Moretto Zita Matteo, Soncin Francesca, Natale David, Pizzo Donald, Parast Mana
From the Departments of Pathology and.
Reproductive Medicine, University of California San Diego, La Jolla, California 92093.
J Biol Chem. 2015 Dec 11;290(50):30152-62. doi: 10.1074/jbc.M115.659094. Epub 2015 Oct 21.
Appropriate self-renewal and differentiation of trophoblast stem cells (TSCs) are key factors for proper placental development and function and, in turn, for appropriate in utero fetal growth. To identify novel TSC-specific genes, we performed genome-wide expression profiling of TSCs, embryonic stem cells, epiblast stem cells, and mouse embryo fibroblasts, derived from mice of the same genetic background. Our analysis revealed a high expression of Sox21 in TSCs compared with other cell types. Sox21 levels were high in undifferentiated TSCs and were dramatically reduced upon differentiation. In addition, modulation of Sox21 expression in TSCs affected lineage-specific differentiation, based on both marker analysis and functional assessment. Our results implicate Sox21 specifically in the promotion of spongiotrophoblast and giant cell differentiation and establish a new mechanism through which trophoblast sublineages are specified.
滋养层干细胞(TSCs)的适当自我更新和分化是胎盘正常发育和功能的关键因素,进而也是子宫内胎儿正常生长的关键因素。为了鉴定新的TSC特异性基因,我们对来自相同遗传背景小鼠的TSCs、胚胎干细胞、上胚层干细胞和小鼠胚胎成纤维细胞进行了全基因组表达谱分析。我们的分析显示,与其他细胞类型相比,Sox21在TSCs中高表达。Sox21水平在未分化的TSCs中较高,而在分化时显著降低。此外,基于标记分析和功能评估,TSCs中Sox21表达的调节影响了谱系特异性分化。我们的结果表明,Sox21特别参与促进海绵滋养层细胞和巨细胞的分化,并建立了一种确定滋养层亚谱系的新机制。