Siu Shing-Shun Nelson, Choy Mei-Yee, Leung Tse-Ngong, Lau Tze-Kin
Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.
J Soc Gynecol Investig. 2006 Oct;13(7):491-6. doi: 10.1016/j.jsgi.2006.06.003. Epub 2006 Sep 15.
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.
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.
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.
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.
α-2巨球蛋白(A2M)是一种蛋白酶抑制剂,存在于人类和大鼠的蜕膜组织中。在小鼠中,蜕膜A2M可防止滋养层过度侵袭;然而,其在人类蜕膜组织中的作用尚不清楚。A2M也可能影响人类妊娠中的滋养层侵袭,这将反映在基蜕膜中A2M产量的增加。本研究的目的是测定并比较孕早期人类基蜕膜和壁蜕膜中A2M的产量。
从妊娠9至12周接受手术终止妊娠的患者获取人类蜕膜组织。在实时超声引导下通过刮宫获取基蜕膜和壁蜕膜条。组织样本分别固定于10%福尔马林中或速冻,用于免疫组织化学和逆转录聚合酶链反应(RT-PCR)分析。使用曼-惠特尼U检验比较两个部位之间的蛋白质和mRNA产量。
通过免疫组织化学(n = 9)和RT-PCR(n = 10)分析配对的基蜕膜和壁蜕膜。基蜕膜和壁蜕膜之间A2M mRNA表达无显著差异(P = 0.5)。A2M蛋白的免疫组织化学染色强度在基蜕膜中显著高于壁蜕膜(P = 0.004),但阳性染色细胞的范围无显著差异(P = 0.051)。基蜕膜中强烈的A2M染色主要定位于细胞内储存囊泡,这可能提示A2M在该部位的作用。
我们得出结论,A2M在人类基蜕膜和壁蜕膜中的表达模式与该基因在观察到的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,在这个妊娠窗口期,A2M可能不参与调节人类着床和滋养层侵袭。