Osmolar changes regulate the paracellular permeability of cultured human cervical epithelium

G. I. Gorodeski, B. J. De Santis, J. Goldfarb, W. H. Utian and U. Hopfer Department of Reproductive Biology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA. Extracellular nucleotides induce a biphasic change in the transepithelial electrical conductance (GT) of human...

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Veröffentlicht in:American Journal of Physiology: Cell Physiology 1995-10, Vol.269 (4), p.C870-C877
Hauptverfasser: Gorodeski, G. I, De Santis, B. J, Goldfarb, J, Utian, W. H, Hopfer, U
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Sprache:eng
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Zusammenfassung:G. I. Gorodeski, B. J. De Santis, J. Goldfarb, W. H. Utian and U. Hopfer Department of Reproductive Biology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA. Extracellular nucleotides induce a biphasic change in the transepithelial electrical conductance (GT) of human cervical cells grown on filters: a rapid increase (phase I) followed by a sustained decrease (phase II). To probe the involvement of the intercellular space, its magnitude was varied by manipulating cell volume through changes in extracellular osmolarity. Under baseline conditions [GT = 115 mS/cm2 (approximately 9 omega.cm2)] and during phase II, hypertonic challenges resulted in an increase in GT (0.98% .mosmol-1.l-1 and 0.73%.mosmol-1.l-1, respectively). However, a hypertonic challenge during phase I decreased GT (-0.16%.mosmol-1.l-1). Hypotonic challenges decreased GT during baseline, phase I, and phase II conditions by -1%.mosmol-1.l-1. Similar trends were observed with regard to pyranine permeability. Reduction of extracellular calcium increased GT, abrogated the phase II effect of extracellular ATP, and reversed the effect of a hypertonic challenge. The additive nature of the permeability changes in response to osmotic challenges and to ATP during phase II suggests that different sites are involved in each response, i.e., the resistance of the intercellular space changes with osmolarity and that of the tight junction during phase II.
ISSN:0363-6143
0002-9513
1522-1563
DOI:10.1152/ajpcell.1995.269.4.c870