Highet Amanda R, Buckberry Sam, Mayne Benjamin T, Khoda Sultana M, Bianco-Miotto Tina, Roberts Claire T
School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Gene Expr Patterns. 2016 Jul;21(2):103-10. doi: 10.1016/j.gep.2016.05.001. Epub 2016 May 21.
Extravillous cytotrophoblasts isolated from first trimester placenta, and immortalised cell lines derived from them, have the intrinsic ability to form endothelial-like tubes when cultured on Matrigel™ extracellular matrix. This in vitro tube formation may model placental angiogenesis and/or endovascular differentiation by trophoblasts. To interpret the relevance of this phenomenon to placental development, we used a gene expression microarray approach to identify which genes and pathways are associated with the tube-forming phenotype of HTR8/SVneo first trimester trophoblasts (HTR8-M), compared with HTR8/SVneo not forming tubes on plastic culture surface (HTR8-P). Furthermore, we used weighted gene co-expression network analysis (WGCNA) of microarray data to identify modules of co-expressed genes underlying the biological processes. There were 481 genes differentially expressed between HTR8-M and HTR8-P and these were significantly enriched for blood vessel development and related gene ontologies. WGCNA clustered the genes into 9 co-expression modules. One module was significantly associated with HTR8-M (p = 1.15E-05) and contained genes involved in actin cytoskeleton organization, cell migration and blood vessel development, consistent with tube formation on Matrigel. Another module was significantly associated with HTR8-P (p = 1.94E-05) and was enriched for genes involved in mitosis, consistent with proliferation by cells on plastic which do not differentiate. Up-regulation of angiogenesis and vascular development pathways in endovascular trophoblasts in vivo could underpin spiral artery remodelling processes, which are defective in preeclamptic pregnancies.
从孕早期胎盘分离的绒毛外细胞滋养层细胞及其衍生的永生化细胞系,在Matrigel™细胞外基质上培养时具有形成内皮样管的内在能力。这种体外管形成可能模拟胎盘血管生成和/或滋养层细胞的血管内分化。为了解释这一现象与胎盘发育的相关性,我们采用基因表达微阵列方法,以确定与HTR8/SVneo孕早期滋养层细胞(HTR8-M)的管形成表型相关的基因和通路,与在塑料培养表面不形成管的HTR8/SVneo(HTR8-P)进行比较。此外,我们对微阵列数据进行加权基因共表达网络分析(WGCNA),以识别生物过程潜在的共表达基因模块。HTR8-M和HTR8-P之间有481个基因差异表达,这些基因在血管发育和相关基因本体中显著富集。WGCNA将这些基因聚类为9个共表达模块。一个模块与HTR8-M显著相关(p = 1.15E-05),包含参与肌动蛋白细胞骨架组织、细胞迁移和血管发育的基因,这与在Matrigel上形成管一致。另一个模块与HTR8-P显著相关(p = 1.94E-05),并富集了参与有丝分裂的基因,这与在塑料上不分化的细胞增殖一致。体内血管内滋养层细胞中血管生成和血管发育通路的上调可能是螺旋动脉重塑过程的基础,而这一过程在子痫前期妊娠中存在缺陷。