Marwood M, Visser K, Salamonsen L A, Dimitriadis E
Prince Henry's Institute of Medical Research, 246 Clayton Road, Clayton, Victoria, Australia.
Endocrinology. 2009 Jun;150(6):2915-23. doi: 10.1210/en.2008-1538. Epub 2009 Feb 12.
Embryo implantation requires the closely harmonized processes of apposition, attachment, and adhesion of the conceptus to the maternal endometrial epithelium. IL-11 and leukemia inhibitory factor (LIF), two IL-6 family cytokines, are produced by the endometrium and are absolutely required for implantation in mice. We examined the effect of IL-11 and LIF on human endometrial epithelial cell adhesion. Both cytokines increased adhesion of primary human endometrial epithelial cells to fibronectin and collagen IV. IL-11 stimulated, whereas LIF had no effect on the adhesion of trophoblast to endometrial epithelial cells. Focused oligogene arrays were used to identify extracellular matrix and adhesion molecules mRNAs regulated by endometrial epithelial cells. We demonstrated by real-time RT-PCR and antibody arrays that both cytokines increased integrin-alpha2 mRNA and protein by endometrial epithelial cells. Signal transducers and activators of transcription (STAT)-3 inhibition reduced IL-11- and LIF-mediated epithelial cell adhesion to fibronectin, suggesting both cytokines regulated adhesion via phosphorylation of STAT3. Addition of either IL-11 neutralizing antibody and IL-11 or LIF and LIF antagonist to endometrial epithelial cells abolished cytokine induced phosphorylated STAT3. LIF but not IL-11 induced adhesion to collagen IV was reduced by an integrin-alpha2beta1 neutralizing antibody. This study demonstrated that IL-11 and LIF regulated endometrial epithelial cell adhesion, suggesting that targeting IL-11 and LIF may be useful in regulating fertility by either enhancing or blocking implantation.
胚胎着床需要胚泡与母体子宫内膜上皮紧密协调地进行定位、附着和黏附过程。白细胞介素11(IL-11)和白血病抑制因子(LIF)这两种IL-6家族细胞因子由子宫内膜产生,是小鼠着床绝对必需的。我们研究了IL-11和LIF对人子宫内膜上皮细胞黏附的影响。这两种细胞因子均增加了原代人子宫内膜上皮细胞与纤连蛋白和IV型胶原的黏附。IL-11刺激滋养层细胞与子宫内膜上皮细胞的黏附,而LIF对此无影响。利用聚焦寡基因阵列鉴定受子宫内膜上皮细胞调控的细胞外基质和黏附分子mRNA。我们通过实时逆转录聚合酶链反应(RT-PCR)和抗体阵列证明,这两种细胞因子均增加了子宫内膜上皮细胞整合素α2 mRNA和蛋白的表达。信号转导及转录激活因子(STAT)-3抑制降低了IL-11和LIF介导的上皮细胞与纤连蛋白的黏附,提示这两种细胞因子均通过STAT3磷酸化调节黏附。向子宫内膜上皮细胞中添加IL-11中和抗体与IL-11或LIF与LIF拮抗剂可消除细胞因子诱导的磷酸化STAT3。整合素α2β1中和抗体可降低LIF而非IL-11诱导的与IV型胶原的黏附。本研究表明,IL-11和LIF调节子宫内膜上皮细胞黏附,提示靶向IL-11和LIF可能有助于通过增强或阻断着床来调节生育能力。