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Lectin binding characteristics of mouse placental cells

Published online by Cambridge University Press:  01 April 2000

I. J. STEWART
Affiliation:
Human Morphology, School of Medicine, University of Southampton, Southampton, UK Obstetrics and Gynaecology, School of Medicine, University of Southampton, Southampton, UK
C. R. BEBINGTON
Affiliation:
Human Morphology, School of Medicine, University of Southampton, Southampton, UK
D. D. Y. MUKHTAR
Affiliation:
Human Morphology, School of Medicine, University of Southampton, Southampton, UK Obstetrics and Gynaecology, School of Medicine, University of Southampton, Southampton, UK
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Abstract

The lectin binding characteristics of mouse placental cells were examined. Wax embedded tissue sections of placentae from d 14 pregnant mice were stained with 26 lectins, with a wide range of sugar specificities. Cell cultures prepared from d 14 mouse placentae and cultured for 24 h were stained with 7 of the lectins to determine if they could be used as markers for the different trophoblast cells in culture. In tissue sections all placental cell populations bound lectin but no lectin bound specifically to any single trophoblast population. All the lectins which bound to layer 1 cytotrophoblast lining the maternal blood spaces of the labyrinthine placenta also bound to the fetal endothelium of the labyrinthine placenta. Binding of lectin appeared strongest on the adluminal membrane of these cell populations suggesting a role for the carbohydrate moieties in nutrient transfer. Few lectins bound to junctional zone trophoblast. Overall, the binding of lectin to cultured cells did not correlate exactly with lectin binding to the cell populations in tissue sections. The value of lectins as markers for placental cells in culture was therefore found to be limited. Our findings indicate that carbohydrate expression by at least some placental cells may vary in culture from that expressed by the cells in vivo with obvious concerns for the validity of functional in vitro studies.

Type
Research Article
Copyright
© Anatomical Society of Great Britain and Ireland 2000

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