Tarantino S, Verhage H G, Fazleabas A T
Department of Obstetrics and Gynecology, University of Illinois, Chicago 60612.
Endocrinology. 1992 Apr;130(4):2354-62. doi: 10.1210/endo.130.4.1372242.
The baboon uterus begins to synthesize insulin-like growth factor-binding protein-1 (IGFBP-1) in the deep glands of the late secretory endometrium, and this protein then becomes the major secretory product of the term decidua. We hypothesized that the placenta and/or conceptus may regulate the synthesis and secretion of IGFBP-1 by decidualized stromal cells during pregnancy. To test this hypothesis, tissue was obtained from pregnant baboons on days 18, 25, and 32 postovulation. The uterus was separated into three regions: RI (directly below the implantation site), RII (adjacent to the implantation site), and RIII (opposite the implantation site). Portions of the tissue were fixed in Bouin's solution for immunocytochemistry, and the remainder was subdivided into functionalis, basalis, and myometrium and subjected to organ explant culture. The placenta was fixed or cultured separately. Ligand blot analysis of functionalis medium showed that the major IGFBP had a mol wt (Mr) of 29,000-31,000; however, a doublet of 37,000-43,000 Mr and a band at 24,000 Mr were also present. The functionalis from all regions expressed the majority of the IGFBPs, but basalis from RI tissue also secreted the same array of IGFBPs on days 25 and 32. Ligand blot analysis of placental medium proteins revealed a doublet at Mr 37,000-43,000 on days 25 and 32, but not on day 18. Immunoprecipitation followed by ligand blot analysis of medium proteins using polyclonal antibodies to IGFBP-1 and IGFBP-2 and -3 confirmed that IGFBP-1 and -2 were the predominant products of the endometrium and decidua, while IGFBP-3 was synthesized by the placenta. Immunocytochemistry with a monoclonal antibody to IGFBP-1 demonstrated intense glandular epithelial staining in all regions on days 18, 25, and 32. Stromal staining for IGFBP-1 was first evident on day 25 and was only present in stromal cells in intimate contact with the trophoblastic tissue. By day 32, IGFBP-1 expression was not limited to the endometrial-trophoblastic junction, but extended to the deeper stromal cells and included the perivascular regions. IGFBP-1 staining was most intense in RI, but stromal cells at the luminal surface and those surrounding the spiral arteries also showed some staining in RII and RIII on day 32. These studies suggest that the baboon placenta and/or conceptus regulate IGFBP expression in the uterine endometrium during the initial stages of pregnancy.(ABSTRACT TRUNCATED AT 400 WORDS)
狒狒子宫在分泌期晚期子宫内膜的深部腺体开始合成胰岛素样生长因子结合蛋白-1(IGFBP-1),该蛋白随后成为足月蜕膜的主要分泌产物。我们推测,胎盘和/或孕体可能在妊娠期间调节蜕膜化基质细胞对IGFBP-1的合成和分泌。为验证这一假设,在排卵后第18、25和32天从怀孕的狒狒获取组织。子宫被分为三个区域:RI(植入部位正下方)、RII(与植入部位相邻)和RIII(与植入部位相对)。部分组织固定于Bouin溶液用于免疫细胞化学,其余部分再细分为功能层、基底层和肌层并进行器官外植体培养。胎盘单独固定或培养。对功能层培养基进行配体印迹分析显示,主要的IGFBP分子量(Mr)为29,000 - 31,000;不过,也存在Mr为37,000 - 43,000的双峰以及Mr为24,000的条带。所有区域的功能层均表达大部分IGFBP,但RI组织的基底层在第25天和第32天也分泌相同系列的IGFBP。对胎盘培养基蛋白进行配体印迹分析发现,在第25天和第32天有Mr为37,000 - 43,000的双峰,但在第18天没有。使用针对IGFBP-1、IGFBP-2和-3的多克隆抗体对培养基蛋白进行免疫沉淀后再进行配体印迹分析证实,IGFBP-1和-2是子宫内膜和蜕膜的主要产物,而IGFBP-3由胎盘合成。用针对IGFBP-1的单克隆抗体进行免疫细胞化学显示,在第18、25和32天所有区域的腺上皮均有强烈染色。IGFBP-1的基质染色在第25天首次明显,且仅存在于与滋养层组织紧密接触的基质细胞中。到第32天,IGFBP-1的表达不仅限于子宫内膜 - 滋养层交界处,还扩展到更深层的基质细胞并包括血管周围区域。IGFBP-1染色在RI中最强烈,但在第32天,RII和RIII中腔表面的基质细胞以及螺旋动脉周围的基质细胞也有一些染色。这些研究表明,在妊娠初期,狒狒胎盘和/或孕体调节子宫内膜中IGFBP的表达。(摘要截短至400字)