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小鼠胎盘细胞的凝集素结合特性

Lectin binding characteristics of mouse placental cells.

作者信息

Stewart J, Bebington C R, Mukhtar D D

机构信息

Human Morphology, School of Medicine, University of Southampton, UK.

出版信息

J Anat. 2000 Apr;196 ( Pt 3)(Pt 3):371-8. doi: 10.1046/j.1469-7580.2000.19630371.x.

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.

摘要

对小鼠胎盘细胞的凝集素结合特性进行了研究。用26种具有广泛糖特异性的凝集素对妊娠第14天小鼠胎盘的石蜡包埋组织切片进行染色。用其中7种凝集素对从妊娠第14天小鼠胎盘制备并培养24小时的细胞培养物进行染色,以确定它们是否可用作培养中不同滋养层细胞的标志物。在组织切片中,所有胎盘细胞群体均结合凝集素,但没有凝集素特异性结合任何单个滋养层群体。所有与迷路胎盘母体血窦内衬的第1层细胞滋养层结合的凝集素也与迷路胎盘的胎儿内皮结合。凝集素在这些细胞群体的腔面膜上的结合似乎最强,表明碳水化合物部分在营养物质转运中起作用。很少有凝集素与连接区滋养层结合。总体而言,凝集素与培养细胞的结合与凝集素与组织切片中细胞群体的结合并不完全相关。因此,发现凝集素作为培养中胎盘细胞标志物的价值有限。我们的研究结果表明,至少一些胎盘细胞的碳水化合物表达在培养中可能与体内细胞表达不同,这显然关系到体外功能研究的有效性。

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