J Physiol Volume 586, Number 16, 3813-3824, August 15, 2008 DOI: 10.1113/jphysiol.2008.154468
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
Nikolay Shcheynikov1,
Dongki Yang1,
Youxue Wang1,
Weizong Zeng1,
Lawrence P. Karniski2,
Insuk So3,
Susan M. Wall4 and
Shmuel Muallem1
1 Department of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
2
Laboratory of Epithelial Transport, Department of Internal Medicine, Veterans Affairs Medical Center and University of Iowa College of Medicine, Iowa City, IA 52242, USA
3
Department of Physiology and Biophysics, Seoul National University College of Medicine, Seoul 110-799, Korea
4
The Renal Division, Department of Medicine, and Department of Physiology, Emory University School of Medicine, Atlanta 30322, GA, USA
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.
(Received 24 March 2008;
accepted after revision 16 June 2008;
first published online 19 June 2008)
Corresponding author S. Muallem: Department of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Email: shmuel.muallem{at}utsouthwestern.edu
N. Shcheynikov and D. Yang contributed equally to this work and are to be regarded as joint first authors.
Copyright © 2008 The Physiological Society.
