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首页> 外文期刊>American Journal of Physiology >Eel urea transporter is localized to chloride cells and is salinity dependent.
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Eel urea transporter is localized to chloride cells and is salinity dependent.

机译:鳗鱼尿素转运蛋白位于氯化物细胞中,并且与盐分有关。

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摘要

Urea transporters (UTs) in the ureotelic vertebrates have been well-characterized, but little is known about those of the ammonotelic teleost fishes. To clarify the physiological roles of UTs in the ammonotelic teleosts, we determined the structure, tissue and cellular localizations, and regulation of expression of eel UT (eUT) by cDNA cloning, Northern analysis, and immunohistochemistry. A full-length cDNA (approximately 1.9 kb) coding for a UT of 486 amino acid residues was isolated from a seawater eel gill cDNA library. Sequence comparison with those of other species indicated that the eUT is a short isoform with 10 transmembrane spans and has longer NH2- and COOH-terminal cytoplasmic tails compared with the mammalian counterparts. Northern blot analysis demonstrated high expression of eUT mRNA confined in the gill and a substantial increase of its levels when eels were transferred from freshwater to seawater. Immunohistochemistry showed that eUT is localized on the basolateral membranes of the chloride cells, establishing, at the cellular level, the site of urea excretion in the eel, an ammonotelic teleost.
机译:尿素化脊椎动物中的尿素转运蛋白(UTs)具有很好的特征,但对单端硬骨鱼类的尿素转运蛋白知之甚少。为了阐明UTs在单性硬骨鱼中的生理作用,我们通过cDNA克隆,Northern分析和免疫组织化学确定了结构,组织和细胞定位以及鳗鱼UT(eUT)表达的调节。从海水鳗gcDNA文库中分离出编码UT的486个氨基酸残基的全长cDNA(约1.9 kb)。与其他物种的序列比较表明,与哺乳动物的对应物相比,eUT是跨膜跨度为10的短同工型,并且具有更长的NH2-和COOH-末端胞质尾巴。 Northern印迹分析表明,当鳗鱼从淡水转移到海水中时,eUT mRNA在ill中的高表达并且其水平显着增加。免疫组织化学表明,eUT定位于氯化物细胞的基底外侧膜上,在细胞水平上建立了鳗鱼硬骨鱼尿素在鳗鱼中的排泄部位。

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