Lack of site-specific production of decidual alpha-2 macroglobulin in human pregnancy.

Shing-Shun Nelson Siu, Mei-Yee Choy, Tse-Ngong Leung, Tze-Kin Lau
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引用次数: 7

Abstract

Background: Alpha-2 Macroglobulin (A2M) is a protease inhibitor that is present in both human and rat decidual tissue. In mice, decidual A2M prevents excessive trophoblastic invasion; however, its role in human decidual tissue is unknown. It is possible that A2M may also influence trophoblast invasion in human pregnancy, which would be reflected in increased A2M production in decidua basalis. The aim of the current study was to determine and compare A2M production from first trimester human decidua basalis and decidua parietalis.

Methods: Human decidual tissues were obtained from patients undergoing surgical termination at 9 to 12 gestational weeks. Strips of decidua basalis and decidua parietalis were obtained by uterine curettage under real-time ultrasound guidance. Tissue samples were fixed in 10% formalin or snap-frozen for immunohistochemistry and reverse transcriptase-polymerase chain reaction (RT-PCR) analysis, respectively. Protein and mRNA production between the two sites were compared using the Mann-Whitney U test.

Results: Paired basal and parietal decidua were analyzed by immunohistochemistry (n = 9) and by RT-PCR (n = 10). There was no significant difference in A2M mRNA expression between decidua basalis and decidua parietalis (P = .5). Immunohistochemical staining intensity for A2M protein was significantly higher in basalis than in parietalis (P = .004), but the extent of positively stained cells were not significantly different (P = .051). Strong A2M staining in decidua basalis was mainly localized in the intracellular storage vesicles, which may suggest a role of A2M in this site.

Conclusions: We conclude that the expression pattern of A2M in human decidua basalis and decidua parietalis is not consistent with an important role of this gene during the observed gestational period. Contrary to its role in rodent implantation, A2M is probably not involved in regulating human implantation and trophoblastic invasion during this gestational window frame.

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人类妊娠中缺乏特异性的α -2巨球蛋白的产生。
背景:α -2巨球蛋白(A2M)是一种存在于人和大鼠个体组织中的蛋白酶抑制剂。在小鼠中,蜕膜A2M可防止滋养细胞过度侵袭;然而,其在人体蜕膜组织中的作用尚不清楚。A2M也可能影响人类妊娠期间滋养细胞的侵袭,这可能反映在基底蜕膜中A2M的产生增加。本研究的目的是确定和比较早期妊娠人基底蜕膜和顶叶蜕膜的A2M产量。方法:取妊娠9 ~ 12周手术终止妊娠患者的人蜕膜组织。实时超声引导下刮取子宫基底蜕膜和顶蜕膜条带。组织样本分别用10%福尔马林固定或速冻进行免疫组织化学和逆转录聚合酶链反应(RT-PCR)分析。使用Mann-Whitney U检验比较两个位点之间的蛋白质和mRNA产量。结果:采用免疫组化(n = 9)和RT-PCR (n = 10)分析配对基底和顶叶蜕膜。基底蜕膜与顶蜕膜A2M mRNA表达差异无统计学意义(P = 0.05)。A2M蛋白在基底细胞的免疫组化染色强度显著高于顶叶细胞(P = 0.004),但阳性染色细胞的程度无显著差异(P = 0.051)。基底蜕膜的强A2M染色主要集中在细胞内储泡,提示A2M可能在该部位起作用。结论:我们认为A2M在人基底蜕膜和顶蜕膜中的表达模式与该基因在妊娠期的重要作用不一致。与其在啮齿动物着床中的作用相反,A2M可能不参与调节人类着床和滋养细胞侵袭。
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