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大鼠眼部紫外线照射后眼组织中原癌基因表达和细胞死亡的差异诱导。

Differential induction of proto-oncogene expression and cell death in ocular tissues following ultraviolet irradiation of the rat eye.

作者信息

Wickert H, Zaar K, Grauer A, John M, Zimmermann M, Gillardon F

机构信息

Department of Electron Microscopy, University of Würzburg, Germany.

出版信息

Br J Ophthalmol. 1999 Feb;83(2):225-30. doi: 10.1136/bjo.83.2.225.

Abstract

BACKGROUND/AIMS: Ultraviolet (UV) irradiation of mammalian cells in culture evokes the transcriptional activation of different proto-oncogenes, among them members of the fos/jun family which are known to play an important role in cell proliferation and differentiation. To investigate in vivo UV induced proto-oncogene expression of irradiated ocular cells, the expression of JunB, JunD, and Egr-1 was analysed in the cornea, lens, and retina. Furthermore, UV radiation is known to induce pleiotrophic events in irradiated cells which include growth arrest, inflammation, and even cell death. In order to determine the type of cell death--for example, apoptosis versus necrosis, sections of UV irradiated rat eyes were further examined for distinct ultrastructural morphology of cell death and DNA fragmentation.

METHODS

Eyes of anaesthetised rats were exposed to 1.5 J/cm2 of ultraviolet radiation (280-380 nm). Animals were perfused 6 and 16 hours after irradiation and tissue sections of enucleated bulbi were processed for light and electron microscopy.

RESULTS

Under control conditions, Jun B was constitutively expressed in numerous superficial cells but also in scattered basal cells of the corneal epithelium. After UV exposure JunB expression was massively upregulated in many cells of the basal cell layers of the corneal epithelium, although during the entire experiment, both the corneal stroma and endothelium were JunB negative. In contrast, Egr-1 was expressed exclusively in lens epithelium showing only a faint expression pattern under control conditions. However, Egr-1 expression increased after UV exposure, so that many Egr-1 positive cells of the lens epithelium could be found several hours after UV illumination. JunD was expressed in single cells of both the ganglion cell layer and the inner nuclear layer of the retina, a pattern of expression which did not change after UV exposure. Regarding the type of cell death, features of apoptosis were only occasionally present in scattered superficial cells of the corneal epithelium of control eyes. After UV exposure, however, morphological signs of apoptosis and TUNEL positive cells were visible both in the stroma and epithelium of the rat cornea. In contrast, UV irradiated lens epithelial cells exhibited features typical of necrosis. The corneal endothelium and the retina did not show any indications of morphological changes indicative of cell death after UV irradiation.

CONCLUSION

Each proto-oncogene encoded protein was found to be expressed in a tissue specific manner and UV irradiation differentially modulates the expression pattern of these transcriptional regulatory proteins. This temporospatial expression pattern of these proteins is accompanied by two morphologically distinct types of cell death in the cornea and lens after UV irradiation.

摘要

背景/目的:对培养的哺乳动物细胞进行紫外线(UV)照射可引发不同原癌基因的转录激活,其中fos/jun家族成员在细胞增殖和分化中起重要作用。为了研究体内UV诱导的受照眼细胞原癌基因表达情况,分析了角膜、晶状体和视网膜中JunB、JunD和Egr-1的表达。此外,已知UV辐射可在受照细胞中诱导多效性事件,包括生长停滞、炎症甚至细胞死亡。为了确定细胞死亡类型,例如凋亡与坏死,对UV照射的大鼠眼切片进一步检查细胞死亡的独特超微结构形态和DNA片段化情况。

方法

将麻醉大鼠的眼睛暴露于1.5 J/cm²的紫外线辐射(280 - 380 nm)。在照射后6小时和16小时对动物进行灌注,将摘除眼球的组织切片进行光镜和电镜处理。

结果

在对照条件下,Jun B在角膜上皮的许多表层细胞以及散在的基底细胞中组成性表达。UV照射后,角膜上皮基底细胞层的许多细胞中JunB表达大量上调,尽管在整个实验过程中,角膜基质和内皮均为JunB阴性。相比之下,Egr-1仅在晶状体上皮中表达,在对照条件下仅显示微弱的表达模式。然而,UV照射后Egr-1表达增加,因此在UV照射数小时后可发现晶状体上皮中有许多Egr-1阳性细胞。JunD在视网膜神经节细胞层和内核层的单个细胞中表达,这种表达模式在UV照射后没有改变。关于细胞死亡类型,对照眼角膜上皮散在的表层细胞中偶尔出现凋亡特征。然而,UV照射后,大鼠角膜基质和上皮中均可见凋亡的形态学迹象和TUNEL阳性细胞。相比之下,UV照射的晶状体上皮细胞表现出典型的坏死特征。角膜内皮和视网膜在UV照射后未显示任何表明细胞死亡的形态学变化迹象。

结论

发现每种原癌基因编码的蛋白质以组织特异性方式表达,UV照射可不同程度地调节这些转录调节蛋白的表达模式。这些蛋白质的这种时空表达模式伴随着UV照射后角膜和晶状体中两种形态学上不同的细胞死亡类型。

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EMBO J. 1997 Apr 1;16(7):1695-709. doi: 10.1093/emboj/16.7.1695.

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