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 |
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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. |
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ISSN: | 0363-6143 0002-9513 1522-1563 |
DOI: | 10.1152/ajpcell.1995.269.4.c870 |