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Na,K-ATP酶同工型在MDCK和Caco-2上皮细胞中的表达及活性特征

Characterization of Na,K-ATPase isoform expression and activity in MDCK and Caco-2 epithelial cells.

作者信息

Grindstaff K K, Blanco G, Mercer R W

机构信息

Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Epithelial Cell Biol. 1995;4(1):17-24.

PMID:8563791
Abstract

The asymmetric distribution of the Na,K-ATPase in the plasma membrane of epithelial cells is essential to the establishment of the transepithelial Na+ gradient that supports the vectorial transport of ions and solutes. To investigate the changes that occur during the development of polarity, we have characterized Na,K-ATPase expression and activity in two epithelial cell culture lines, Madin Darby canine kidney (MDCK) and Caco-2 cells. RNA and immunoblot analysis of both cell lines demonstrate that only the alpha 1 and beta 1 isoforms are expressed in nonpolarized and polarized cultures. Interestingly, alpha 1 and beta 1 message increases in MDCK cells with the development of polarity, yet there is little change in the amount of protein for either subunit. In contrast, alpha 1 and beta 1 polypeptide expression increases in Caco-2 cells with the development of polarity, even though the amount of both transcripts decreases. The lack of correlation between the changes that occur at the level of the message and protein suggest that appropriate expression is mediated in part by a combination of transcriptional and translational events. Furthermore, while there was a slight decrease in activity in polarized MDCK cells, there was a 1.9 fold increase in Na,K-ATPase activity in the polarized Caco-2 cells as compared to nonpolarized cells. These results demonstrate that the regulation of Na,K-ATPase alpha 1 and beta 1 isoform expression is mediated by a combination of transcriptional and translational events during the development of polarity in both cell lines.

摘要

上皮细胞质膜中钠钾ATP酶的不对称分布对于建立支持离子和溶质向量运输的跨上皮钠梯度至关重要。为了研究极性发育过程中发生的变化,我们对两种上皮细胞系——麦迪逊-达比犬肾(MDCK)细胞和Caco-2细胞中的钠钾ATP酶表达及活性进行了表征。对这两种细胞系的RNA和免疫印迹分析表明,在非极化和极化培养物中仅表达α1和β1亚型。有趣的是,随着极性的发展,MDCK细胞中的α1和β1信使核糖核酸增加,但两个亚基的蛋白量几乎没有变化。相比之下,随着极性的发展,Caco-2细胞中的α1和β1多肽表达增加,尽管两种转录本的量都减少了。信使核糖核酸和蛋白质水平变化之间缺乏相关性表明,适当的表达部分是由转录和翻译事件共同介导的。此外,虽然极化的MDCK细胞中的活性略有下降,但与非极化细胞相比,极化的Caco-2细胞中的钠钾ATP酶活性增加了1.9倍。这些结果表明,在这两种细胞系极性发育过程中,钠钾ATP酶α1和β1亚型表达的调节是由转录和翻译事件共同介导的。

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