Derivation of Mouse Haploid Trophoblast Stem Cells

被引:19
|
作者
Cui, Tongtong [1 ,2 ,3 ]
Jiang, Liyuan [1 ,2 ,4 ]
Li, Tianda [1 ,2 ]
Teng, Fei [1 ,2 ,3 ]
Feng, Guihai [1 ,2 ]
Wang, Xuepeng [1 ,2 ,3 ]
He, Zhengquan [1 ,2 ,3 ]
Guo, Lu [1 ,2 ,3 ]
Xu, Kai [1 ,2 ,3 ]
Mao, Yihuan [1 ,2 ,3 ]
Wang, Leyun [1 ,2 ]
Yuan, Xuewei [1 ,2 ,4 ]
Wang, Liu [1 ,2 ,3 ]
Li, Wei [1 ,2 ,3 ]
Zhou, Qi [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Inst Stem Cell & Regenerat, Beijing 100101, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Northeast Agr Univ, Coll Life Sci, Harbin 150030, Heilongjiang, Peoples R China
来源
CELL REPORTS | 2019年 / 26卷 / 02期
基金
中国国家自然科学基金;
关键词
GENERATION; FATE; CHIMERAS;
D O I
10.1016/j.celrep.2018.12.067
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trophoblast stem (TS) cells are increasingly used as a model system for studying placentation and placental disorders. However, practical limitations of genetic manipulation have posed challenges for genetic analysis using TS cells. Here, we report the generation of mouse parthenogenetic haploid TS cells (haTSCs) and show that supplementation with FGF4 and inhibition of Rho-associated protein kinase (ROCK) enable the maintenance of their haploidy and developmental potential. The resulting haTSCs have 20 chromosomes, exhibit typical expression features of TS cells, possess the multipotency to differentiate into specialized trophoblast cell types, and can chimerize E13.5 and term placentas. We also demonstrate the capability of the haTSCs to undergo genetic manipulation and facilitate genome-wide screening in the trophoblast lineage. We expect that haTSCs will offer a powerful tool for studying functional genomics and placental biology.
引用
收藏
页码:407 / +
页数:13
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