Induced Neuronal Reprogramming

被引:29
作者
Ang, Cheen Euong [1 ,2 ,3 ]
Wernig, Marius [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Bioengn, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
epigenetic reprogramming; neuronal reprogramming; cell fate; pluripotency; NEURAL STEM-CELLS; DIRECT LINEAGE CONVERSION; ADULT HUMAN FIBROBLASTS; DOPAMINERGIC-NEURONS; MOUSE FIBROBLASTS; DEFINED FACTORS; IN-VIVO; FUNCTIONAL-NEURONS; GLIAL-CELLS; OXYGEN-TENSION;
D O I
10.1002/cne.23620
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cellular differentiation processes during normal embryonic development are guided by extracellular soluble factors such as morphogen gradients and cell contact signals, eventually resulting in induction of specific combinations of lineage-determining transcription factors. The young field of epigenetic reprogramming takes advantage of this knowledge and uses cell fate determination factors to convert one lineage into another such as the conversion of fibroblasts into pluripotent stem cells or neurons. These induced cell fate conversions open up new avenues for studying disease processes, generating cell material for therapeutic intervention such as drug screening and potentially also for cell-based therapies. However, there are still limitations that have to be overcome to fulfill these promises, centering on reprogramming efficiencies, cell identity, and maturation. In this review, we discuss the discovery of induced neuronal reprogramming, ways to improve the conversion process, and finally how to define properly the identity of those converted neuronal cells. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:2877 / 2886
页数:10
相关论文
共 67 条
[1]   Nonviral Direct Conversion of Primary Mouse Embryonic Fibroblasts to Neuronal Cells [J].
Adler, Andrew F. ;
Grigsby, Christopher L. ;
Kulangara, Karina ;
Wang, Hong ;
Yasuda, Ryohei ;
Leong, Kam W. .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2012, 1 :e32
[2]   Direct Reprogramming of Adult Human Fibroblasts to Functional Neurons under Defined Conditions [J].
Ambasudhan, Rajesh ;
Talantova, Maria ;
Coleman, Ronald ;
Yuan, Xu ;
Zhu, Saiyong ;
Lipton, Stuart A. ;
Ding, Sheng .
CELL STEM CELL, 2011, 9 (02) :113-118
[3]   Transcriptional control of midbrain dopaminergic neuron development [J].
Ang, Siew-Lan .
DEVELOPMENT, 2006, 133 (18) :3499-3506
[4]   Functional properties of neurons derived from in vitro reprogrammed postnatal astroglia [J].
Berninger, Benedikt ;
Costa, Marcos R. ;
Koch, Ursula ;
Schroeder, Timm ;
Sutor, Bernd ;
Grothe, Benedikt ;
Goetz, Magdalena .
JOURNAL OF NEUROSCIENCE, 2007, 27 (32) :8654-8664
[5]   Dopamine neuron systems in the brain:: an update [J].
Bjorklund, Anders ;
Dunnett, Stephen B. .
TRENDS IN NEUROSCIENCES, 2007, 30 (05) :194-202
[6]   Neuronal Network Formation from Reprogrammed Early Postnatal Rat Cortical Glial Cells [J].
Blum, Robert ;
Heinrich, Christophe ;
Sanchez, Rodrigo ;
Lepier, Alexandra ;
Gundelfinger, Eckart D. ;
Berninger, Benedikt ;
Goetz, Magdalena .
CEREBRAL CORTEX, 2011, 21 (02) :413-424
[7]   Expression pattern of the transcription factor Olig2 in response to brain injuries:: Implications for neuronal repair [J].
Buffo, A ;
Vosko, MR ;
Ertürk, D ;
Hamann, GF ;
Jucker, M ;
Rowitch, D ;
Götz, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (50) :18183-18188
[8]   Direct generation of functional dopaminergic neurons from mouse and human fibroblasts [J].
Caiazzo, Massimiliano ;
Dell'Anno, Maria Teresa ;
Dvoretskova, Elena ;
Lazarevic, Dejan ;
Taverna, Stefano ;
Leo, Damiana ;
Sotnikova, Tatyana D. ;
Menegon, Andrea ;
Roncaglia, Paola ;
Colciago, Giorgia ;
Russo, Giovanni ;
Carninci, Piero ;
Pezzoli, Gianni ;
Gainetdinov, Raul R. ;
Gustincich, Stefano ;
Dityatev, Alexander ;
Broccoli, Vania .
NATURE, 2011, 476 (7359) :224-U151
[9]  
Chanda S, 2014, STEM CELL R IN PRESS
[10]   Neurons generated by direct conversion of fibroblasts reproduce synaptic phenotype caused by autism-associated neuroligin-3 mutation [J].
Chanda, Soham ;
Marro, Samuele ;
Wernig, Marius ;
Suedhof, Thomas C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (41) :16622-16627