Nasu K, Arima K, Kai K, Fujisawa K, Nishida M, Miyakawa I
Department of Obstetrics and Gynecology, Oita Medical University, Hasama-machi, Oita 879-5593, Japan.
Mol Hum Reprod. 2001 May;7(5):453-8. doi: 10.1093/molehr/7.5.453.
It has been demonstrated that human endometrial stromal cells (ESC) produce a variety of chemokines in vivo and in vitro. To evaluate the expression of epithelial neutrophil-activating peptide 78 (ENA-78) in the endometrium, concentrations of ENA-78 in cyclic endometrial tissues were measured using enzyme-linked immunosorbent assay. The expression of ENA-78 was also detected in cyclic endometrium by immunohistochemistry. Endometrial tissues in the secretory phase contained higher amounts of ENA-78 protein than did those in the proliferative phase. Immunofluorescence staining revealed that ENA-78 protein was localized mainly in the stroma of endometrium. In addition, to evaluate the involvement of inflammatory mediators and ovarian steroid hormones in the production of ENA-78 by ESC was evaluated by in-vitro studies. Unstimulated ESC constitutively secreted ENA-78. Progesterone, lipopolysaccharide, tumour necrosis factor-alpha, and interleukin-1beta significantly stimulated the expression of ENA-78 by ESC. It is suggested that the production of ENA-78 by ESC is regulated by progesterone as well as by the inflammatory mediators. The modulation of ENA-78 concentration in the local environment by these mediators may contribute to the normal and pathological processes of human reproduction through regulation of leukocyte trafficking into the endometrium.
已证实,人子宫内膜基质细胞(ESC)在体内和体外均可产生多种趋化因子。为评估子宫内膜中上皮中性粒细胞激活肽78(ENA-78)的表达,采用酶联免疫吸附测定法检测了周期性子宫内膜组织中ENA-78的浓度。还通过免疫组织化学法检测了周期性子宫内膜中ENA-78的表达。分泌期子宫内膜组织中ENA-78蛋白的含量高于增殖期。免疫荧光染色显示,ENA-78蛋白主要定位于子宫内膜的基质中。此外,通过体外研究评估了炎症介质和卵巢甾体激素在ESC产生ENA-78过程中的作用。未受刺激的ESC可组成性分泌ENA-78。孕酮、脂多糖、肿瘤坏死因子-α和白细胞介素-1β可显著刺激ESC表达ENA-78。提示ESC产生ENA-78受孕酮以及炎症介质的调节。这些介质对局部环境中ENA-78浓度的调节可能通过调控白细胞向子宫内膜的迁移,对人类生殖的正常和病理过程产生影响。