Lapehn Samantha, Nair Sidharth, Firsick Evan J, MacDonald James, Thoreson Ciara, Litch James A, Bush Nicole R, Kadam Leena, Girard Sylvie, Myatt Leslie, Prasad Bhagwat, Sathyanarayana Sheela, Paquette Alison G
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, 98101, USA.
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, 98101, USA.
Placenta. 2025 Jan;159:52-61. doi: 10.1016/j.placenta.2024.11.007. Epub 2024 Nov 26.
Selecting an in vitro culture model of the human placenta is challenging due to representation of different trophoblast cell types with distinct biological roles and limited comparative studies that define key characteristics of these models. The aim of this research was to compare the transcriptomes of common in vitro models of the human placenta compared to bulk human placental tissue.
We performed differential gene expression analysis on publicly available transcriptomic data from 7 in vitro models of the human placenta (HTR-8/SVneo, BeWo, JEG-3, JAR, Primary Trophoblasts, Villous Explants, and Trophoblast Stem Cells) and compared to bulk placental tissue from 2 cohort studies (CANDLE and GAPPS) or individual trophoblast cell types derived from bulk placental tissue.
All in vitro placental models had a substantial number of differentially expressed genes (DEGs, FDR<0.01) compared to the CANDLE and GAPPS placentas (Average DEGs = 10,624), and the individual trophoblast cell types (Average DEGs = 5413), indicating that there are vast differences in gene expression. Hierarchical clustering identified 54 gene clusters with distinct expression profiles across placental models, with 23 clusters enriched for specific KEGG pathways. Placental cell lines were classified by fetal sex based on expression of Y-chromosome genes that identified HTR-8/SVneo cells as female origin, while JEG-3, JAR, and BeWo cells are of male origin.
None of the models were a close approximation of the human bulk placental transcriptome, highlighting the challenges with model selection. To enable appropriate model selection, we adapted our data into a web application: "Comparative Transcriptomic Placental Model Atlas (CTPMA)".
由于不同滋养层细胞类型具有不同生物学作用,且定义这些模型关键特征的比较研究有限,因此选择人胎盘的体外培养模型具有挑战性。本研究的目的是将人胎盘常见体外模型的转录组与整体人胎盘组织进行比较。
我们对来自7种人胎盘体外模型(HTR-8/SVneo、BeWo、JEG-3、JAR、原代滋养层细胞、绒毛外植体和滋养层干细胞)的公开转录组数据进行差异基因表达分析,并与来自2项队列研究(CANDLE和GAPPS)的整体胎盘组织或源自整体胎盘组织的单个滋养层细胞类型进行比较。
与CANDLE和GAPPS胎盘(平均差异基因数 = 10,624)以及单个滋养层细胞类型(平均差异基因数 = 5413)相比,所有体外胎盘模型都有大量差异表达基因(差异基因,FDR<0.01),表明基因表达存在巨大差异。层次聚类识别出54个在胎盘模型中具有不同表达谱的基因簇,其中23个簇富含特定的KEGG通路。胎盘细胞系根据Y染色体基因的表达按胎儿性别分类,该基因将HTR-8/SVneo细胞鉴定为女性来源,而JEG-3、JAR和BeWo细胞为男性来源。
没有一个模型能非常接近人整体胎盘转录组,这凸显了模型选择的挑战。为了实现合适的模型选择,我们将数据改编成一个网络应用程序:“比较转录组胎盘模型图谱(CTPMA)”。