大鼠胆总管结扎致长期胆汁淤积时肝脏基因表达的微阵列分析。

K Kojima, M Hosokawa, K Kobayashi, H Tainaka, K Chiba
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引用次数: 0

摘要

胆汁淤积是主要的肝脏疾病之一,可导致进行性肝纤维化和肝硬化。在这项研究中,通过cDNA微阵列分析,研究了大鼠肝脏对胆总管结扎的转录反应,并鉴定了134个在长期胆汁淤积期间表达改变的基因。对这些基因的多时间点数据进行聚类分析,得到7种不同的模式,其中大部分基因被分为3个聚类。两个基因簇由上调基因组成,包括在胆汁淤积早期观察到的可能与脂质代谢破坏和肝纤维化有关的基因,另一个基因簇由下调基因组成,包括一个被认为参与细胞保护机制防止胆汁酸积聚的基因。因为这些基因的表达模式似乎反映了胆汁淤积的分子特征。在这项研究中鉴定的基因特征可能会进一步阐明长期胆汁淤积症的生理和病理特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microarray analysis of hepatic gene expression during long-term cholestasis induced by common bile duct ligation in rats.

Cholestasis is one of the major liver diseases and results in progressive liver fibrosis and cirrhosis. In this study, the transcriptional response of the liver to common bile duct ligation in rats was examined by cDNA microarray analysis, and 134 genes for which expression was altered during long-term cholestasis were identified. Clustering analysis of these genes for multiple time-point data yielded 7 different patterns in which a large portion of the genes was classified into 3 clusters. Two clusters consisted of up-regulated genes, including genes that may be related to disruption of lipid metabolism and liver fibrosis observed in the early stage of cholestasis, and the other cluster consisted of down-regulated genes, including a gene that has been thought to be involved in the mechanism of cell protection against accumulation of bile acids. Since the expression patterns of these genes appear to reflect molecular features of cholestasis. Characterization of the genes identified in this study may shed further light on the physiological and pathological characteristics of long-term cholestasis.

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