Generation of Isthmic Organizer-Like Cells from Human Embryonic Stem Cells

被引:3
|
作者
Lee, Junwon [1 ,2 ,3 ]
Choi, Sang-Hwi [1 ,3 ]
Lee, Dongjin R. [1 ,3 ]
Kim, Dae-Sung [4 ]
Kim, Dong-Wook [1 ,3 ]
机构
[1] Yonsei Univ, Coll Med, Dept Physiol, Seoul 03722, South Korea
[2] Yonsei Univ, Coll Med, Dept Ophthalmol, Seoul 03722, South Korea
[3] Yonsei Univ, Coll Med, Brain Korea PLUS Project Med Sci 21, Seoul 03722, South Korea
[4] Korea Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Brain Korea PLUS Project Biotechnol 21, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
FGF; human pluripotent stem cells; isthmic organizer; neural differentiation; Wnt; NERVOUS-SYSTEM; ANTERIOR HINDBRAIN; BRAIN-DEVELOPMENT; OTX2; EXPRESSION; MIDBRAIN; WNT; FGF8; FOREBRAIN; NEURONS; MODEL;
D O I
10.14348/molcells.2018.2210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The objective of this study was to induce the production of isthmic organizer (IsO)-like cells capable of secreting fibroblast growth factor (FGF) 8 and WNT1 from human embryonic stem cells (ESCs). The precise modulation of canonical Wnt signaling was achieved in the presence of the small molecule CHIR99021 (0.6 mu M) during the neural induction of human ESCs, resulting in the differentiation of these cells into IsO-like cells having a midbrain-hindbrain border (MHB) fate in a manner that recapitulated their developmental course in vivo. Resultant cells showed upregulated expression levels of FGF8 and WNT1. The addition of exogenous FGF8 further increased WNT1 expression by 2.6 fold. Gene ontology following microarray analysis confirmed that IsO-like cells enriched the expression of MHB-related genes by 40 fold compared to control cells. Lysates and conditioned media of IsO-like cells contained functional FGF8 and WNT1 proteins that could induce MHB-related genes in differentiating ESCs. The method for generating functional IsO-like cells described in this study could be used to study human central nervous system development and congenital malformations of the midbrain and hindbrain.
引用
收藏
页码:110 / 118
页数:9
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