SEARCH

SEARCH BY CITATION

References

  • Accardi A, Kolmakova-Partensky L, Williams C & Miller C (2004). Ionic currents mediated by a prokaryotic homologue of CLC Cl- channels. J Gen Physiol 123, 109119.
  • Bachmann O, Reichelt D, Tuo B, Manns MP & Seidler U (2006). Carbachol increases Na+-HCO3 cotransport activity in murine colonic crypts in a M3-, Ca2+/calmodulin-, and PKC-dependent manner. Am J Physiol Gastrointest Liver Physiol 291, G650G657.
  • Bissig M, Hagenbuch B, Stieger B, Koller T & Meier PJ (1994). Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes. J Biol Chem 269, 30173021.
  • Blouquit-Laye S & Chinet T (2007). Ion and liquid transport across the bronchiolar epithelium. Respir Physiol Neurobiol 159, 278282.
  • Campbell C, Cucci RA, Prasad S, Green GE, Edeal JB, Galer CE, Karniski LP, Sheffield VC & Smith RJ (2001). Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Hum Mutat 17, 403411.
  • Choi I, Aalkjaer C, Boulpaep EL & Boron WF (2000). An electroneutral sodium/bicarbonate cotransporter NBCn1 and associated sodium channel. Nature 405, 571575.
  • Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W & Trembath R (1996). Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4. Nat Genet 12, 421423.
  • Detro-Dassen S, Schänzler M, Lauks H, Martin I, zu Berstenhorst SM, Nothmann D, Torres-Salazar D, Hidalgo P, Schmalzing G & Fahlke C (2007). Conserved dimeric subunit stoichiometry of SLC26 multifunctional anion exchangers. J Biol Chem 283, 41774188.
  • Dorwart MR, Shcheynikov N, Wang Y, Stippec S & Muallem S (2007). SLC26A9 is a Cl channel regulated by the WNK kinases. J Physiol 584, 333345.
  • Dorwart MR, Shcheynikov N, Yang D & Muallem S (2008). The solute carrier 26 family of proteins in epithelial ion transport. Physiology (Bethesda) 23, 104114.
  • Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC & Green ED (1997). Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet 17, 411422.
  • Fairman WA & Amara SG (1999). Functional diversity of excitatory amino acid transporters: ion channel and transport modes. Am J Physiol Renal Physiol 277, F481F486.
  • Forlino A, Piazza R, Tiveron C, Della Torre S, Tatangelo L, Bonafe L, Gualeni B, Romano A, Pecora F, Superti-Furga A, Cetta G & Rossi A (2005). A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype. Hum Mol Genet 14, 859871.
  • Haila S, Hastbacka J, Bohling T, Karjalainen-Lindsberg ML, Kere J & Saarialho-Kere U (2001). SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types. J Histochem Cytochem 49, 973982.
  • Haila S, Saarialho-Kere U, Karjalainen-Lindsberg ML, Lohi H, Airola K, Holmberg C, Hastbacka J, Kere J & Hoglund P (2000). The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells. Histochem Cell Biol 113, 279286.
  • Hastbacka J, de la Chapelle A, Mahtani MM, Clines G, Reeve-Daly MP, Daly M, Hamilton BA, Kusumi K, Trivedi B, Weaver A et al. (1994). The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell 78, 10731087.
  • Hastbacka J, Superti-Furga A, Wilcox WR, Rimoin DL, Cohn DH & Lander ES (1996). Sulfate transport in chondrodysplasia. Ann N Y Acad Sci 785, 131136.
  • Höglund P, Haila S, Socha J, Tomaszewski L, Saarialho-Kere U, Karjalainen-Lindsberg ML, Airola K, Holmberg C, de la Chapelle A & Kere J (1996). Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea. Nat Genet 14, 316319.
  • Höglund P, Sormaala M, Haila S, Socha J, Rajaram U, Scheurlen W, Sinaasappel M, de Jonge H, Holmberg C, Yoshikawa H & Kere J (2001). Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea. Hum Mutat 18, 233242.
