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DNA损伤是紫外线B辐射诱导人类基因表达抑制的介导因素的证据:紫外线B辐射对细胞间黏附分子-1(ICAM-1)表达的影响。

Evidence that DNA damage is a mediate in ultraviolet B radiation-induced inhibition of human gene expression: ultraviolet B radiation effects on intercellular adhesion molecule-1 (ICAM-1) expression.

作者信息

Krutmann J, Bohnert E, Jung E G

机构信息

Department of Dermatology, University of Freiburg, Germany.

出版信息

J Invest Dermatol. 1994 Apr;102(4):428-32. doi: 10.1111/1523-1747.ep12372947.

Abstract

Expression of intercellular adhesion molecule-1 (ICAM-1) is a prerequisite for the capacity of cells to physically interact with leukocytes. Ultraviolet B radiation previously was found to inhibit interferon gamma-induced ICAM-1 expression in human keratinocytes by suppressing interferon gamma-mediated upregulation of ICAM-1 mRNA levels. Because ultraviolet B radiation induces photoproducts in cellular DNA, the potential role of ultraviolet B radiation-induced DNA damage in this system was assessed. For this purpose, cells from a normal donor were compared with cells from patients with xeroderma pigmentosum from complementation groups C and D. Xeroderma pigmentosum cells are defective in the removal of ultraviolet B radiation-induced DNA lesions, and thus lower ultraviolet B radiation doses are required to retain equivalent numbers of DNA photoproducts at a given time point after irradiation. In the present study, ultraviolet B radiation inhibited interferon gamma-induced ICAM-1 mRNA expression in primary human skin fibroblasts in a manner identical to that previously observed for keratinocytes. Comparative studies employing normal versus xeroderma pigmentosum fibroblasts revealed that in xeroderma pigmentosum fibroblasts, two- to threefold lower ultraviolet B radiation doses were required to achieve inhibition equivalent to that observed in normal fibroblasts. In irradiated normal cells, inhibition of interferon gamma-induced ICAM-1 mRNA expression was transient and restored 12 h after ultraviolet B radiation exposure. In contrast, in xeroderma pigmentosum complementation group D cells, no restoration could be observed for up to 48 h, but responsiveness was restored in xeroderma pigmentosum complementation group C cells after 24 h. These studies indicate that ultraviolet B radiation-induced inhibition of interferon gamma-mediated ICAM-1 expression involves the generation of DNA photo-products.

摘要

细胞间黏附分子-1(ICAM-1)的表达是细胞与白细胞进行物理相互作用的能力的前提条件。先前发现紫外线B辐射可通过抑制干扰素γ介导的ICAM-1 mRNA水平上调,来抑制人角质形成细胞中干扰素γ诱导的ICAM-1表达。由于紫外线B辐射会在细胞DNA中诱导光产物,因此评估了紫外线B辐射诱导的DNA损伤在该系统中的潜在作用。为此,将来自正常供体的细胞与来自C组和D组着色性干皮病患者的细胞进行了比较。着色性干皮病细胞在去除紫外线B辐射诱导的DNA损伤方面存在缺陷,因此在照射后的给定时间点,需要较低的紫外线B辐射剂量来保留等量的DNA光产物。在本研究中,紫外线B辐射以与先前在角质形成细胞中观察到的方式相同的方式抑制了原代人皮肤成纤维细胞中干扰素γ诱导的ICAM-1 mRNA表达。使用正常成纤维细胞与着色性干皮病成纤维细胞的比较研究表明,在着色性干皮病成纤维细胞中,需要低两到三倍的紫外线B辐射剂量才能达到与正常成纤维细胞中观察到的抑制效果相当的水平。在受照射的正常细胞中,干扰素γ诱导的ICAM-1 mRNA表达的抑制是短暂的,并且在紫外线B辐射暴露后12小时恢复。相比之下,在着色性干皮病D组互补细胞中,长达48小时都未观察到恢复,但在24小时后,着色性干皮病C组互补细胞的反应性恢复。这些研究表明,紫外线B辐射诱导的对干扰素γ介导的ICAM-1表达的抑制涉及DNA光产物的产生。

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