Mouse embryonic stem cells can differentiate via multiple paths to the same state

被引:51
作者
Briggs, James Alexander [1 ]
Li, Victor C. [1 ]
Lee, Seungkyu [2 ,3 ]
Woolf, Clifford J. [2 ,3 ]
Klein, Allon [1 ]
Krischner, Marc W. [1 ]
机构
[1] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Neurobiol, Boston, MA USA
[3] Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA USA
来源
ELIFE | 2017年 / 6卷
基金
美国国家卫生研究院;
关键词
DIRECT CONVERSION; HUMAN FIBROBLASTS; EXPRESSION; FATE; DYNAMICS; NEURONS;
D O I
10.7554/eLife.26945
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In embryonic development, cells differentiate through stereotypical sequences of intermediate states to generate particular mature fates. By contrast, driving differentiation by ectopically expressing terminal transcription factors (direct programming) can generate similar fates by alternative routes. How differentiation in direct programming relates to embryonic differentiation is unclear. We applied single-cell RNA sequencing to compare two motor neuron differentiation protocols: a standard protocol approximating the embryonic lineage, and a direct programming method. Both initially undergo similar early neural commitment. Later, the direct programming path diverges into a novel transitional state rather than following the expected embryonic spinal intermediates. The novel state in direct programming has specific and uncharacteristic gene expression. It forms a loop in gene expression space that converges separately onto the same final motor neuron state as the standard path. Despite their different developmental histories, motor neurons from both protocols structurally, functionally, and transcriptionally resemble motor neurons isolated from embryos.
引用
收藏
页数:23
相关论文
共 33 条
[1]   Single-Cell Trajectory Detection Uncovers Progression and Regulatory Coordination in Human B Cell Development [J].
Bendall, Sean C. ;
Davis, Kara L. ;
Amir, El-ad David ;
Tadmor, Michelle D. ;
Simonds, Erin F. ;
Chen, Tiffany J. ;
Shenfeld, Daniel K. ;
Nolan, Garry P. ;
Pe'er, Dana .
CELL, 2014, 157 (03) :714-725
[2]   Transcriptome-wide noise controls lineage choice in mammalian progenitor cells [J].
Chang, Hannah H. ;
Hemberg, Martin ;
Barahona, Mauricio ;
Ingber, Donald E. ;
Huang, Sui .
NATURE, 2008, 453 (7194) :544-U10
[3]   Turning straw into gold: directing cell fate for regenerative medicine [J].
Cohen, Dena E. ;
Melton, Douglas .
NATURE REVIEWS GENETICS, 2011, 12 (04) :243-252
[4]   How to make spinal motor neurons [J].
Davis-Dusenbery, Brandi N. ;
Williams, Luis A. ;
Klim, Joseph R. ;
Eggan, Kevin .
DEVELOPMENT, 2014, 141 (03) :491-501
[5]   Cell fates as high-dimensional attractor states of a complex gene regulatory network [J].
Huang, S ;
Eichler, G ;
Bar-Yam, Y ;
Ingber, DE .
PHYSICAL REVIEW LETTERS, 2005, 94 (12)
[6]   Bifurcation dynamics in lineage-commitment in bipotent progenitor cells [J].
Huang, Sui ;
Guo, Yan-Ping ;
May, Gillian ;
Enver, Tariq .
DEVELOPMENTAL BIOLOGY, 2007, 305 (02) :695-713
[7]   Direct Reprogramming of Fibroblasts into Functional Cardiomyocytes by Defined Factors [J].
Ieda, Masaki ;
Fu, Ji-Dong ;
Delgado-Olguin, Paul ;
Vedantham, Vasanth ;
Hayashi, Yohei ;
Bruneau, Benoit G. ;
Srivastava, Deepak .
CELL, 2010, 142 (03) :375-386
[8]   Neuronal specification in the spinal cord: Inductive signals and transcriptional codes [J].
Jessell, TM .
NATURE REVIEWS GENETICS, 2000, 1 (01) :20-29
[9]   Droplet Barcoding for Single-Cell Transcriptomics Applied to Embryonic Stem Cells [J].
Klein, Allon M. ;
Mazutis, Linas ;
Akartuna, Ilke ;
Tallapragada, Naren ;
Veres, Adrian ;
Li, Victor ;
Peshkin, Leonid ;
Weitz, David A. ;
Kirschner, Marc W. .
CELL, 2015, 161 (05) :1187-1201
[10]   Lineage Tracing [J].
Kretzschmar, Kai ;
Watt, Fiona M. .
CELL, 2012, 148 (1-2) :33-45