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
相关论文
共 30 条
  • [1] A developmental and genetic classification for midbrain-hindbrain malformations
    Barkovich, A. James
    Millen, Kathleen J.
    Dobyns, William B.
    [J]. BRAIN, 2009, 132 : 3199 - 3230
  • [2] Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences
    Basson, M. Albert
    Wingate, Richard J.
    [J]. FRONTIERS IN NEUROANATOMY, 2013, 7
  • [3] Benjamini Y, 2001, ANN STAT, V29, P1165
  • [4] Genetic control of midbrain dopaminergic neuron development
    Blaess, Sandra
    Ang, Siew-Lan
    [J]. WILEY INTERDISCIPLINARY REVIEWS-DEVELOPMENTAL BIOLOGY, 2015, 4 (02) : 113 - 134
  • [5] The caudal limit of Otx2 expression positions the isthmic organizer
    Broccoli, V
    Boncinelli, E
    Wurst, W
    [J]. NATURE, 1999, 401 (6749) : 164 - 168
  • [6] Sustained interactive Wnt and FGF signaling is required to maintain isthmic identity
    Canning, Claire A.
    Lee, Lily
    Irving, Carol
    Mason, Ivor
    Jones, C. Michael
    [J]. DEVELOPMENTAL BIOLOGY, 2007, 305 (01) : 276 - 286
  • [7] WNTs in the vertebrate nervous system: From patterning to neuronal connectivity
    Ciani, L
    Salinas, PC
    [J]. NATURE REVIEWS NEUROSCIENCE, 2005, 6 (05) : 351 - U17
  • [8] Midbrain development induced by FGF8 in the chick embryo
    Crossley, PH
    Martinez, S
    Martin, GR
    [J]. NATURE, 1996, 380 (6569) : 66 - 68
  • [9] The R-spondin/Lgr5/Rnf43 module: regulator of Wnt signal strength
    de Lau, Wim
    Peng, Weng Chuan
    Gros, Piet
    Clevers, Hans
    [J]. GENES & DEVELOPMENT, 2014, 28 (04) : 305 - 316
  • [10] Irving C, 2000, DEVELOPMENT, V127, P177