Oshina Kyoko, Kuroda Keiji, Nakabayashi Kazuhiko, Tomikawa Junko, Kitade Mari, Sugiyama Rikikazu, Hata Kenichiro, Itakura Atsuo
Department of Maternal-Fetal Biology, National Center for Child Health and Development, Setagaya, Tokyo, Japan.
Department of Obstetrics and Gynecology, Juntendo University Faculty of Medicine, Bunkyo, Tokyo, Japan.
Front Med (Lausanne). 2023 Jul 20;10:1185284. doi: 10.3389/fmed.2023.1185284. eCollection 2023.
Chronic endometritis (CE) is a persistent inflammatory condition of the endometrium characterized by the infiltration of plasma cells in the endometrial stroma. CD138 immunohistochemistry is considered to improve the CE diagnosis rate.
Using the number of CD138-positive cells equal or greater than five as a diagnostic criterion for CE, we identified 24 CE and 33 non-CE cases among women with infertility. We conducted RNA-sequencing analysis for these 57 cases in total as an attempt to elucidate the molecular pathogenesis of CE and to search for new biomarkers for CE.
By comparing CE and non-CE groups, we identified 20 genes upregulated in the endometria of CE patients, including 12 immunoglobulin-related genes and eight non-immunoglobulin genes as differentially expressed genes. The eight genes were , , , , , , , and . By analyzing samples in the proliferative and secretory phases of the menstrual cycle separately, we also identified four additional non-immunoglobulin genes upregulated in CE endometria: by comparing the samples in the proliferative phase, and , , and by comparing the samples in the secretory phase. Although the genes upregulated in CE may serve as novel diagnostic markers of CE, many of them were upregulated only in a limited number of CE cases showing an extremely high number of CD138-positive cells near or over one hundred. Exceptionally, was upregulated in the majority of CE cases regardless of the number of -positive cells. The upregulation of in the endometria of CE cases may reflect the pathophysiology of a cell-type or cell-types intrinsic to the endometrium rather than the accumulation of plasma cells. Our data, consisting of clinical and transcriptomic information for CE and non-CE cases, helped us identify gene expression signatures associated with CE.
慢性子宫内膜炎(CE)是子宫内膜的一种持续性炎症状态,其特征为子宫内膜间质中浆细胞浸润。CD138免疫组化被认为可提高CE的诊断率。
以CD138阳性细胞数等于或大于5个作为CE的诊断标准,我们在不孕女性中鉴定出24例CE病例和33例非CE病例。我们对这57例病例进行了RNA测序分析,试图阐明CE的分子发病机制并寻找CE的新生物标志物。
通过比较CE组和非CE组,我们在CE患者的子宫内膜中鉴定出20个上调基因,包括12个免疫球蛋白相关基因和8个非免疫球蛋白基因作为差异表达基因。这8个基因分别是 , , , , , , , 。通过分别分析月经周期增殖期和分泌期的样本,我们还在CE子宫内膜中鉴定出另外4个上调的非免疫球蛋白基因:在增殖期样本比较中鉴定出 ,在分泌期样本比较中鉴定出 , , 。虽然CE中上调的基因可能作为CE的新型诊断标志物,但其中许多基因仅在少数CD138阳性细胞数接近或超过100个的CE病例中上调。例外的是,无论 -阳性细胞数多少, 在大多数CE病例中均上调。CE病例子宫内膜中 的上调可能反映了子宫内膜固有细胞类型或细胞类型的病理生理学,而非浆细胞的积累。我们由CE和非CE病例的临床和转录组信息组成的数据,帮助我们鉴定出与CE相关的基因表达特征。