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短期连续部分肝切除术后再生大鼠肝脏的基因表达差异

Gene expression differences of regenerating rat liver in a short interval successive partial hepatectomy.

作者信息

Xu Cun-Shuan, Zhang An-Shi, Han Hong-Peng, Yuan Jin-Yun, Chang Cui-Fang, Li Wen-Qiang, Yang Ke-Jin, Zhao Li-Feng, Li Yu-Chang, Zhang Hui-Yong, Rahman Salman, Zhang Jing-Bo

机构信息

College of Life Sciences, Henan Normal University, Xinxiang 453007, Henan Province, China.

出版信息

World J Gastroenterol. 2004 Sep 15;10(18):2680-9. doi: 10.3748/wjg.v10.i18.2680.

Abstract

AIM

To identify the genes expressed differentially in the regenerating rat liver in a short interval successive partial hepatectomy (SISPH), and to analyze their expression profiles.

METHODS

Five hundred and fifty-one elements selected from subtractive cDNA libraries were conformed to a cDNA microarray (cDNA chip). An extensive gene expression analysis following 0-36-72-96-144 h SISPH was performed by microarray.

RESULTS

Two hundred and sixteen elements were identified either up- or down-regulated more than 2-fold at one or more time points of SISPH. By cluster analysis and generalization analysis, 8 kinds of ramose gene expression clusters were generated in the SISPH. Of the 216 elements, 111 were up-regulated and 105 down-regulated. Except 99 unreported genes, 117 reported genes were categorized into 22 groups based on their biological functions. Comparison of the gene expression in SISPH with that after partial hepatectomy (PH) disclosed that 56 genes were specially altered in SISPH, and 160 genes were simultaneously up-regulated or down-regulated in SISPH and after PH, but in various amount and at different time points.

CONCLUSION

Genes expressed consistently are far less than that intermittently; the genes strikingly increased are much less than that increased only 2-5 fold; the expression trends of most genes in SISPH and in PH are similar, but the expression of 56 genes is specifically altered in SISPH. Microarray combined with suppressive subtractive hybridization can in a large scale effectively identify the genes related to liver regeneration.

摘要

目的

鉴定在大鼠短期连续部分肝切除术(SISPH)后再生肝脏中差异表达的基因,并分析其表达谱。

方法

从消减cDNA文库中选取的551个元件被整合到一个cDNA微阵列(cDNA芯片)上。通过微阵列对SISPH术后0 - 36 - 72 - 96 - 144小时进行广泛的基因表达分析。

结果

在SISPH的一个或多个时间点,有216个元件被鉴定为上调或下调超过2倍。通过聚类分析和综合分析,在SISPH中产生了8种分支状基因表达簇。在这216个元件中,111个上调,105个下调。除99个未报道的基因外,117个已报道基因根据其生物学功能被分为22组。将SISPH中的基因表达与部分肝切除术(PH)后的基因表达进行比较,发现56个基因在SISPH中发生了特异性改变,160个基因在SISPH和PH后同时上调或下调,但数量和时间点不同。

结论

持续表达的基因远少于间歇表达的基因;显著增加的基因远少于仅增加2 - 5倍的基因;SISPH和PH中大多数基因的表达趋势相似,但56个基因的表达在SISPH中发生了特异性改变。微阵列结合抑制性消减杂交能够大规模有效地鉴定与肝再生相关的基因。

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