Michalski Stephanie A, Chadchan Sangappa B, Jungheim Emily S, Kommagani Ramakrishna
Department of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine.
Department of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine;
J Vis Exp. 2018 Sep 1(139):57684. doi: 10.3791/57684.
The differentiation of human endometrial stromal cells (HESC) from fibroblast-like appearance into secretory decidua is a transformation required for embryo implantation into the uterine lining of the maternal womb. Improper decidualization has been established as a root cause for implantation failure and subsequent early embryo miscarriage. Therefore, understanding the molecular mechanisms underlying decidualization is advantageous to improving the rate of successful births. In vivo based studies of artificial decidualization are often limiting due to ethical dilemmas associated with human research, as well as translational complications within animal models. As a result, in vitro assays through primary cell culture are often utilized to explore the modulation of decidualization via hormones. This study provides a detailed protocol for the isolation of HESC and subsequent artificial decidualization via the supplementation of hormones to the culturing medium. Further, this study provides a well-designed method to knockdown any gene of interest by utilizing lipid-based siRNA transfections. This protocol permits the optimization of culture purity as well as product yield, thereby maximizing the ability to utilize this model as a reliable method to understand the molecular mechanisms underlying decidualization, and the subsequent quantification of secreted agents by decidualized endometrial stromal cells.
人子宫内膜基质细胞(HESC)从成纤维细胞样外观分化为分泌性蜕膜是胚胎植入母体子宫内膜所必需的转变。蜕膜化异常已被确认为植入失败及随后早期胚胎流产的根本原因。因此,了解蜕膜化的分子机制有利于提高成功分娩率。基于体内的人工蜕膜化研究往往受到限制,这是由于与人体研究相关的伦理困境以及动物模型中的转化复杂性。因此,通过原代细胞培养进行的体外试验常被用于探索激素对蜕膜化的调节作用。本研究提供了详细的HESC分离方案,以及通过向培养基中添加激素进行后续人工蜕膜化的方案。此外,本研究提供了一种精心设计的方法,通过基于脂质的siRNA转染来敲低任何感兴趣的基因。该方案允许优化培养纯度以及产物产量,从而最大限度地提高将该模型用作理解蜕膜化分子机制以及随后对蜕膜化子宫内膜基质细胞分泌因子进行定量的可靠方法的能力。