Kohl B, Herter P, Hülseweh B, Elger M, Hentschel H, Kinne R K, Werner A
Max-Planck-Institut für Molekulare Physiologie, Dortmund, Germany.
Am J Physiol. 1996 Jun;270(6 Pt 2):F937-44. doi: 10.1152/ajprenal.1996.270.6.F937.
The cloning of a renal Na-Pi contransport in system from winter flounder (P eudopleuronectes americanus) has recently been reported. We used this information to answer the questions 1) what is the distribution of the transport protein along the nephron? and 2) how are renal and intestinal transporters related? The distribution of the flounder NaPi-II protein was tested using two antisera raised against partial sequences (amino acids 1-14 and 388-441) of the transporter. Antibody-specific fluorescence was detected at the basolateral membrane of epithelial cells in the proximal tubular segment PII. Two clones corresponding to the renal Na-Pi cotransporter were isolated from a flounder intestinal cDNA library. Their functional properties were determined using Xenopus laevis oocytes. The apparent affinities for Pi [Michaelis constant (K(m)) = 0.063 mM] and Na (K(m) = 45.3 mM), as well as the pH dependency (increasing transport activity with increasing pH), showed the same characteristics in both intestinal and the renal systems. Sequence analysis revealed that the two intestinal clones were 100% homologous to the renal cDNA, Flounder NaPi-II-specific immunofluorescence was observed predominantly at the apical membrane on intestinal cross sections. We report the cloning and expression of the first intestinal Na-Pi cotransport system. This transporter belongs to the small group of proteins that exhibit the same function in the apical and the basolateral membranes of different cells.
最近有报道称克隆出了美洲拟庸鲽(Pseudopleuronectes americanus)肾系统中的钠-磷共转运体。我们利用这一信息来回答以下问题:1)该转运蛋白在肾单位中的分布情况如何?以及2)肾和肠道转运体之间有何关系?使用针对该转运体部分序列(氨基酸1 - 14和388 - 441)产生的两种抗血清,检测了美洲拟庸鲽钠磷共转运蛋白II(NaPi-II)的分布。在近端肾小管节段PII上皮细胞的基底外侧膜检测到了抗体特异性荧光。从美洲拟庸鲽肠道cDNA文库中分离出了两个与肾钠-磷共转运体对应的克隆。利用非洲爪蟾卵母细胞测定了它们的功能特性。在肠道和肾系统中,对磷酸盐的表观亲和力[米氏常数(K(m))= 0.063 mM]和对钠的表观亲和力(K(m) = 45.3 mM),以及pH依赖性(随着pH升高转运活性增加)均表现出相同的特征。序列分析表明,两个肠道克隆与肾cDNA的同源性为100%。在肠道横切面上,美洲拟庸鲽NaPi-II特异性免疫荧光主要出现在顶端膜上。我们报道了首个肠道钠-磷共转运系统的克隆与表达。该转运体属于在不同细胞的顶端膜和基底外侧膜中发挥相同功能的一小类蛋白质。