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用溴化乙锭和吖啶橙对构巢曲霉中的细胞凋亡进行原位分析。

In situ analysis of apoptosis in Aspergillus nidulans with ethidium bromide and acridine orange.

作者信息

Leles S M, Factori R, Rocha C L M S C

机构信息

Departamento de Biotecnologia, Genética e Biologia Celular, Universidade Estadual de Maringá, Maringá, PR, Brasil.

出版信息

Genet Mol Res. 2013 Aug 12;12(3):2895-901. doi: 10.4238/2013.August.12.5.

Abstract

Apoptosis and necrosis are among several types of cell death. We stained the nuclei of Aspergillus nidulans grown in micro-colonies with ethidium bromide and acridine orange to detect in situ apoptosis. Suspensions of conidia from 5-day-old colonies of the A. nidulans strains biA1methG1, G422, CLC100, and CLB3 were each put into two tubes. The suspension of one tube was irradiated with ultraviolet light for 20 s, whereas the other tube was not exposed to irradiation. The two suspensions were inoculated in complete liquid medium and 50-µL samples were placed on sterilized cover slips, spread on the surface of solid culture media on Petri dishes. After the micro-colonies were formed, the material on the cover slips was stained with ethidium bromide and acridine orange, placed on the lamina and observed under a fluorescence microscope. This staining method was efficient in discriminating normal nuclei from those going apoptosis and necrosis. Results have shown that irradiation provokes apoptosis but does not induce necrosis. There were no differences between the three strains and all data were considered to be statistically significant.

摘要

凋亡和坏死是几种细胞死亡类型中的两种。我们用溴化乙锭和吖啶橙对在微菌落中生长的构巢曲霉细胞核进行染色,以原位检测凋亡。将构巢曲霉菌株biA1methG1、G422、CLC100和CLB3的5日龄菌落的分生孢子悬浮液分别放入两支试管中。其中一支试管的悬浮液用紫外线照射20秒,而另一支试管不进行照射。将这两种悬浮液接种到完全液体培养基中,并将50微升样品置于灭菌盖玻片上,铺展在培养皿中固体培养基的表面。在形成微菌落后,将盖玻片上的材料用溴化乙锭和吖啶橙染色,置于载玻片上并在荧光显微镜下观察。这种染色方法在区分正常细胞核与发生凋亡和坏死的细胞核方面很有效。结果表明,照射可引发凋亡但不诱导坏死。这三个菌株之间没有差异,所有数据均被认为具有统计学意义。

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