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培养的肝细胞中谷胱甘肽S-转移酶的差异调节

Differential regulation of glutathione S-transferases in cultured hepatocytes.

作者信息

Abramovitz M, Ishigaki S, Listowsky I

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

Hepatology. 1989 Feb;9(2):235-9. doi: 10.1002/hep.1840090212.

Abstract

Specific cDNA probes were used to determine steady-state mRNA levels for the multiple glutathione S-transferases in primary hepatocyte cultures. In the first 24 hr of culture, gene transcripts for the Ya family decreased sharply, Yb3 disappeared completely, but changes in levels of mRNA for Yb1 and Yb2 were smaller. These results suggest that the isoenzymes are regulated independently. Yp mRNA, which is present at greatly elevated levels in hyperplastic nodules and hepatocellular carcinomas but not in normal adult livers, was hardly detectable in freshly isolated hepatocytes, but Yp transcripts rapidly accumulated in the first 24 hr in culture and continued to increase for 72 hr. Decreased levels in Ya and Yc and increases in Yp were detected by immunoblotting methods, indicating that translation products changed together with mRNA levels in the cultured cells. The appearance of Yp transcripts in hepatocytes was effectively blocked by addition of dexamethasone to the culture medium. Elevations of Yp levels are characteristic of the cell culture system and factors regulating Yp transcription in nodules and carcinomas may also be operative in cultured hepatocytes.

摘要

使用特异性cDNA探针来测定原代肝细胞培养物中多种谷胱甘肽S-转移酶的稳态mRNA水平。在培养的最初24小时内,Ya家族的基因转录本急剧下降,Yb3完全消失,但Yb1和Yb2的mRNA水平变化较小。这些结果表明,同工酶是独立调节的。Yp mRNA在增生性结节和肝细胞癌中水平大幅升高,但在正常成年肝脏中不存在,在新鲜分离的肝细胞中几乎检测不到,但Yp转录本在培养的最初24小时内迅速积累,并在72小时内持续增加。通过免疫印迹法检测到Ya和Yc水平降低以及Yp水平升高,表明翻译产物与培养细胞中的mRNA水平一起发生变化。向培养基中添加地塞米松可有效阻断肝细胞中Yp转录本的出现。Yp水平升高是细胞培养系统的特征,调节结节和癌中Yp转录的因子在培养的肝细胞中可能也起作用。

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