The functional regeneration of syncytiotrophoblast in cultured explants of term placenta
1 Academic Units of Child Health and 2 Obstetrics and Gynaecology, The University of Manchester, St. Mary's Hospital, Manchester M13 0JH, United Kingdom We have investigated the functional characteristics of term human placental villous explants kept in long-term (7-11 days) culture. Fragment...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2001-04, Vol.280 (4), p.1116-R1122 |
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Sprache: | eng |
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Zusammenfassung: | 1 Academic Units of Child Health and 2 Obstetrics and
Gynaecology, The University of Manchester, St. Mary's Hospital,
Manchester M13 0JH, United Kingdom
We have investigated the functional
characteristics of term human placental villous explants kept in
long-term (7-11 days) culture. Fragments of placental villous
tissue (~5-10 mg wet wt) were cultured in supplemented CMRL-1066
culture medium for up to 11 days. After the first day of culture, the
syncytiotrophoblast appeared vacuolated and eventually degenerated.
However, a new syncytiotrophoblast developed by day 4 , being
indistinguishable from that of a fresh placenta by 11 days. Release of
human chorionic gonadotrophin increased and activity of lactate
dehydrogenase in culture medium decreased with culture time. Transport
variables were measured over the first 7 days of culture. Basal
86 Rb efflux was reduced with time in culture and was
inhibited by Ba 2+ , suggesting the efflux was mediated by
K + channels. At all stages of culture, 86 Rb
efflux was stimulated by ATP, hyposmotic medium, and ANG II. A complex
pattern of efflux changes with culture time and type of stimulator was
observed, suggesting that several compartments of the tissue
contributed to stimulated efflux. This culture system provides
opportunities for studies of chronic regulation of placental function.
explant culture; potassium transport; angiotensin II; adenosine
5'-triphosphate; osmolality |
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ISSN: | 0363-6119 1522-1490 |
DOI: | 10.1152/ajpregu.2001.280.4.r1116 |