Jaber L, Kan F W
Department of Anatomy and Cell Biology, Faculty of Medicine, Queen's University, Kingston, Ontario, Canada.
Histochem J. 1998 Oct;30(10):711-22. doi: 10.1023/a:1003441904274.
In the present study, we examined by immunohistochemistry the cell-specific distribution of epidermal growth factor (EGF) and platelet-derived growth factor (PDGF) in the mouse uterus during the oestrous cycle and throughout the first 7 days of pregnancy. Paraffin-embedded tissue samples were immunostained using the avidin-biotin peroxidase technique and then examined by light microscopy. Our results showed that immunostaining for EGF was detected in the stroma but not in the luminal or glandular epithelium. A high concentration of EGF was detected in the stroma around the time of embryo implantation at days 3, 4 and 5 of pregnancy. The implanted embryo at day 7 of gestation showed immunostaining for EGF between the ectoderm and endoderm layers. The cell distribution pattern for PDGF was found to be different from that observed with EGF. Luminal and glandular epithelia displayed PDGF immunostaining throughout the first 7 days of pregnancy, with the highest intensity at days 4 and 5 of gestation. In contrast, no immunostaining was observed in the luminal and glandular epithelia at post-oestrus, dioestrus and pro-oestrus stages. However, a weak reaction started to appear at oestrus. The embryo at the blastocyst stage displayed a strong immunoreaction for antibody against PDGF. In addition, the decidual boundary zone surrounding the implanted embryo at days 5, 6 and 7 of gestation also showed an immunostaining for PDGF. The present observations demonstrate clearly the presence of EGF and PDGF in the mouse uterus in high concentrations at the peri-implantation period. Thus, our results, together with what is known about the effect of EGF and PDGF in controlling the growth, differentiation and activation of a variety of cell types, suggest a possible role for these growth factors during the preparation of the endometrium for implantation in controlling the proliferation activity of stromal and/or epithelial cells.
在本研究中,我们通过免疫组织化学方法检测了动情周期以及妊娠前7天小鼠子宫中表皮生长因子(EGF)和血小板衍生生长因子(PDGF)的细胞特异性分布。石蜡包埋的组织样本采用抗生物素蛋白-生物素过氧化物酶技术进行免疫染色,然后通过光学显微镜检查。我们的结果显示,在基质中检测到了EGF免疫染色,而在腔上皮或腺上皮中未检测到。在妊娠第3、4和5天胚胎着床时,基质中检测到高浓度的EGF。妊娠第7天植入的胚胎在外胚层和内胚层之间显示出EGF免疫染色。发现PDGF的细胞分布模式与EGF不同。在妊娠的前7天,腔上皮和腺上皮均显示PDGF免疫染色,在妊娠第4和5天强度最高。相比之下,在发情后期、间情期和发情前期,腔上皮和腺上皮中未观察到免疫染色。然而,在发情期开始出现微弱反应。囊胚期的胚胎对PDGF抗体显示出强烈的免疫反应。此外,在妊娠第5、6和7天,围绕植入胚胎的蜕膜边界区也显示出PDGF免疫染色。目前的观察结果清楚地表明,在植入期前后,小鼠子宫中存在高浓度的EGF和PDGF。因此,我们的结果,连同已知的EGF和PDGF在控制多种细胞类型的生长、分化和激活方面的作用,提示这些生长因子在子宫内膜为植入做准备过程中,在控制基质和/或上皮细胞的增殖活性方面可能发挥作用。