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低磷饮食对钠/磷共转运体mRNA和蛋白含量以及对卵母细胞磷转运表达的影响。

Effect of low-phosphate diet on sodium/phosphate cotransport mRNA and protein content and on oocyte expression of phosphate transport.

作者信息

Biber J, Caderas G, Stange G, Werner A, Murer H

机构信息

Department of Physiology, University of Zürich, Switzerland.

出版信息

Pediatr Nephrol. 1993 Dec;7(6):823-6. doi: 10.1007/BF01213368.

Abstract

Recently, we have isolated a complementary DNA most likely related to rabbit kidney cortex brush border membrane sodium/phosphate (Na/Pi) cotransport activity [NaPi-1 (1)]. To further elucidate the cellular mechanisms involved in dietary 'adaptation' of renal Na/Pi cotransport, we have exposed young rabbits for 2 weeks to either a low phosphate (Pi) diet (LPD) or a high Pi diet (HPD). Initial linear uptake of Na/Pi cotransport in isolated brush border membrane vesicles was increased in rabbits on a LPD compared with those on a HPD. Injection of equal amounts of total mRNA isolated from kidney cortex of LPD or HPD rabbits into Xenopus laevis oocytes resulted in a higher stimulation of Na-dependent oocyte Pi uptake in LPD than HPD preparations. No difference in the content of 'specific' mRNA (NaPi-1 cDNA probe, Northern blots) and of the content of the 'specific' brush border membrane protein (NaPi-1 antipeptide antibody, Western blots) between LPD and HPD preparations was observed. We conclude that 'chronic' dietary Pi deprivation leads to a protein synthesis-dependent alteration of Na/Pi cotransport activity which does not involve a change in the total amount of a protein related to the recently cloned NaPi-1 protein.

摘要

最近,我们分离出一种互补DNA,它很可能与兔肾皮质刷状缘膜钠/磷酸盐(Na/Pi)协同转运活性[NaPi-1(1)]有关。为了进一步阐明参与肾脏Na/Pi协同转运饮食“适应性”的细胞机制,我们将幼兔分别置于低磷(Pi)饮食(LPD)或高磷饮食(HPD)环境中2周。与HPD组相比,LPD组家兔分离的刷状缘膜囊泡中Na/Pi协同转运的初始线性摄取增加。将等量从LPD或HPD家兔肾皮质分离的总mRNA注射到非洲爪蟾卵母细胞中,结果显示LPD组比HPD组对卵母细胞Pi摄取的钠依赖性刺激更高。在LPD组和HPD组之间,未观察到“特异性”mRNA含量(NaPi-1 cDNA探针,Northern印迹法)和“特异性”刷状缘膜蛋白含量(NaPi-1抗肽抗体,Western印迹法)的差异。我们得出结论,“长期”饮食性Pi缺乏导致Na/Pi协同转运活性发生蛋白质合成依赖性改变,这并不涉及与最近克隆的NaPi-1蛋白相关的蛋白质总量的变化。

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