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部分肝切除术后再生大鼠肝脏中的基因表达谱

Gene expression profile in the regenerating rat liver after partial hepatectomy.

作者信息

Fukuhara Yasuyuki, Hirasawa Akira, Li Xiao Kang, Kawasaki Mikiko, Fujino Masayuki, Funeshima Naoko, Katsuma Susumu, Shiojima Satoshi, Yamada Masateru, Okuyama Torayuki, Suzuki Seiichi, Tsujimoto Gozoh

机构信息

Department of Innovative Surgery, National Research Institute for Child Health and Development, 3-35-31 Taishido, Setagaya-ku, 154-8567, Tokyo, Japan.

出版信息

J Hepatol. 2003 Jun;38(6):784-92. doi: 10.1016/s0168-8278(03)00077-1.

Abstract

BACKGROUND/AIMS: When a loss of hepatic mass occurs, the expression of a large number of genes is either induced or altered, accompanying hepatocyte proliferation. In the present study, we made an in-house cDNA microarray containing 4608 elements (Liver chip), and analyzed extensively gene expression profiles of the regenerating liver after 70% partial hepatectomy (PHx) in rats.

METHODS

RNAs were prepared from three rat livers at each time point (taken at 0, 6, 12, 18, 24, 48, 72 h, and 1 week after PHx). Using the liver chip, we performed large-scale analysis of gene expression during liver regeneration. Elements either up- or down-regulated more than twofold at one or more time points were selected.

RESULTS

Among the 4608, 382 were identified. Using cluster analysis, we found great similarity between gene-expression profiles at 12 and 18 h after PHx as well as between 48 and 72 h after PHx. We also found that there are at least six distinct temporal patterns of gene expression in the regenerating rat liver after PHx.

CONCLUSIONS

These results indicated that microarray analysis is a powerful approach for monitoring molecular events in the regenerating liver.

摘要

背景/目的:当肝组织质量减少时,伴随着肝细胞增殖,大量基因的表达会被诱导或改变。在本研究中,我们制作了一个包含4608个元件的自制cDNA微阵列(肝脏芯片),并广泛分析了大鼠70%部分肝切除(PHx)后再生肝脏的基因表达谱。

方法

在每个时间点(PHx后0、6、12、18、24、48、72小时和1周)从三只大鼠肝脏中提取RNA。使用肝脏芯片,我们对肝脏再生过程中的基因表达进行了大规模分析。选择在一个或多个时间点上调或下调超过两倍的元件。

结果

在4608个元件中,鉴定出382个。通过聚类分析,我们发现PHx后12小时和18小时以及48小时和72小时的基因表达谱之间有很大的相似性。我们还发现,PHx后再生大鼠肝脏中至少有六种不同的基因表达时间模式。

结论

这些结果表明,微阵列分析是监测再生肝脏分子事件的有力方法。

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