  • Jacob P, Rossmann H, Lamprecht G, Kretz A, Neff C, Lin-Wu E, Gregor M, Groneberg DA, Kere J & Seidler U (2002). Down-regulated in adenoma mediates apical Cl/HCO3 exchange in rabbit, rat, and human duodenum. Gastroenterology 122, 709724.
  • Karniski LP, Lotscher M, Fucentese M, Hilfiker H, Biber J & Murer H (1998). Immunolocalization of sat-1 sulfate/oxalate/bicarbonate anion exchanger in the rat kidney. Am J Physiol Renal Physiol 275, F79F87.
  • Kim KH, Shcheynikov N, Wang Y & Muallem S (2005). SLC26A7 is a Cl channel regulated by intracellular pH. J Biol Chem 280, 64636470.
  • Ko SB, Shcheynikov N, Choi JY, Luo X, Ishibashi K, Thomas PJ, Kim JY, Kim KH, Lee MG, Naruse S & Muallem S (2002). A molecular mechanism for aberrant CFTR-dependent HCO3 transport in cystic fibrosis. EMBO J 21, 56625672.
  • Kuo SM & Aronson PS (1988). Oxalate transport via the sulfate/HCO3 exchanger in rabbit renal basolateral membrane vesicles. J Biol Chem 263, 97109717.
  • Lohi H, Kujala M, Makela S, Lehtonen E, Kestila M, Saarialho-Kere U, Markovich D & Kere J (2002). Functional characterization of three novel tissue-specific anion exchangers SLC26A7-A8, and -A9. J Biol Chem 277, 1424614254.
  • Lohi H, Lamprecht G, Markovich D, Heil A, Kujala M, Seidler U & Kere J (2003). Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains. Am J Physiol Cell Physiol 284, C769C779.
  • Loriol C, Dulong S, Avella M, Gabillat N, Boulukos K, Borgese F & Ehrenfeld J (2008). Characterization of SLC26A9, facilitation of Cl transport by bicarbonate. Cell Physiol Biochem 22, 1530.
  • Markovich D & Aronson PS (2007). Specificity and regulation of renal sulfate transporters. Annu Rev Physiol 69, 361375.
  • Melvin JE, Park K, Richardson L, Schultheis PJ & Shull GE (1999). Mouse Down-regulated in adenoma (DRA) is an intestinal Cl/HCO3 exchanger and is up-regulated in colon of mice lacking the NHE3 Na+/H+ exchanger. J Biol Chem 274, 2285522861.
  • Melvin JE, Yule D, Shuttleworth T & Begenisich T (2005). Regulation of fluid and electrolyte secretion in salivary gland acinar cells. Annu Rev Physiol 67, 445469.
  • Miller C (2006). ClC chloride channels viewed through a transporter lens. Nature 440, 484489.
  • Moseley RH, Hoglund P, Wu GD, Silberg DG, Haila S, de la Chapelle A, Holmberg C & Kere J (1999). Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea. Am J Physiol Gastrointest Liver Physiol 276, G185G192.
  • Pritchard JB & Renfro JL (1983). Renal sulfate transport at the basolateral membrane is mediated by anion exchange. Proc Natl Acad Sci U S A 80, 26032607.
  • Quondamatteo F, Krick W, Hagos Y, Kruger MH, Neubauer-Saile K, Herken R, Ramadori G, Burckhardt G & Burckhardt BC (2006). Localization of the sulfate/anion exchanger in the rat liver. Am J Physiol Gastrointest Liver Physiol 290, G1075G1081.
  • Regeer RR, Lee A & Markovich D (2003). Characterization of the human sulfate anion transporter (hsat-1) protein and gene (SAT1; SLC26A1). DNA Cell Biol 22, 107117.
  • Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, Kohn LD & Green ED (2000). Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 141, 839845.
  • Royaux IE, Wall SM, Karniski LP, Everett LA, Suzuki K, Knepper MA & Green ED (2001). Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion. Proc Natl Acad Sci U S A 98, 42214226.
