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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS
1Departments of Physiology and Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana 70112; and 2Department of Physiology, University of Texas Health Science Center, San Antonio, Texas 78229
Submitted 29 September 2003 ; accepted in final form 25 March 2004
Rabbit esophageal epithelia actively transport Na+ in a manner similar to that observed in classic electrically tight Na+-absorbing epithelia, such as frog skin. However, the nature of the apical entry step is poorly understood. To address this issue, we examined the electrophysiological and biochemical nature of this channel. Western blotting experiments with epithelial Na+ channel (ENaC) subunit-specific antibodies revealed the presence of all three ENaC subunits in both native and immortalized esophageal epithelial cells. The amino acid sequence of the rabbit
-ENaC cloned from native rabbit esophageal epithelia was not significantly different from that of other published
-ENaC homologs. To characterize the electrophysiological properties of this native apical channel, we utilized nystatin permeabilization to eliminate the electrical contribution of the basolateral membrane in isolated native epithelia mounted in Ussing-type chambers. We find that the previously described apical Na+ channel is nonselective for monovalent cations (Li+, Na+, and K+). Moreover, this channel was not blocked by millimolar concentrations of amiloride. These findings document the presence of a nonselective cation channel in a native Na+ transporting epithelia, a finding that hereto has been thought to be limited to artificial culture conditions. Moreover, our data are consistent with a potential role of ENaC subunits in the formation of a native nonselective cation channel.
epithelial sodium ion channel; nonselective channel; membrane permeabilization; epithelial sodium ion channel
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