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利用cDNA微阵列分析HaCaT角质形成细胞对紫外线B照射的反应基因。

Analysis of genes responding to ultraviolet B irradiation of HaCaT keratinocytes using a cDNA microarray.

作者信息

Lee K M, Lee J G, Seo E Y, Lee W H, Nam Y H, Yang J M, Kee S H, Seo Y J, Park J K, Kim C D, Lee J H

机构信息

Department of Dermatology, School of Medicine, Chungnam National University, 640 Daesa-dong, Daejeon 301-040, Korea.

出版信息

Br J Dermatol. 2005 Jan;152(1):52-9. doi: 10.1111/j.1365-2133.2005.06412.x.

Abstract

BACKGROUND

Ultraviolet (UV) B irradiation causes many important biological changes in skin, which lead to pathophysiological alterations of the homeostatic environment.

OBJECTIVES

To gain more insight into the molecular events provoked by UVB irradiation, we performed cDNA microarray analysis.

METHODS

Immortalized HaCaT keratinocytes were irradiated with a high cytotoxic dose of UVB (50 mJ cm(-2)), and total RNA was isolated. Fluorescently labelled probes were prepared by reverse transcription and were hybridized with cDNA microarray slides made using 840 cDNA clones.

RESULTS

Time-course cDNA microarray analysis revealed the global gene expression profile after UVB exposure. Of 840 genes tested, 192 genes showed changes in their expression levels at one or more of four time points. The genes were clustered into four groups according to their expression patterns in a self-organizing maps analysis. Classification of these genes into nine functional categories revealed that UVB irradiation affected several biological processes. The genes that were first upregulated and then returned to normal levels included several genes related to the inhibition of cell growth and the proteasome pathway. Conversely, the expressions of many genes involved in the cytoskeleton, signal transduction, metabolism and transcription were first downregulated or unchanged and then upregulated later, reflecting the recovery of UVB-damaged cellular activities.

CONCLUSIONS

These results demonstrate the complexity of the transcriptional profile of the UVB response, and provide a basis for the global characterization of UV-regulated gene expression.

摘要

背景

紫外线B(UVB)照射会引起皮肤许多重要的生物学变化,进而导致稳态环境的病理生理改变。

目的

为了更深入了解UVB照射引发的分子事件,我们进行了cDNA微阵列分析。

方法

用高细胞毒性剂量的UVB(50 mJ/cm²)照射永生化的HaCaT角质形成细胞,然后分离总RNA。通过逆转录制备荧光标记的探针,并与使用840个cDNA克隆制作的cDNA微阵列玻片杂交。

结果

时间进程cDNA微阵列分析揭示了UVB照射后的整体基因表达谱。在检测的840个基因中,192个基因在四个时间点中的一个或多个时间点显示出表达水平的变化。根据其在自组织图谱分析中的表达模式,这些基因被聚类为四组。将这些基因分为九个功能类别,结果显示UVB照射影响了多个生物学过程。那些先上调然后恢复到正常水平的基因包括几个与细胞生长抑制和蛋白酶体途径相关的基因。相反,许多参与细胞骨架、信号转导、代谢和转录的基因的表达先是下调或无变化,随后上调,这反映了UVB损伤的细胞活动的恢复。

结论

这些结果证明了UVB反应转录谱的复杂性,并为全面表征UV调节的基因表达提供了基础。

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