TY - JOUR
T1 - The Slc26a4 transporter functions as an electroneutral Cl-/ I-/HCO3- exchanger
T2 - Role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct
AU - Shcheynikov, Nikolay
AU - Yang, Dongki
AU - Wang, Youxue
AU - Zeng, Weizong
AU - Karniski, Lawrence P.
AU - So, Insuk
AU - Wall, Susan M.
AU - Muallem, Shmuel
PY - 2008
Y1 - 2008
N2 - Transcellular Cl- and HCO3- transport is a vital function of secretory epithelia and exit across the luminal membrane is mediated by members of the SLC26 transporters in conjunction with cystic fibrosis transmembrane conductance regulator (CFTR) channel. Typically, secretory epithelia express several SLC26 transporters in the same tissue; however, how their specific function is determined in vivo is not known. In the present work we used the parotid gland duct which expressed Slc26a4 and Slc26a6 and the model systems of Slc26a4-/- and Slc26a6-/- mice to study the role and regulation of these SLC26 transporters. We examined the transport modes of SLC26A4 expressed in Xenopus oocytes and report that SLC26A4 functions as a coupled, electroneutral I-/Cl-, I-/HCO3- and Cl-/HCO3- exchanger with 1: 1 stoichiometry, with I- as the preferred anion. In the duct, Slc26a4 is expressed in the luminal membrane and mainly mediates I- secretion with minimal role in luminal HCO3- transport. By contrast, Slc26a6 mediates luminal Cl-/HCO3- exchange activity with minimal role in I- secretion. Furthermore, silencing of CFTR altered Cl-/HCO3- exchange by Slc26a6, but had no effect on I- secretion by Slc26a4. Accordingly, deletion of Slc26a6, but not deletion of Slc26a4, results in dysregulation of CFTR. These findings provide the first evidence for a selective role of the SLC26 transporters expressed in the same tissue in epithelial anion transport and suggest that transport specificity is achieved by both the properties of the transporters and the composition of the complexes they form.
AB - Transcellular Cl- and HCO3- transport is a vital function of secretory epithelia and exit across the luminal membrane is mediated by members of the SLC26 transporters in conjunction with cystic fibrosis transmembrane conductance regulator (CFTR) channel. Typically, secretory epithelia express several SLC26 transporters in the same tissue; however, how their specific function is determined in vivo is not known. In the present work we used the parotid gland duct which expressed Slc26a4 and Slc26a6 and the model systems of Slc26a4-/- and Slc26a6-/- mice to study the role and regulation of these SLC26 transporters. We examined the transport modes of SLC26A4 expressed in Xenopus oocytes and report that SLC26A4 functions as a coupled, electroneutral I-/Cl-, I-/HCO3- and Cl-/HCO3- exchanger with 1: 1 stoichiometry, with I- as the preferred anion. In the duct, Slc26a4 is expressed in the luminal membrane and mainly mediates I- secretion with minimal role in luminal HCO3- transport. By contrast, Slc26a6 mediates luminal Cl-/HCO3- exchange activity with minimal role in I- secretion. Furthermore, silencing of CFTR altered Cl-/HCO3- exchange by Slc26a6, but had no effect on I- secretion by Slc26a4. Accordingly, deletion of Slc26a6, but not deletion of Slc26a4, results in dysregulation of CFTR. These findings provide the first evidence for a selective role of the SLC26 transporters expressed in the same tissue in epithelial anion transport and suggest that transport specificity is achieved by both the properties of the transporters and the composition of the complexes they form.
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U2 - 10.1113/jphysiol.2008.154468
DO - 10.1113/jphysiol.2008.154468
M3 - Article
C2 - 18565999
AN - SCOPUS:50049122837
SN - 0022-3751
VL - 586
SP - 3813
EP - 3824
JO - Journal of Physiology
JF - Journal of Physiology
IS - 16
ER -