27 research outputs found
ENaCāMembrane Interactions: Regulation of Channel Activity by Membrane Order
Recently, it was reported that the epithelial Na+ channel (ENaC) is regulated by temperature (Askwith, C.C., C.J. Benson, M.J. Welsh, and P.M. Snyder. 2001. Proc. Natl. Acad. Sci. USA. 98:6459ā6463). As these changes of temperature affect membrane lipid order and lipidāprotein interactions, we tested the hypothesis that ENaC activity can be modulated by membrane lipid interactions. Two approaches were used to modulate membrane anisotropy, a lipid orderādependent parameter. The nonpharmacological approach used temperature changes, while the pharmacological one used chlorpromazine (CPZ), an agent known to decrease membrane order, and Gd+3. Experiments used Xenopus oocytes expressing human ENaC. Methods of impedance analysis were used to determine whether the effects of changing lipid order indirectly altered ENaC conductance via changes of membrane area. These data were further corroborated with quantitative morphology on micrographs from oocytes membranes studied via electron microscopy. We report biphasic effects of cooling (stimulation followed by inhibition) on hENaC conductance. These effects were relatively slow (minutes) and were delayed from the actual bath temperature changes. Peak stimulation occurred at a calculated Tmax of 15.2. At temperatures below Tmax, ENaC conductance was inhibited with cooling. The effects of temperature on gNa were distinct from those observed on ion channels endogenous to Xenopus oocytes, where the membrane conductance decreased monoexponentially with temperature (t = 6.2Ā°C). Similar effects were also observed in oocytes with reduced intra- and extracellular [Na+], thereby ruling out effects of self or feedback inhibition. Addition of CPZ or the mechanosensitive channel blocker, Gd+3, caused inhibition of ENaC. The effects of Gd+3 were also attributed to its ability to partition into the outer membrane leaflet and to decrease anisotropy. None of the effects of temperature, CPZ, or Gd+3 were accompanied by changes of membrane area, indicating the likely absence of effects on channel trafficking. However, CPZ and Gd+3 altered membrane capacitance in an opposite manner to temperature, consistent with effects on the membrane-dielectric properties. The reversible effects of both Gd+3 and CPZ could also be blocked by cooling and trapping these agents in the rigidified membrane, providing further evidence for their mechanism of action. Our findings demonstrate a novel regulatory mechanism of ENaC
Interacting domains in the epithelial sodium channel that mediate proteolytic activation
<p>Epithelial Sodium Channel (ENaC) proteolysis at sites in the extracellular loop of the Ī± and Ī³ subunits leads to marked activation. The mechanism of this effect remains debated, as well as the role of the N- and C-terminal fragments of these subunits created by cleavage. We introduced cysteines at sites bracketing upstream and downstream the cleavage regions in Ī± and Ī³ ENaC to examine the role of these fragments in the activated channel. Using thiol modifying reagents, as well as examining the effects of cleavage by exogenous proteases we constructed a functional model that determines the potential interactions of the termini near the cleavage regions. We report that the N-terminal fragments of both Ī± and Ī³ ENaC interact with the channel complex; with interactions between the N-terminal Ī³ and the C-terminal Ī± fragments being the most critical to channel function and activation by exogenous cleavage by subtilisin. Positive charge modification at a.a.135 in the N-terminal fragment of Ī³ exhibited the largest inhibition of channel function. This region was found to interact with the C-terminal Ī± fragment between a.a. 205 and 221; a tract which was previously identified to be the site of subtilisin's action. These data provide the first evidence for the functional channel rearrangement caused by proteolysis of the Ī± and Ī³ subunit and indicate that the untethered N-terminal fragments of these subunits interact with the channel complex.</p
A long isoform of the epithelial sodium channel alpha subunit forms a highly active channel
<p>A long isoform of the human Epithelial Sodium Channel (ENaC) Ī± subunit has been identified, but little data exist regarding the properties or regulation of channels formed by Ī±<sub>728</sub>. The baseline whole cell conductance of oocytes expressing trimeric Ī±<sub>728</sub>Ī²Ī³ channels was 898.1 Ā± 277.2 and 49.59 Ā± 13.2 ĀµS in low and high sodium solutions, respectively, and was 11 and 2 fold higher than the conductances of Ī±<sub>669</sub>Ī²Ī³ in same solutions. Ī±<sub>728</sub>Ī²Ī³ channels were also 2 to 5 fold less sensitive to activation by the serine proteases subtilisin and trypsin than Ī±<sub>669</sub>Ī²Ī³ in low and high Na<sup>+</sup> conditions. The long isoform exhibited lower levels of full length and cleaved protein at the plasma membrane and a rightward shifted sensitivity to inhibition by increases of [Na<sup>+</sup>]<sub>i</sub>. Both channels displayed similar single channel conductances of 4 pS, and both were activated to a similar extent by reducing temperature, altogether indicating that activation of baseline conductance of Ī±<sub>728</sub>Ī²Ī³ was likely mediated by enhanced channel activity or open probability. Expression of Ī±<sub>728</sub> in native kidneys was validated in human urinary exosomes. These data demonstrate that the long isoform of Ī±ENaC forms the structural basis of a channel with different activity and regulation, which may not be easily distinguishable in native tissue, but may underlie sodium hyperabsorption and salt sensitive differences in humans.</p
Methods for stable recording of short-circuit current in a Na+-transporting epithelium
Epithelial Na+ transport as measured by a variety of techniques, including the short-circuit current technique, has been described to exhibit a ārundownā phenomenon. This phenomenon manifests as time-dependent decrease of current and resistance and precludes the ability to carry out prolonged experiments aimed at examining the regulation of this transport. We developed methods for prolonged stable recordings of epithelial Na+ transport using modifications of the short-circuit current technique and commercial Ussing-type chambers. We utilize the polarized MDCK cell line expressing the epithelial Na+ channel (ENaC) to describe these methods. Briefly, existing commercial chambers were modified to allow continuous flow of Ringer solution and precise control of such flow. Chamber manifolds and associated plumbing were modified to allow precise temperature clamp preventing temperature oscillations. Recording electrodes were modified to eliminate the use of KCl and prevent membrane depolarization from KCl leakage. Solutions utilized standard bicarbonate-based buffers, but all gasses were prehydrated to clamp buffer osmolarity. We demonstrate that these modifications result in measurements of current and resistance that are stable for at least 2 h. We further demonstrate that drifts in osmolarity similar to those obtained before prior to our modifications can lead to a decrease of current and resistance similar to those attributed to rundown