Absorptive apical amiloride-sensitive Na+ conductance in human endometrial epithelium

Human endometrial epithelial cells cultured on porous tissue culture supports formed tight, polarized epithelial monolayers with features characteristic of tight epithelia. Endometrial epithelial layers generated significant transepithelial electrical resistance (750 Ω cm 2 ) and potential differen...

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Published inThe Journal of physiology Vol. 513; no. 2; pp. 443 - 452
Main Authors Matthews, C. Jane, McEwan, Gordon T. A., Redfern, Christopher P. F., Thomas, Eric J., Hirst, Barry H.
Format Journal Article
LanguageEnglish
Published Oxford, UK The Physiological Society 01.12.1998
Blackwell Science Ltd
Blackwell Science Inc
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Summary:Human endometrial epithelial cells cultured on porous tissue culture supports formed tight, polarized epithelial monolayers with features characteristic of tight epithelia. Endometrial epithelial layers generated significant transepithelial electrical resistance (750 Ω cm 2 ) and potential difference (15.3 mV), with an inward short-circuit current ( I sc ; 20.5 μA cm −2 ). The I sc was linearly proportional to the external Na + concentration and was abolished in the absence of Na + . The I sc was sensitive to apical amiloride. Net 22 Na + flux was in the absorptive apical to basolateral direction and fully accounted for the inward I sc . In addition, apical to basolateral and net 22 Na + transport were reduced in the presence of amiloride. The I sc was also sensitive to addition of ouabain and Ba 2+ to the basal solution, consistent with a role for basolateral Na + −K + -ATPase and K + channels in generation of the current. These data demonstrate that human endometrial epithelial cells in primary culture produce tight, functional monolayers on permeable supports. We provide the first evidence that human endometrial epithelial cells have an inward I sc accounted for by an amiloride-sensitive Na + conductance. The Na + -absorptive function of the endometrium may provide an appropriate environment for sperm function and embryo growth.
Bibliography:Authors’ present addresses
E. J. Thomas: Department of Obstetrics and Gynaecology, University of Southampton, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK.
G. T. A. McEwan: Department of Biomedical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB2 2ZD, UK.
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Authors’ present addresses G. T. A. McEwan: Department of Biomedical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen AB2 2ZD, UK.
ISSN:0022-3751
1469-7793
DOI:10.1111/j.1469-7793.1998.443bb.x