Jones C J, Kimber S J, Illingworth I, Aplin J D
Department of Pathological Sciences, University of Manchester, UK.
J Reprod Fertil. 1996 Mar;106(2):241-50. doi: 10.1530/jrf.0.1060241.
Biotinylated lectins from Sambucus nigra (SNA) and Maackia amurensis (MAA), which bind to alpha 2,6-linked and alpha 2,3-linked sialyl residues, respectively, were used as probes to study glycan terminal modifications associated with decidualization in the uterine stroma of pregnant rats and mice. Binding of lectins from Erythrina cristagalli (ECA), Phaseolus vulgaris (leukoagglutinin, L-PHA), Triticum vulgaris (WGA) and Bandeiraea simplicifolia (BSA-1B4) was also examined. Tissues from rats between day 5 and day 8 of gestation and mice between day 5 and day 7 of gestation were fixed in Bouin's solution and embedded in wax prior to lectin histochemistry. On day 7 in rats and day 6 in mice, there was a marked reduction in the binding of SNA in the subluminal decidua surrounding the implantation site. In rats, MAA binding to enlarged decidual cells around the implantation chamber was increased markedly, but there was no change in mice. In both species there was de novo binding of ECA in the SNA-negative area, suggesting that the loss of alpha 2,6-linked sialyl residues unmasks terminal N-acetyl lactosamine. These findings are consistent with previous evidence of a close structural and functional similarity between the artificially induced deciduoma and true decidua of rats and show identical changes to the glycosylation patterns previously found in differentiating rat deciduoma. In both species, therefore, decidua exhibits regionally specific terminal glycosylation. However, the species-specific expression of alpha 2,3-linked sialyl residues suggests distinct patterns of steroidally modulated sialyl transferase expression.
分别与α2,6-连接和α2,3-连接的唾液酸残基结合的接骨木(SNA)和黑水缬草(MAA)的生物素化凝集素被用作探针,以研究与妊娠大鼠和小鼠子宫基质蜕膜化相关的聚糖末端修饰。还检测了刺桐(ECA)、菜豆(白细胞凝集素,L-PHA)、普通小麦(WGA)和单叶豆(BSA-1B4)凝集素的结合情况。妊娠第5天至第8天的大鼠和妊娠第5天至第7天的小鼠的组织在进行凝集素组织化学之前,用Bouin氏液固定并包埋在石蜡中。在大鼠妊娠第7天和小鼠妊娠第6天,植入部位周围腔下蜕膜中SNA的结合明显减少。在大鼠中,MAA与植入腔周围增大的蜕膜细胞的结合显著增加,但在小鼠中没有变化。在这两个物种中,ECA在SNA阴性区域均有新生结合,表明α2,6-连接的唾液酸残基的缺失暴露了末端N-乙酰乳糖胺。这些发现与先前关于人工诱导的蜕膜瘤与大鼠真蜕膜之间存在密切结构和功能相似性的证据一致,并显示出与先前在分化的大鼠蜕膜瘤中发现的糖基化模式相同的变化。因此,在这两个物种中,蜕膜均表现出区域特异性的末端糖基化。然而,α2,3-连接的唾液酸残基的物种特异性表达表明甾体调节的唾液酸转移酶表达模式不同。