Phosphate transporters: a tale of two solute carrier families

被引:193
作者
Virkki, Leila V.
Biber, Juerg
Murer, Heini
Forster, Ian C.
机构
[1] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Ctr Integrat Human Physiol, ZIHP, CH-8057 Zurich, Switzerland
关键词
phosphate; cotransport; electrophysiology; structure-function;
D O I
10.1152/ajprenal.00228.2007
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Phosphate is an essential component of life and must be actively transported into cells against its electrochemical gradient. In vertebrates, two unrelated families of Na+ -dependent Pi transporters carry out this task. Remarkably, the two families transport different P-i species: whereas type II Na+/P-i cotransporters (SCL34) prefer divalent HPO42-, type III Na+/P-i cotransporters (SLC20) transport monovalent H2PO4-. The SCL34 family comprises both electrogenic and electroneutral members that are expressed in various epithelia and other polarized cells. Through regulated activity in apical membranes of the gut and kidney, they maintain body P-i homeostasis, and in salivary and mammary glands, liver, and testes they play a role in modulating the Pi content of luminal fluids. The two SLC20 family members PiT-1 and PiT-2 are electrogenic and ubiquitously expressed and may serve a housekeeping role for cell Pi homeostasis; however, also more specific roles are emerging for these transporters in, for example, bone mineralization. In this review, we focus on recent advances in the characterization of the transport kinetics, structure-function relationships, and physiological implications of having two distinct Na+/Pi cotransporter families.
引用
收藏
页码:F643 / F654
页数:12
相关论文
共 122 条
[1]   Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels [J].
Accardi, A ;
Miller, C .
NATURE, 2004, 427 (6977) :803-807
[2]   Renouncing electroneutrality is not free of charge:: Switching on electrogenicity in a Na+-coupled phosphate cotransporter [J].
Bacconi, A ;
Virkki, LV ;
Biber, J ;
Murer, H ;
Forster, IC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (35) :12606-12611
[3]  
BACCONI A, IN PRESS J MEMBR BIO
[4]   Cloning and characterization of a type IIINa-dependent phosphate cotransporter from mouse intestine [J].
Bai, L ;
Collins, JF ;
Ghishan, FK .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 279 (04) :C1135-C1143
[5]   Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities [J].
Beck, L ;
Karaplis, AC ;
Amizuka, N ;
Hewson, AS ;
Ozawa, H ;
Tenenhouse, HS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5372-5377
[6]   Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter [J].
Bellocchio, EE ;
Reimer, RJ ;
Fremeau, RT ;
Edwards, RH .
SCIENCE, 2000, 289 (5481) :957-960
[7]   SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis [J].
Bergwitz, C ;
Roslin, NM ;
Tieder, M ;
Loredo-Osti, JC ;
Bastepe, M ;
Abu-Zahra, H ;
Frappier, D ;
Burkett, K ;
Carpenter, O ;
Anderson, D ;
Garabédian, M ;
Sermet, I ;
Fujiwara, TM ;
Morgan, K ;
Tenenhouse, HS ;
Jüppner, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 78 (02) :179-192
[8]   Evolutionary and experimental analyses of inorganic phosphate transporter PiT family reveals two related signature sequences harboring highly conserved aspartic acids critical for sodium-dependent phosphate transport function of human PiT2 [J].
Bottger, P ;
Pedersen, L .
FEBS JOURNAL, 2005, 272 (12) :3060-3074
[9]   The central half of Pit2 is not required for its function as a retroviral receptor [J].
Bottger, P ;
Pedersen, L .
JOURNAL OF VIROLOGY, 2004, 78 (17) :9564-9567
[10]   Two highly conserved glutamate residues critical for type III sodium-dependent phosphate transport revealed by uncoupling transport function from retroviral receptor function [J].
Bottger, P ;
Pedersen, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) :42741-42747