Bicarbonate transport in cell physiology and disease

被引:137
作者
Cordat, Emmanuelle [1 ]
Casey, Joseph R. [1 ,2 ]
机构
[1] Univ Alberta, Dept Physiol, Membrane Prot Res Grp, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
关键词
bicarbonate transport; Cl; /HCO3; anion exchanger (AE); Na(+)HCO3 co-transporter (NBC); pH regulation; solute carrier (SLC); volume regulation; RENAL TUBULAR-ACIDOSIS; TRANSMEMBRANE CONDUCTANCE REGULATOR; SOUTHEAST-ASIAN OVALOCYTOSIS; DEFECTIVE ANION TRANSPORT; CHLORIDE-LOSING DIARRHEA; DEPENDENT HCO3-TRANSPORT; SOLUBLE ADENYLYL-CYCLASE; HUMAN ERYTHROCYTE BAND-3; POLARIZED KIDNEY-CELLS; AE2; CL-/HCO3-EXCHANGER;
D O I
10.1042/BJ20081634
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The family of mammalian bicarbonate transport proteins are involved in a wide-range of physiological processes. The importance of bicarbonate transport follows from the biochemistry of HCO, itself. Bicarbonate is the waste product of mitochondrial respiration.HCO3; undergoes pH-dependent conversion into CO, and in doing so converts from a membrane impermeant anion into a gas that call diffuse across membranes. The CO2-HCO3 equilibrium forms the most important pH buffering system Of Our bodies. Bicarbonate transport proteins facilitate the movement of membrane-impermeant HCO, across membranes to accelerate disposal of waste CO,, Control Cellular and whole-body pH, and to regulate fluid movement and acid/base secretion. Defects of bicarbonate transport proteins manifest in diseases of most organ systems. Fourteen gene products facilitate mammalian bicarbonate transport, whose physiology and pathophysiology is discussed in the present review.
引用
收藏
页码:423 / 439
页数:17
相关论文
共 229 条
[51]   Hereditary spherocytosis - Defects in proteins that connect the membrane skeleton to the lipid bilayer [J].
Eber, S ;
Lux, SE .
SEMINARS IN HEMATOLOGY, 2004, 41 (02) :118-141
[52]   Evidence that aquaporin 1 is a major pathway for CO2 transport across the human erythrocyte membrane [J].
Endeward, V. ;
Musa-Aziz, R. ;
Cooper, G. J. ;
Chen, L. -M. ;
Pelletier, M. F. ;
Virkki, L. V. ;
Supuran, C. T. ;
King, L. S. ;
Boron, W. F. ;
Gros, G. .
FASEB JOURNAL, 2006, 20 (12) :1974-1981
[53]   RhAG protein of the Rhesus complex is a CO2 channel in the human red cell membrane [J].
Endeward, Volker ;
Cartron, Jean-Pierre ;
Ripoche, Pierre ;
Gros, Gerolf .
FASEB JOURNAL, 2008, 22 (01) :64-73
[54]   From Anrep's Phenomenon to Myocardial Hypertrophy: Role of the Na+/H+ Exchanger [J].
Ennis, Irene L. ;
Cingolani, Horacio E. ;
Garciarena, Carolina D. ;
Camilion de Hurtado, Maria C. ;
Villa-Abrille, Maria C. ;
Aiello, Ernesto A. ;
Perez, Nestor G. .
CURRENT CARDIOLOGY REVIEWS, 2007, 3 (02) :149-164
[55]   Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) [J].
Everett, LA ;
Glaser, B ;
Beck, JC ;
Idol, JR ;
Buchs, A ;
Heyman, M ;
Adawi, F ;
Hazani, E ;
Nassir, E ;
Baxevanis, AD ;
Sheffield, VC ;
Green, ED .
NATURE GENETICS, 1997, 17 (04) :411-422
[56]   Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome [J].
Everett, LA ;
Belyantseva, IA ;
Noben-Trauth, K ;
Cantos, R ;
Chen, A ;
Thakkar, SI ;
Hoogstraten-Miller, SL ;
Kachar, B ;
Wu, DK ;
Green, ED .
HUMAN MOLECULAR GENETICS, 2001, 10 (02) :153-161
[57]   Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear [J].
Everett, LA ;
Morsli, H ;
Wu, DK ;
Green, ED .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) :9727-9732
[58]   Evidence against aquaporin-1-dependent CO2 permeability in lung and kidney [J].
Fang, XH ;
Yang, BX ;
Matthay, MA ;
Verkman, AS .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 542 (01) :63-69
[59]   Granulosa cells regulate intracellular pH of the murine growing oocyte via gap junctions: development of independent homeostasis during oocyte growth [J].
FitzHarris, G ;
Baltz, JM .
DEVELOPMENT, 2006, 133 (04) :591-599
[60]   Regulated expression of pendrin in rat kidney in response to chronic NH4Cl or NaHCO3 loading [J].
Frische, S ;
Kwon, TH ;
Frokiær, J ;
Madsen, KM ;
Nielsen, S .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2003, 284 (03) :F584-F593