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针对Le(y)寡糖的单克隆抗体可抑制小鼠着床。

Monoclonal antibody directed to Le(y) oligosaccharide inhibits implantation in the mouse.

作者信息

Zhu Z M, Kojima N, Stroud M R, Hakomori S, Fenderson B A

机构信息

Department of Pathology, Anatomy, and Cell Biology, Jefferson Medical College Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Biol Reprod. 1995 Apr;52(4):903-12. doi: 10.1095/biolreprod52.4.903.

Abstract

We investigated the role of carbohydrates in blastocyst attachment to the uterine epithelium. Le(y) (Fuc alpha 1-->2Gal beta 1-->4[Fuc alpha 1-->3] GlcNAc) was localized by indirect immunofluorescence to the surface of the mouse blastocyst and uterine epithelium. Western blot analysis showed that Le(y) is carried on many uterine glycoproteins in both pregnant and nonpregnant females; however, new species were detected on Day 4 postcoitum (p.c.) coincident with the onset of uterine receptivity. The function of Le(y) in implantation was tested by injecting monoclonal antibody (mAb) directly into the uterine lumen on Days 3-5 p.c. The effects of intrauterine injections on implantation were scored by comparing the number of viable embryos to the number of CL on Day 10 p.c. Injection of purified anti-Le(y) IgM into the uterine lumen on the afternoon of Day 4 significantly inhibited implantation. This effect was dose-dependent and was obtained during a narrow time window, from 87 to 93 h p.c. Inhibition of implantation was not observed in contralateral uterine horns injected with saline, nor was it observed in uterine horns injected with other anti-carbohydrate mAbs. We conclude that binding of anti-Le(y) to the blastocyst or luminal epithelium masks a ligand involved in implantation. Although the mechanism of inhibition is unknown, we show that Le(y) can interact with another oligosaccharide (H) that has been described as a possible uterine ligand for blastocyst attachment. We hypothesize that Le(y) and H form carbohydrate-carbohydrate interactions that promote close apposition of cell surface membranes during an early step in implantation.

摘要

我们研究了碳水化合物在囊胚附着于子宫上皮过程中的作用。通过间接免疫荧光法将Le(y)(岩藻糖α1→2半乳糖β1→4[岩藻糖α1→3]N-乙酰葡糖胺)定位到小鼠囊胚和子宫上皮的表面。蛋白质免疫印迹分析表明,在怀孕和未怀孕的雌性小鼠中,许多子宫糖蛋白都携带Le(y);然而,在交配后第4天(p.c.)检测到新的糖蛋白种类,这与子宫接受性的开始相一致。通过在交配后第3 - 5天直接向子宫腔内注射单克隆抗体(mAb)来测试Le(y)在着床中的功能。通过比较怀孕第10天时存活胚胎数量与黄体数量来评估子宫内注射对着床的影响。在第4天下午向子宫腔内注射纯化的抗Le(y) IgM可显著抑制着床。这种作用是剂量依赖性的,并且在一个狭窄的时间窗口内出现,即交配后87至93小时。在注射生理盐水的对侧子宫角未观察到着床抑制,在注射其他抗碳水化合物单克隆抗体的子宫角也未观察到。我们得出结论,抗Le(y)与囊胚或腔上皮的结合掩盖了一种参与着床的配体。尽管抑制机制尚不清楚,但我们表明Le(y)可以与另一种寡糖(H)相互作用,H已被描述为囊胚附着的一种可能的子宫配体。我们推测Le(y)和H形成碳水化合物 - 碳水化合物相互作用,在着床的早期步骤中促进细胞表面膜的紧密贴附。

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