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白血病抑制因子及其受体在人类空孕囊妊娠的蜕膜和绒毛膜中的表达未发生改变。

Expression of leukemia inhibitory factor and its receptor is not altered in the decidua and chorionic villi of human anembryonic pregnancy.

作者信息

Chen Hsin-Fu, Chao Kuang-Han, Shew Jin-Yuh, Yang Yu-Shih, Ho Hong-Nerng

机构信息

Department of Obstetrics and Gynecology, College of Medicine and the Hospital, National Taiwan University.

出版信息

Hum Reprod. 2004 Jul;19(7):1647-54. doi: 10.1093/humrep/deh193. Epub 2004 Jun 4.

Abstract

BACKGROUND

Uterine expression of leukemia inhibitory factor (LIF) is absolutely essential for mouse, and critical for human, embryo implantation. However LIF is not required for post-implantation development of mouse embryo. The objective of this study was to examine the role of LIF system in post-implantation stage of human pregnancy.

METHODS

Tissues from 25 patients with anembryonic pregnancy (AP; blighted ovum) and 25 matched patients with normal pregnancy (NP) were collected. LIF and its receptor beta (LIF-Rbeta) expression in the decidua and chorionic villi were analyzed by semi-quantitative reverse transcription and polymerase chain reaction (RT-PCR), real-time quantitative PCR and immunohistochemical study.

RESULTS

LIF mRNA levels were not different either between different tissues (decidua vs chorionic villi) or between different patients (NP vs AP). LIF-Rbeta mRNA levels were significantly higher in chorionic villi than in decidua but were not different between NP and AP. Immunohistochemical staining supported these findings and showed a predominate expression of LIF-Rbeta in the trophoblast cells.

CONCLUSIONS

This study concluded that at early human post-implantation stage, LIF is produced from both decidua and chorionic villi and may exert its major action on trophoblasts. A baseline expression of LIF and LIF-Rbeta is probably needed for early pregnancy, but AP cannot be accounted for by the defective expression of either LIF or LIF-Rbeta in most circumstances.

摘要

背景

白血病抑制因子(LIF)在子宫中的表达对小鼠胚胎着床绝对必要,对人类胚胎着床也至关重要。然而,LIF对小鼠胚胎着床后的发育并非必需。本研究的目的是探讨LIF系统在人类妊娠着床后阶段的作用。

方法

收集25例空孕囊妊娠(AP)患者和25例匹配的正常妊娠(NP)患者的组织。采用半定量逆转录聚合酶链反应(RT-PCR)、实时定量PCR和免疫组织化学研究分析蜕膜和绒毛膜中LIF及其受体β(LIF-Rβ)的表达。

结果

不同组织(蜕膜与绒毛膜)或不同患者(NP与AP)之间LIF mRNA水平无差异。绒毛膜中LIF-Rβ mRNA水平显著高于蜕膜,但NP与AP之间无差异。免疫组织化学染色支持这些发现,并显示LIF-Rβ在滋养层细胞中主要表达。

结论

本研究得出结论,在人类着床后早期,蜕膜和绒毛膜均产生LIF,且可能主要作用于滋养层细胞。妊娠早期可能需要LIF和LIF-Rβ的基线表达,但在大多数情况下,空孕囊妊娠不能用LIF或LIF-Rβ的表达缺陷来解释。

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