间质细胞
CXCL2型
CXCL1型
趋化因子
20立方厘米
子宫内膜异位症
白细胞介素8
生物
微阵列分析技术
基因表达
癌症研究
病理
基因
医学
免疫学
趋化因子受体
细胞因子
炎症
遗传学
作者
Ruofei Zhu,Kaei Nasu,Yoko Aoyagi,Tomoko Hirakawa,Katsushi Takebayashi,Hisashi Narahara
标识
DOI:10.1016/j.jri.2020.103100
摘要
Endometriosis is a chronic inflammatory disease which is associated with aberrant chemokine expression. We have established a three-dimensional (3D) floating collagen gel culture of human endometriotic cyst stromal cells (ECSCs) as an in vitro model of early-stage fibrosis formation in endometriosis. We evaluated the gene expression profiles of 3D-cultured ECSCs using a gene expression microarray. We identified and confirmed with reverse transcription-polymerase chain reaction that mRNA levels of CXCL1, CXCL2, CXCL3, CXCL8, and CCL20 in 3D-cultured ECSCs were significantly higher than in 2D-cultured ECSCs. The protein levels of CXCL1, CXCL2, CXCL8, and CCL20 in the supernatant of 3D-cultured ECSCs were significantly higher than in 2D-cultured ECSCs. It has been suggested that the 3D-culture model of ECSCs is more suitable for in vitro endometriosis research than 2D-culture. This microarray data provides a new platform to identify the candidate genes involved in the pathogenesis of endometriosis which could be masked in conventional 2D-culture.
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