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
[81]  
RAVERA S, 2007, AM J PHYSL CELL 0509
[82]   Organic anion transport is the primary function of the SLC17/type I phosphate transporter family [J].
Reimer, RJ ;
Edwards, RH .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2004, 447 (05) :629-635
[83]   Modulation of phosphate uptake and amphotropic murine leukemia virus entry by posttranslational modifications of PIT-2 [J].
Rodrigues, P ;
Heard, JM .
JOURNAL OF VIROLOGY, 1999, 73 (05) :3789-3799
[84]   Transport-deficient Pit2 phosphate transporters still modify cell surface oligomers structure in response to inorganic phosphate [J].
Salaün, C ;
Maréchal, V ;
Heard, JM .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (01) :39-47
[85]   Pit2 assemblies at the cell surface are modulated by extracellular inorganic phosphate concentration [J].
Salaün, C ;
Gyan, E ;
Rodrigues, P ;
Heard, JM .
JOURNAL OF VIROLOGY, 2002, 76 (09) :4304-4311
[86]   Transmembrane topology of PiT-2, a phosphate transporter-retrovirus receptor [J].
Salaün, C ;
Rodrigues, P ;
Heard, JM .
JOURNAL OF VIROLOGY, 2001, 75 (12) :5584-5592
[87]   Sodium-dependent uptake of inorganic phosphate by the intracellular malaria parasite [J].
Saliba, Kevin J. ;
Martin, Rowena E. ;
Broeer, Angelika ;
Henry, Roselani I. ;
McCarthy, C. Siobhan ;
Downie, Megan J. ;
Allen, Richard J. W. ;
Mullin, Kylie A. ;
McFadden, Geoffrey I. ;
Broeer, Stefan ;
Kirk, Kiaran .
NATURE, 2006, 443 (7111) :582-585
[88]  
SAMARZIJA I, 1982, P EUR DIAL TRANS, V19, P779
[89]   Growth-related renal type IINa/Pi cotransporter [J].
Segawa, H ;
Kaneko, I ;
Takahashi, A ;
Kuwahata, M ;
Ito, M ;
Ohkido, I ;
Tatsumi, S ;
Miyamoto, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (22) :19665-19672
[90]   Phosphate transport via Na+-P-i cotransport and anion exchange in lactating rat mammary tissue [J].
Shillingford, JM ;
Calvert, DT ;
Beechey, RB ;
Shennan, DB .
EXPERIMENTAL PHYSIOLOGY, 1996, 81 (02) :273-284