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本文引用的文献

1
Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities.小鼠中Npt2的靶向失活会导致严重的肾磷酸盐流失、高钙尿症和骨骼异常。
Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5372-7. doi: 10.1073/pnas.95.9.5372.
2
Electrophysiological characterization of the flounder type II Na+/Pi cotransporter (NaPi-5) expressed in Xenopus laevis oocytes.在非洲爪蟾卵母细胞中表达的比目鱼II型钠/磷酸盐共转运体(NaPi-5)的电生理特性
J Membr Biol. 1997 Nov 1;160(1):9-25. doi: 10.1007/s002329900291.
3
Regulation of sodium-dependent phosphate transport in osteoclasts.破骨细胞中钠依赖性磷酸盐转运的调节
J Clin Invest. 1997 Aug 1;100(3):538-49. doi: 10.1172/JCI119563.
4
Temporal and spatial expression of an intestinal Na+/PO4 3- cotransporter correlates with epithelial transformation during thyroid hormone-dependent frog metamorphosis.甲状腺激素依赖的青蛙变态过程中,肠道Na+/PO4 3-共转运体的时空表达与上皮细胞转化相关。
Dev Genet. 1997;20(1):53-66. doi: 10.1002/(SICI)1520-6408(1997)20:1<53::AID-DVG7>3.0.CO;2-8.
5
A molecular view of proximal tubular inorganic phosphate (Pi) reabsorption and of its regulation.近端肾小管无机磷酸盐(Pi)重吸收及其调节的分子机制。
Pflugers Arch. 1997 Feb;433(4):379-89. doi: 10.1007/s004240050292.
6
Molecular regulation of renal phosphate transport.肾脏磷酸盐转运的分子调控
J Membr Biol. 1996 Nov;154(1):1-9. doi: 10.1007/s002329900127.
7
Na-Pi cotransport in flounder: same transport system in kidney and intestine.比目鱼中的钠-磷共转运:肾脏和肠道中的转运系统相同。
Am J Physiol. 1996 Jun;270(6 Pt 2):F937-44. doi: 10.1152/ajprenal.1996.270.6.F937.
8
Identification and characterization of a widely expressed phosphate transporter/retrovirus receptor family.一个广泛表达的磷酸盐转运体/逆转录病毒受体家族的鉴定与特性分析
Kidney Int. 1996 Apr;49(4):959-63. doi: 10.1038/ki.1996.135.
9
Transport of phosphate by plasma membranes of the jejunum and kidney of the mouse model of hypophosphatemic vitamin D-resistant rickets.低磷性维生素D抵抗性佝偻病小鼠模型空肠和肾脏质膜对磷酸盐的转运
Proc Soc Exp Biol Med. 1993 Jul;203(3):328-35. doi: 10.3181/00379727-203-43607.
10
Expression cloning of human and rat renal cortex Na/Pi cotransport.人和大鼠肾皮质钠/磷共转运体的表达克隆
Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):5979-83. doi: 10.1073/pnas.90.13.5979.

在哺乳动物小肠中表达的一种小鼠II型钠-磷酸共转运体的特性分析。

Characterization of a murine type II sodium-phosphate cotransporter expressed in mammalian small intestine.

作者信息

Hilfiker H, Hattenhauer O, Traebert M, Forster I, Murer H, Biber J

机构信息

Institut of Physiology, University Zürich, CH-8057 Zurich, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14564-9. doi: 10.1073/pnas.95.24.14564.

DOI:10.1073/pnas.95.24.14564
PMID:9826740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC24413/
Abstract

An isoform of the mammalian renal type II Na/Pi-cotransporter is described. Homology of this isoform to described mammalian and nonmammalian type II cotransporters is between 57 and 75%. Based on major diversities at the C terminus, the new isoform is designed as type IIb Na/Pi-cotransporter. Na/Pi-cotransport mediated by the type IIb cotransporter was studied in oocytes of Xenopus laevis. The results indicate that type IIb Na/Pi-cotransport is electrogenic and in contrast to the renal type II isoform of opposite pH dependence. Expression of type IIb mRNA was detected in various tissues, including small intestine. The type IIb protein was detected as a 108-kDa protein by Western blots using isolated small intestinal brush border membranes and by immunohistochemistry was localized at the luminal membrane of mouse enterocytes. Expression of the type IIb protein in the brush borders of enterocytes and transport characteristics suggest that the described type IIb Na/Pi-cotransporter represents a candidate for small intestinal apical Na/Pi-cotransport.

摘要

本文描述了一种哺乳动物肾II型钠/磷酸共转运体的亚型。该亚型与已描述的哺乳动物和非哺乳动物II型共转运体的同源性在57%至75%之间。基于C末端的主要差异,新亚型被设计为IIb型钠/磷酸共转运体。在非洲爪蟾卵母细胞中研究了由IIb型共转运体介导的钠/磷酸共转运。结果表明,IIb型钠/磷酸共转运是生电性的,且与肾II型亚型的pH依赖性相反。在包括小肠在内的各种组织中检测到了IIb型mRNA的表达。使用分离的小肠刷状缘膜通过蛋白质免疫印迹法检测到IIb型蛋白为108 kDa的蛋白质,并且通过免疫组织化学法将其定位在小鼠肠上皮细胞的腔膜上。IIb型蛋白在肠上皮细胞刷状缘中的表达及其转运特性表明,所描述的IIb型钠/磷酸共转运体是小肠顶端钠/磷酸共转运的一个候选者。