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通过微阵列分析评估从正常小鼠分离的小胆管细胞和大胆管细胞中的差异基因表达。

Evaluation of differential gene expression by microarray analysis in small and large cholangiocytes isolated from normal mice.

作者信息

Ueno Yoshiyuki, Alpini Gianfranco, Yahagi Kaichiro, Kanno Noriatsu, Moritoki Yuki, Fukushima Koji, Glaser Shannon, LeSage Gene, Shimosegawa Tooru

机构信息

Division of Gastroenterology, Tohoku University School of Medicine, Seiryo, Aobaku, Sendai, Japan.

出版信息

Liver Int. 2003 Dec;23(6):449-59. doi: 10.1111/j.1478-3231.2003.00876.x.

Abstract

AIMS

We have shown that large and small cholangiocytes, which reside primarily in large and small intrahepatic bile ducts, respectively, have different functions and responses to injuries. However, there are no systematic studies of the molecular differences between small and large cholangiocytes, which would explain cholangiocyte heterogeneity. To evaluate the differential gene expression between small and large cholangiocytes, microarray analysis was performed.

METHODS

Primary cultures of small and large cholangiocytes were isolated from normal mice (BALB/c), and immortalized by the introduction of the SV40 large T antigen gene. After cloning, small and large cholangiocyte cell lines were established. Their characteristic features were confirmed by electron microscopy (EM) and measurement of transepithelial electrical resistance (TER), and secretin-stimulated cAMP levels. Isolated total RNAs were hybridized with microarrays (Atlas Glass Array Mouse 1.0 and 3.8), which detects 4850 cDNA expressions. After hybridization, the fluorescent signals were scanned by a GenePix fluorescent scanner and analyzed using ArrayGauge software.

RESULTS

EM, TER and secretin-stimulated cAMP synthesis are consistent with the concept that small and large immortalized cholangiocytes originate from small and large ducts, respectively. When a cut-off value at the expression signal difference of 3.0 times was employed, 230 cDNAs among 4850 cDNAs (4.74%) were differentially expressed between small and large cholangiocytes. Of these 230 cDNAs, aquaporin 8, IL-2 receptor beta chain and caspase 9 were more strongly expressed by large cholangiocytes.

CONCLUSIONS

Microarray successfully displayed characteristic differential cDNA expression between small and large cholangiocytes. This technique provides molecular information, which further supports our hypothesis that small and large bile ducts have different functions.

摘要

目的

我们已经表明,主要分别存在于肝内大、小胆管中的大、小胆管细胞具有不同的功能和对损伤的反应。然而,目前尚无关于大、小胆管细胞分子差异的系统性研究,而这些差异可以解释胆管细胞的异质性。为了评估大、小胆管细胞之间的基因表达差异,我们进行了微阵列分析。

方法

从小鼠(BALB/c)中分离出大、小胆管细胞的原代培养物,并通过导入SV40大T抗原基因使其永生化。克隆后,建立了大、小胆管细胞系。通过电子显微镜(EM)、跨上皮电阻(TER)测量以及促胰液素刺激的cAMP水平测定来确认它们的特征。分离的总RNA与可检测4850个cDNA表达的微阵列(Atlas Glass Array Mouse 1.0和3.8)杂交。杂交后,用GenePix荧光扫描仪扫描荧光信号,并使用ArrayGauge软件进行分析。

结果

EM、TER以及促胰液素刺激的cAMP合成与以下概念一致,即永生化的大、小胆管细胞分别起源于大、小胆管。当采用表达信号差异为3.0倍的截断值时,4850个cDNA中有230个(4.74%)在大、小胆管细胞之间差异表达。在这230个cDNA中,水通道蛋白8、白细胞介素2受体β链和半胱天冬酶9在大胆管细胞中表达更强。

结论

微阵列成功展示了大、小胆管细胞之间特征性的差异cDNA表达。这项技术提供了分子信息,进一步支持了我们关于大、小胆管具有不同功能的假设。

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