Feng Qian, Hu Zhuo-Ying, Liu Xue-Qing, Zhang Xue, Lan Xi, Geng Yan-Qing, Chen Xue-Mei, He Jun-Lin, Wang Ying-Xiong, Ding Yu-Bin
Laboratory of Reproductive Biology, School of Public Health and Management, Chongqing Medical University, Box 197, No. 1 Yixueyuan Rd, Chongqing 400016, China.
Department of Obstetrics and Gynaecology, The First Affiliated Hospital, Chongqing Medical University, Building 5 Room 507, No. 1 Youyi Rd, Chongqing 400016, China.
Reprod Biomed Online. 2017 Feb;34(2):191-202. doi: 10.1016/j.rbmo.2016.11.009. Epub 2016 Nov 23.
The molecular mechanisms underlying endometrial stromal cell proliferation and differentiation (decidualization) are still not fully understood. This study revealed that increased Slp-2 expression is a significant factor modulating endometrial stromal cell proliferation and decidualization in both mice and humans. Our results showed a significant difference in the mRNA and protein levels between the implantation site and inter-implantation site on day 5 and day 6 of pregnancy in mice (all P < 0.05). Strong Slp-2 immunostaining was mainly localized within the decidual zone of mice through the post-implantation period. Mice with artificially induced deciduoma showed significantly higher expression of Slp-2 compared with uninduced controls (P < 0.005). Human stromal cells in the middle and late-secretory phases demonstrated significantly (all P < 0.05) upregulated SLP-2, compared with cells in the proliferative phase and early secretory phases. Further analyses of the SLP-2 gene knocked down revealed a significant (P < 0.005) repression of both the decidualization marker gene's expression (decidual/trophoblast prolactin-related protein in mice, insulin-like growth factor binding protein and prolactin in human) and the cell proliferation in in vitro-induced decidualized primary endometrial stromal cells in mice and humans.
子宫内膜基质细胞增殖和分化(蜕膜化)的分子机制仍未完全明确。本研究表明,Slp-2表达增加是调节小鼠和人类子宫内膜基质细胞增殖及蜕膜化的重要因素。我们的结果显示,在小鼠妊娠第5天和第6天,着床部位与非着床部位之间的mRNA和蛋白质水平存在显著差异(所有P<0.05)。在植入后的整个时期,强Slp-2免疫染色主要定位于小鼠的蜕膜区。人工诱导产生蜕膜瘤的小鼠与未诱导的对照组相比,Slp-2表达显著更高(P<0.005)。与增殖期和分泌期早期的细胞相比,分泌期中后期的人基质细胞SLP-2表达显著上调(所有P<0.05)。对敲低SLP-2基因的进一步分析显示,在体外诱导的小鼠和人类原代子宫内膜基质蜕膜化细胞中,蜕膜化标记基因(小鼠中的蜕膜/滋养层催乳素相关蛋白、人类中的胰岛素样生长因子结合蛋白和催乳素)的表达及细胞增殖均受到显著抑制(P<0.005)。