Arici A, Engin O, Attar E, Olive D L
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Clin Endocrinol Metab. 1995 Jun;80(6):1908-15. doi: 10.1210/jcem.80.6.7775640.
Implantation is the process by which the blastocyst becomes intimately connected with the maternal endometrium/decidua. The independently developing preimplantation blastocyst then becomes dependent on the maternal environment for its continued development. Although the factors involved in the regulation of blastocyst implantation are incompletely understood, recent studies strongly suggest a critical role for leukemia inhibitory factor (LIF) in mice. We showed previously that LIF acts on human trophoblasts to shift their differentiation toward the anchoring phenotype by increasing the synthesis of fibronectin. In the present study, we first evaluated the temporal expression of LIF in the human endometrium in order to gain further insights into the role of LIF in human implantation. We established the LIF is expressed in the endometrium in a menstrual cycle-dependent manner. The most abundant LIF messenger ribonucleic acid (mRNA) levels are observed in the mid- and late-luteal phase samples. LIF mRNA was also present in decidual tissues of first trimester of pregnancy, but levels were lower than those found in the midluteal endometrium. We then investigated the regulation of LIF expression in human endometrial cells in culture by cytokines, steroid hormones, and growth factors. We could not show any direct stimulatory evidence of steroid hormones (estradiol and progestins) on LIF mRNA expression or protein production by endometrial cells in culture. On the other hand, we showed that interleukin-1, tumor necrosis factor-alpha, platelet-derived growth factor, epidermal growth factor, and transforming growth factor-beta are potent inducers of LIF expression in endometrial stromal cells in culture in a concentration- and time-dependent manner. Interferon-gamma acted to inhibit LIF expression induced by these cytokines. In contrast, we found high constitutive and relatively less regulated levels of LIF mRNA in the endometrial gland cells. The timing of the expression of LIF in the endometrium suggests a potential role in the implantation. The regulation of the expression of LIF may have an important role in the physiological and pathological processes involving human implantation.
着床是囊胚与母体子宫内膜/蜕膜紧密相连的过程。独立发育的着床前囊胚随后依赖母体环境继续发育。尽管囊胚着床调控所涉及的因素尚未完全明了,但最近的研究强烈表明白血病抑制因子(LIF)在小鼠中起关键作用。我们先前表明,LIF作用于人类滋养层细胞,通过增加纤连蛋白的合成使其分化转向锚定表型。在本研究中,我们首先评估了LIF在人类子宫内膜中的时间表达,以便进一步深入了解LIF在人类着床中的作用。我们确定LIF在子宫内膜中的表达呈月经周期依赖性。在黄体中期和晚期样本中观察到最丰富的LIF信使核糖核酸(mRNA)水平。LIF mRNA也存在于妊娠早期的蜕膜组织中,但水平低于黄体中期子宫内膜中的水平。然后,我们研究了细胞因子、类固醇激素和生长因子对培养中的人类子宫内膜细胞LIF表达的调控。我们未能显示类固醇激素(雌二醇和孕激素)对培养中的子宫内膜细胞LIF mRNA表达或蛋白质产生有任何直接刺激作用。另一方面,我们表明白细胞介素-1、肿瘤坏死因子-α、血小板衍生生长因子、表皮生长因子和转化生长因子-β以浓度和时间依赖性方式强力诱导培养中的子宫内膜基质细胞LIF表达。干扰素-γ起到抑制这些细胞因子诱导的LIF表达的作用。相比之下,我们发现子宫内膜腺细胞中LIF mRNA的组成性水平较高且调控相对较少。LIF在子宫内膜中的表达时间表明其在着床中具有潜在作用。LIF表达的调控可能在涉及人类着床的生理和病理过程中起重要作用。