SOX2
生物
诱导多能干细胞
重编程
滋养层
干细胞
KLF4公司
胚胎干细胞
细胞生物学
体细胞
体细胞核移植
合胞滋养细胞
转录组
原始条纹
细胞
胚胎
遗传学
胎盘
胚泡
原肠化
胎儿
基因
基因表达
胚胎发生
怀孕
作者
Gaël Castel,Dimitri Meistermann,Betty Bretin,Julie Firmin,Justine Blin,Sophie Loubersac,Alexandre Bruneau,Simon Chevolleau,Stéphanie Kilens,Caroline Chariau,Anne Gaignerie,Quentin Francheteau,Harunobu Kagawa,Éric Charpentier,Léa Flippe,Valentin François-Campion,Sandra Haider,Bianca Dietrich,Martin Knöfler,Takahiro Arima
出处
期刊:Cell Reports
[Cell Press]
日期:2020-11-01
卷期号:33 (8): 108419-108419
被引量:145
标识
DOI:10.1016/j.celrep.2020.108419
摘要
Human trophoblast stem cells (hTSCs) derived from blastocysts and first-trimester cytotrophoblasts offer an unprecedented opportunity to study the placenta. However, access to human embryos and first-trimester placentas is limited, thus preventing the establishment of hTSCs from diverse genetic backgrounds associated with placental disorders. Here, we show that hTSCs can be generated from numerous genetic backgrounds using post-natal cells via two alternative methods: (1) somatic cell reprogramming of adult fibroblasts with OCT4, SOX2, KLF4, MYC (OSKM) and (2) cell fate conversion of naive and extended pluripotent stem cells. The resulting induced/converted hTSCs recapitulated hallmarks of hTSCs including long-term self-renewal, expression of specific transcription factors, transcriptomic signature, and the potential to differentiate into syncytiotrophoblast and extravillous trophoblast cells. We also clarified the developmental stage of hTSCs and show that these cells resemble day 8 cytotrophoblasts. Altogether, hTSC lines of diverse genetic origins open the possibility to model both placental development and diseases in a dish.
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