Chen Hsin-Fu, Chao Kuang-Han, Shew Jin-Yuh, Yang Yu-Shih, Ho Hong-Nerng
Department of Obstetrics and Gynecology, College of Medicine and the Hospital, National Taiwan University.
Hum Reprod. 2004 Jul;19(7):1647-54. doi: 10.1093/humrep/deh193. Epub 2004 Jun 4.
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.
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.
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.
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.
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。
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。
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。
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。