Møbjerg Nadja, Werner Andreas, Hansen Sofie M, Novak Ivana
Institute of Molecular Biology, University of Copenhagen, August Krogh Building, Universitetsparken 13, 2100 Copenhagen, Denmark.
Pflugers Arch. 2007 Apr;454(1):101-13. doi: 10.1007/s00424-006-0176-0. Epub 2006 Dec 13.
The aim of this study was to elucidate mechanisms of P(i) handling in toads (Bufo bufo). We introduced toads to experimental solutions of various [P(i)] and high P(i) diets and measured urine and lymph [P(i)]. Both lymph and urine [P(i)] increased with increasing P(i) loads, indicating P(i) absorption across skin and intestine. An initial fragment of a NaPi-II type transporter was amplified from kidney, and the full-length sequence was obtained. The protein showed the molecular hallmarks of NaPi-IIb transporters. When expressed in Xenopus oocytes the clone showed unusual pH dependence, but apparent affinity constants for P(i) and Na(+) were in the range of other NaPi-II transporters. Expression profiling showed that the transporter was present in skin, intestine and kidney. Reverse transcription-polymerase chain reaction assays on dissected renal tubules indicated expression in the collecting duct system. Collecting tubules and ducts were isolated, perfused and microelectrode recordings showed electrogenic P(i) transport in apical and basolateral membranes. Taken together, our results show that P(i) is handled by intestine, kidney and skin. The presently cloned NaPi-IIb is a likely candidate involved in P(i) absorption across these epithelia. In addition, electrophysiological experiments suggest that the collecting duct system plays an important role in P(i) homeostasis.
本研究的目的是阐明蟾蜍(Bufo bufo)中无机磷(P(i))处理的机制。我们将蟾蜍置于不同[P(i)]的实验溶液和高P(i)饮食中,并测量尿液和淋巴液中的[P(i)]。淋巴液和尿液中的[P(i)]均随P(i)负荷的增加而升高,表明P(i)可通过皮肤和肠道吸收。从肾脏中扩增出NaPi-II型转运体的初始片段,并获得了全长序列。该蛋白质显示出NaPi-IIb转运体的分子特征。当在非洲爪蟾卵母细胞中表达时,该克隆显示出异常的pH依赖性,但对P(i)和Na(+)的表观亲和常数在其他NaPi-II转运体的范围内。表达谱分析表明该转运体存在于皮肤、肠道和肾脏中。对分离的肾小管进行逆转录-聚合酶链反应分析表明其在集合管系统中表达。分离并灌注集合小管和集合管,微电极记录显示在顶端膜和基底外侧膜上存在电生性P(i)转运。综上所述,我们的结果表明P(i)可通过肠道、肾脏和皮肤进行处理。目前克隆的NaPi-IIb可能是参与这些上皮细胞吸收P(i)的候选者。此外,电生理实验表明集合管系统在P(i)稳态中起重要作用。