单克隆IIC3抗原在体外初级和次级滋养细胞分化过程中的发育调控

Helen J. Hathaway , Bruce S. Babiarz
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引用次数: 10

摘要

单克隆IIC3抗原已被发现在小鼠原发性和继发性血小板细胞分化过程中受到发育调节。细胞表面抗原的表达仅与二倍体和四倍体滋养细胞类型相关。在分化的滋养层巨细胞中,8C DNA的内复制与IIC3细胞表面表达的缺失和细胞质表达的外观有关。这种发育变化不是暂时调节的,而是依赖于滋养细胞的附着和体外生长。表面抗原既没有脱落到培养基中,也没有被糖基化掩盖,而是被滋养层巨细胞内化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental regulation of the monoclonally defined IIC3 antigen during primary and secondary trophoblast differentiation in vitro

The monoclonally defined IIC3 antigen has been found to be developmentally regulated during primary and secondary throphoblast differentiation in the mouse. Cell surface expression of the antigen was associated only with diploid and tetraploid trophoblast cell types. Endoreduplication to 8C DNA in differentiating trophoblast giant cells was associated with a loss of IIC3 cell surface expression and appearance of cytoplasmic expression. This developmental change was not temporally regulated, but dependent on the attachment and outgrowth of the trophoblast in vitro. The surface antigen was neither shed into the media nor masked by glycosylation, but was apparently internalized by the trophoblast giant cells.

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