of this study was to determine the time course of production of NO and time course of expression of inducible NO synthase (iNOS) by UVB irradiation and lipopolysaccharide (LPS) stimulation in keratinocyte cell lines. Furthermore, we intended to elucidate the relationship between iNOS and NO in various stimulated conditions.

METHODS

Normal human keratinocytes (NHK), HaCaT cells and PAM212 cells were irradiated with UVB at a dose of 50 mJ cm-2 and 100 mJ cm-2. Separately, the cell lines were stimulated with 20 micro g of LPS. NO was measured by the Griess assay and iNOS mRNA was isolated by reverse transcriptase-polymerase chain reaction at 12, 24, 48 and 72 h after stimulation.

RESULTS

The generation of NO was induced by UVB irradiation and LPS stimulation. NO production was significantly increased at 72 h after irradiation of UVB 100 mJ cm-2 in NHK, and at 48 and 72 h in HaCaT cells. In PAM212 cells, NO production was significantly increased at 12, 24, 48 and 72 h by UVB 100 mJ cm-2 and at 72 h by LPS. Induction of iNOS mRNA peaked at 48 h and then decreased to basal level at 72 h when treated with UVB irradiation. The time course of production of NO was approximately correlated with the timing of induction of iNOS mRNA.

CONCLUSIONS

These results suggest that the expression of iNOS mRNA is upregulated by UVB irradiation, and that NO produced by this inducible enzyme may play a part as a mediator or an immunomodulator in UV-induced skin reactions such as sunburn reaction and photo-induced immune alterations.

摘要

背景

一氧化氮(NO)作为一种广泛存在的自由基,与包括晒伤和紫外线(UV)辐射诱导的色素沉着在内的各种炎症性疾病的发病机制有关,并且它似乎在宿主抵御细菌感染中也起着重要作用。

目的

本研究的目的是确定角质形成细胞系中经紫外线B(UVB)照射和脂多糖(LPS)刺激后NO产生的时间进程以及诱导型一氧化氮合酶(iNOS)表达的时间进程。此外,我们旨在阐明在各种刺激条件下iNOS与NO之间的关系。

方法

正常人角质形成细胞(NHK)、HaCaT细胞和PAM212细胞分别以50 mJ/cm²和100 mJ/cm²的剂量接受UVB照射。另外,用20 μg的LPS刺激这些细胞系。在刺激后12、24、48和72小时,通过格里斯试剂法测量NO,并通过逆转录聚合酶链反应分离iNOS mRNA。

结果

UVB照射和LPS刺激均可诱导NO的产生。在NHK中,100 mJ/cm²的UVB照射后72小时NO产生显著增加,在HaCaT细胞中48和72小时显著增加。在PAM212细胞中,100 mJ/cm²的UVB照射在12、24、48和72小时可使NO产生显著增加,LPS刺激在72小时可使NO产生显著增加。用UVB照射处理时,iNOS mRNA的诱导在48小时达到峰值,然后在72小时降至基础水平。NO产生的时间进程与iNOS mRNA诱导的时间大致相关。

结论

这些结果表明,UVB照射可上调iNOS mRNA的表达,并且这种诱导酶产生的NO可能在UV诱导的皮肤反应如晒伤反应和光诱导的免疫改变中作为介质或免疫调节剂发挥作用。

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