  • Satoh H, Susaki M, Shukunami C, Iyama K, Negoro T & Hiraki Y (1998). Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans. J Biol Chem 273, 1230712315.
  • Schaechinger TJ & Oliver D (2007). Nonmammalian orthologs of prestin (SLC26A5) are electrogenic divalent/chloride anion exchangers. Proc Natl Acad Sci U S A 104, 76937698.
  • Shcheynikov N, Ko SB, Zeng W, Choi JY, Dorwart MR, Thomas PJ & Muallem S (2006a). Regulatory interaction between CFTR and the SLC26 transporters. Novartis Found Symp 273, 177186 (Discussion pp. 186–192 and 261–174).
  • Shcheynikov N, Wang Y, Park M, Ko SB, Dorwart M, Naruse S, Thomas PJ & Muallem S (2006b). Coupling modes and stoichiometry of Cl/HCO3 exchange by slc26a3 and slc26a6. J Gen Physiol 127, 511524.
  • Shcheynikov N, Yang D, Wang Y, Zeng W, Karniski LP, So I, Wall SM & Muallem S (2008). The Slc26a4 transporter functions as an electroneutral Cl/I/HCO3 exchanger: role of Slc26a4 and Slc26a6 in I and HCO3 secretion and in regulation of CFTR in the parotid duct. J Physiol 586, 38133824.
  • Simpson JE, Schweinfest CW, Shull GE, Gawenis LR, Walker NM, Boyle KT, Soleimani M & Clarke LL (2007). PAT-1 (Slc26a6) is the predominant apical membrane Cl/HCO3 exchanger in the upper villous epithelium of the murine duodenum. Am J Physiol Gastrointest Liver Physiol 292, G1079G1088.
  • Sindić A, Chang MH, Mount DB & Romero MF (2007). Renal physiology of SLC26 anion exchangers. Curr Opin Nephrol Hypertens 16, 484490.
  • Soleimani M, Greeley T, Petrovic S, Wang Z, Amlal H, Kopp P & Burnham CE (2001). Pendrin: an apical Cl/OH/HCO3 exchanger in the kidney cortex. Am J Physiol Renal Physiol 280, F356F364.
  • Steward MC, Ishiguro H & Case RM (2005). Mechanisms of bicarbonate secretion in the pancreatic duct. Annu Rev Physiol 67, 377409.
  • Torres GE & Amara SG (2007). Glutamate and monoamine transporters: new visions of form and function. Curr Opin Neurobiol 17, 304312.
  • Wall SM (2005). Recent advances in our understanding of intercalated cells. Curr Opin Nephrol Hypertens 14, 480484.
  • Wall SM, Kim YH, Stanley L, Glapion DM, Everett LA, Green ED & Verlander JW (2004). NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl conservation. Hypertension 44, 982987.
  • Wang Y, Soyombo AA, Shcheynikov N, Zeng W, Dorwart M, Marino CR, Thomas PJ & Muallem S (2006). Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3 secretion: relevance to cystic fibrosis. EMBO J 25, 50495057.
  • Wangemann P, Nakaya K, Wu T, Maganti RJ, Itza EM, Sanneman JD, Harbidge DG, Billings S & Marcus DC (2007). Loss of cochlear HCO3 secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model. Am J Physiol Renal Physiol 292, F1345F1353.
  • Xie Q, Welch R, Mercado A, Romero MF & Mount DB (2002). Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1. Am J Physiol Renal Physiol 283, F826F838.
  • Xu J, Henriksnas J, Barone S, Witte D, Shull GE, Forte JG, Holm L & Soleimani M (2005). SLC26A9 is expressed in gastric surface epithelial cells, mediates Cl/HCO3 exchange, and is inhibited by NH4+. Am J Physiol Cell Physiol 289, C493C505.
  • Zhao H, Star RA & Muallem S (1994). Membrane localization of H+ and HCO3 transporters in the rat pancreatic duct. J Gen Physiol 104, 5785.
  • Zheng J, Shen W, He DZ, Long KB, Madison LD & Dallos P (2000). Prestin is the motor protein of cochlear outer hair cells. Nature 405, 149155.