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Am J Physiol Gastrointest Liver Physiol 295: G234-G251, 2008. First published May 29, 2008; doi:10.1152/ajpgi.00366.2007
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HORMONES AND SIGNALING

A synthetic prostone activates apical chloride channels in A6 epithelial cells

Hui Fang Bao,1,3 Lian Liu,1,3 Julie Self,1,3 Billie Jeanne Duke,1,3 Ryuji Ueno,4 and Douglas C. Eaton1,2,3

Departments of 1Physiology and 2Pediatrics and 3The Center for Cell and Molecular Signaling, Emory University School of Medicine, Atlanta, Georgia; and 4Sucampo Pharmaceuticals, Inc., Bethesda, Maryland

Submitted 10 August 2007 ; accepted in final form 22 May 2008

The bicyclic fatty acid lubiprostone (formerly known as SPI-0211) activates two types of anion channels in A6 cells. Both channel types are rarely, if ever, observed in untreated cells. The first channel type was activated at low concentrations of lubiprostone (<100 nM) in >80% of cell-attached patches and had a unit conductance of ~3–4 pS. The second channel type required higher concentrations (>100 nM) of lubiprostone to activate, was observed in ~30% of patches, and had a unit conductance of 8–9 pS. The properties of the first type of channel were consistent with ClC-2 and the second with CFTR. ClC-2's unit current strongly inwardly rectified that could be best fit by models of the channel with multiple energy barrier and multiple anion binding sites in the conductance pore. The open probability and mean open time of ClC-2 was voltage dependent, decreasing dramatically as the patches were depolarized. The order of anion selectivity for ClC-2 was Cl > Br > NO3 > I > SCN, where SCN is thiocyanate. ClC-2 was a "double-barreled" channel favoring even numbers of levels over odd numbers as if the channel protein had two conductance pathways that opened independently of one another. The channel could be, at least, partially blocked by glibenclamide. The properties of the channel in A6 cells were indistinguishable from ClC-2 channels stably transfected in HEK293 cells. CFTR in the patches had a selectivity of Cl > Br >> NO3 {cong} SCN {cong} I. It outwardly rectified as expected for a single-site anion channel. Because of its properties, ClC-2 is uniquely suitable to promote anion secretion with little anion reabsorption. CFTR, on the other hand, could promote either reabsorption or secretion depending on the anion driving forces.

ClC–2; CFTR; single-channel recording; lubiprostone; SPI-0211



Address for reprint requests and other correspondence: D. C. Eaton, Emory Univ. School of Medicine, Dept. of Physiology, Whitehead Biomedical Research Bldg., 615 Michael St., Atlanta, GA 30322 (e-mail: deaton{at}emory.edu)




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Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
K. D. MacDonald, K. R. McKenzie, M. J. Henderson, C. E. Hawkins, N. Vij, and P. L. Zeitlin
Lubiprostone activates non-CFTR-dependent respiratory epithelial chloride secretion in cystic fibrosis mice
Am J Physiol Lung Cell Mol Physiol, November 1, 2008; 295(5): L933 - L940.
[Abstract] [Full Text] [PDF]




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