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Subcloning, localization, and expression of the rat intestinal sodium-hydrogen exchanger isoform 8.

机译:大鼠肠道钠氢交换异构体8的亚克隆,定位和表达

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Apically expressed intestinal and renal sodium-hydrogen exchangers (NHEs) play a major role in Na(+) absorption. Our previous studies on NHE ontogeny have shown that NHE-2 and NHE-3 are expressed at very low levels in young animals. Furthermore, single and/or double NHE-2 and NHE-3 knockout mice display no obvious abnormalities before weaning. These observations suggest that other transporter(s) may be involved in intestinal Na+ absorption during early life. The present studies were designed to clone the novel rat intestinal NHE-8 cDNA and to decipher the NHE-8 protein localization and gene expression pattern during different developmental stages. The rat NHE-8 cDNA has 2,160 bp and encodes a 575-amino acid protein. An antibody against NHE-8 protein was developed. Immunohistochemistry staining indicated apical localization of NHE-8 protein in rat intestinal epithelial cells. The apical localization of NHE-8 was also confirmed by its presence in brush-border membrane and its absence in basolateral membrane preparations. Northern blotting utilizing a NHE-8-specific probe demonstrated higher NHE-8 mRNA expression in young animals compared with adult animals. Western blot analysis revealed a similar pattern. Tissue distribution with multiple human tissue RNA blot showed that NHE-8 was expressed in multiple tissues including the gastrointestinal tract. In conclusion, we have cloned the full-length NHE-8 cDNA from rat intestine and further showed its apical localization in intestinal epithelial cells. We have also shown that NHE-8 gene expression and protein expression were regulated during ontogeny. Our data suggests that NHE-8 may play an important role in intestinal Na+ absorption during early life.
机译:顶端表达的肠和肾钠氢交换剂(NHEs)在Na(+)吸收中起主要作用。我们先前对NHE个体发育的研究表明NHE-2和NHE-3在幼小动物中的表达水平非常低。此外,单只和/或两只NHE-2和NHE-3基因敲除小鼠在断奶前没有明显的异常。这些观察结果表明,在生命的早期,其他转运蛋白可能参与了肠道对Na +的吸收。本研究旨在克隆新型大鼠肠道NHE-8 cDNA,并在不同发育阶段破译NHE-8蛋白的定位和基因表达模式。大鼠NHE-8 cDNA长2160 bp,编码575个氨基酸。开发了针对NHE-8蛋白的抗体。免疫组织化学染色表明NHE-8蛋白在大鼠肠上皮细胞中顶端定位。 NHE-8的根尖定位还通过其在刷状边界膜中的存在和在基底外侧膜制剂中的不存在来证实。与成年动物相比,利用NHE-8特异性探针进行的Northern印迹显示,幼小动物的NHE-8 mRNA表达更高。蛋白质印迹分析揭示了相似的模式。多种人体组织RNA印迹的组织分布表明NHE-8在包括胃肠道在内的多种组织中表达。总之,我们已经从大鼠肠中克隆了全长NHE-8 cDNA,并进一步显示了其在肠上皮细胞中的顶端定位。我们还表明,NHE-8基因表达和蛋白质表达在个体发育过程中受到调节。我们的数据表明,NHE-8可能在生命早期的肠道Na +吸收中起重要作用。

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