Adhesion molecules in implantation.

J D Aplin
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引用次数: 245

Abstract

At implantation, trophectoderm attaches to the apical uterine luminal epithelial cell surface. Molecular anatomy studies in humans and mice, and data from experimental models have identified several adhesion molecules that could take part in this process: integrins of the alpha v family, trophinin, CD44, cad-11, the H type I and Lewis y oligosaccharides and heparan sulfate. The endometrial cell surface mucin MUC1 may play a role in both steric inhibition of attachment and selective glycan display. After attachment, interstitial trophoblast invasion occurs requiring a new repertoire of adhesive interactions with maternal extracellular matrix as well as stromal and vascular cell populations. Human anchorage sites contain columns of cytotrophoblasts in which self-attachment gives way progressively to adhesion to extracellular matrix and then interstitial migration. The beta 1 integrins are important during these later stages of implantation and placentation.

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黏附分子植入。
着床时,滋养外胚层附着在子宫腔上皮细胞的顶端表面。对人类和小鼠的分子解剖研究以及实验模型的数据已经确定了几种可能参与这一过程的粘附分子:α v家族的整合素、营养素、CD44、cad-11、H型I和Lewis y低聚糖以及硫酸肝素。子宫内膜细胞表面黏液蛋白MUC1可能在附着的空间抑制和选择性聚糖显示中发挥作用。在附着后,间质滋养细胞侵袭发生,需要与母体细胞外基质以及基质和血管细胞群进行新的粘附相互作用。人的锚定位点包含细胞滋养细胞柱,在这些细胞滋养细胞柱中,自我附着逐渐让位给细胞外基质的粘附,然后是间质迁移。β 1整合素在植入和胎盘的后期阶段是重要的。
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