Chen Dahu, Xu Xueping, Cheon Yong-Pil, Bagchi Milan K, Bagchi Indrani C
Department of Veterinary Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA.
Biol Reprod. 2004 Aug;71(2):508-14. doi: 10.1095/biolreprod.103.024919. Epub 2004 Mar 24.
In rodents, the steroid hormone estrogen (E) profoundly influences the early events in the uterus leading to embryo implantation. It is thought that E triggers the expression of a unique set of genes in the endometrium that in turn control implantation. To identify these E-induced genes, we employed a delayed implantation model system in which embryo attachment to rat endometrium is dependent upon E administration. Using a gene expression screen method, we isolated a number of cDNAs representing mRNAs whose expression is either turned on or turned off in response to an implantation-inducing dose of E. We identified one of these cDNAs as that encoding secretory leukocyte protease inhibitor (SLPI), an inhibitor of serine proteases. The expression of SLPI mRNA was induced in the uteri of ovariectomized rats in response to E, confirming the hormonal regulation of this molecule. Spatiotemporal analysis revealed a biphasic pattern of expression of SLPI mRNA during early pregnancy. A considerable amount of SLPI mRNA was detected in the uterine epithelium on Day 1 of pregnancy. The level of this mRNA, however, declined sharply on Days 2 and 3 of gestation. Interestingly, on Day 4 of gestation, there was a marked resurgence in SLPI mRNA expression in the uterine epithelium. This second burst of SLPI expression diminished by Day 6 of pregnancy. The transient induction of SLPI mRNA during Days 4 and 5 overlapped with the window of implantation in the rat. Although the precise function of SLPI in the uterus eludes us presently, its known effects as a serine protease inhibitor in other tissues and its hormone-induced expression in the rat uterus immediately preceding implantation lead us to propose that this gene plays an important role in controlling excessive proteolysis and inflammation during a critical phase of early pregnancy.
在啮齿动物中,类固醇激素雌激素(E)对子宫内导致胚胎着床的早期事件有深远影响。据认为,E会触发子宫内膜中一组独特基因的表达,进而控制着床过程。为了鉴定这些由E诱导的基因,我们采用了一种延迟着床模型系统,其中大鼠子宫内膜上的胚胎附着取决于E的给药。使用基因表达筛选方法,我们分离出了一些代表mRNA的cDNA,其表达会因诱导着床剂量的E而开启或关闭。我们鉴定出其中一个cDNA编码分泌型白细胞蛋白酶抑制剂(SLPI),一种丝氨酸蛋白酶抑制剂。去卵巢大鼠子宫中SLPI mRNA的表达会因E而被诱导,证实了该分子的激素调节作用。时空分析揭示了妊娠早期SLPI mRNA表达的双相模式。在妊娠第1天,子宫上皮中检测到大量的SLPI mRNA。然而,在妊娠第2天和第3天,这种mRNA的水平急剧下降。有趣的是,在妊娠第4天,子宫上皮中SLPI mRNA表达显著回升。SLPI表达的第二次激增在妊娠第6天减弱。妊娠第4天和第5天SLPI mRNA的短暂诱导与大鼠的着床窗口期重叠。尽管目前我们尚不清楚SLPI在子宫中的具体功能,但其在其他组织中作为丝氨酸蛋白酶抑制剂的已知作用以及在大鼠子宫中紧邻着床前的激素诱导表达,使我们推测该基因在妊娠早期关键阶段控制过度蛋白水解和炎症方面发挥重要作用。