Constructing and Deconstructing Stem Cell Models of Neurological Disease

被引:123
作者
Han, Steve S. W. [1 ,2 ,3 ]
Williams, Luis A. [1 ,2 ]
Eggan, Kevin C. [1 ,2 ]
机构
[1] Harvard Univ, Howard Hughes Med Inst, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[3] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
关键词
SPINAL MUSCULAR-ATROPHY; VALPROIC ACID INCREASES; ZINC-FINGER NUCLEASES; FRAGILE-X-SYNDROME; DIRECTED DIFFERENTIATION; MOTOR-NEURONS; RETT-SYNDROME; HIGHLY EFFICIENT; HUMAN ESCS; GENETIC-MODIFICATION;
D O I
10.1016/j.neuron.2011.05.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Among the disciplines of medicine, the study of neurological disorders is particularly challenging. The fundamental inaccessibility of the human neural types affected by disease prevents their isolation for in vitro studies of degenerative mechanisms or for drug screening efforts. However, the ability to reprogram readily accessible tissue from patients into pluripotent stem (iPS) cells may now provide a general solution to this shortage of human neurons. Gradually improving methods for directing the differentiation of patient-specific stem cells has enabled the production of several neural cell types affected by disease. Furthermore, initial studies with stem cell lines derived from individuals with pediatric, monogenic disorders have validated the stem cell approach to disease modeling, allowing relevant neural phenotypes to be observed and studied. Whether iPS cell-derived neurons will always faithfully recapitulate the same degenerative processes observed in patients and serve as platforms for drug discovery relevant to common late-onset diseases remains to be determined.
引用
收藏
页码:626 / 644
页数:19
相关论文
共 168 条
[1]   MeCP2: structure and function [J].
Adkins, Nicholas L. ;
Georgel, Philippe T. .
BIOCHEMISTRY AND CELL BIOLOGY, 2011, 89 (01) :1-11
[2]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[3]   Neuropathology of Rett syndrome [J].
Armstrong, DD .
JOURNAL OF CHILD NEUROLOGY, 2005, 20 (09) :747-753
[4]   Familial dysautonomia [J].
Axelrod, FB .
MUSCLE & NERVE, 2004, 29 (03) :352-363
[5]   Adaptation to culture of human embryonic stem cells and oncogenesis in vivo [J].
Baker, Duncan E. C. ;
Harrison, Neil J. ;
Maltby, Edna ;
Smith, Kath ;
Moore, Harry D. ;
Shaw, Pamela J. ;
Heath, Paul R. ;
Holden, Hazel ;
Andrews, Peter W. .
NATURE BIOTECHNOLOGY, 2007, 25 (02) :207-215
[6]   Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology [J].
Ballas, Nurit ;
Lioy, Daniel T. ;
Grunseich, Christopher ;
Mandel, Gail .
NATURE NEUROSCIENCE, 2009, 12 (03) :311-317
[7]   Lentiviral vectors harboring a dual-gene system allow high and homogeneous transgene expression in selected polyclonal human embryonic stem cells [J].
Ben-Dor, Israel ;
Itsykson, Pavel ;
Goldenberg, Daniel ;
Galun, Eithan ;
Reubinoff, Benjamin E. .
MOLECULAR THERAPY, 2006, 14 (02) :255-267
[8]   Transplantation of human embryonic stem cell-derived neural progenitors improves behavioral deficit in Parkinsonian rats [J].
Ben-Hur, T ;
Idelson, M ;
Khaner, H ;
Pera, M ;
Reinhartz, E ;
Itzik, A ;
Reubinoff, BE .
STEM CELLS, 2004, 22 (07) :1246-1255
[9]   The Controlled Generation of Functional Basal Forebrain Cholinergic Neurons from Human Embryonic Stem Cells [J].
Bissonnette, Christopher J. ;
Lyass, Ljuba ;
Bhattacharyya, Bula J. ;
Belmadani, Abdelhak ;
Miller, Richard J. ;
Kessler, John A. .
STEM CELLS, 2011, 29 (05) :802-811
[10]   Reference Maps of Human ES and iPS Cell Variation Enable High-Throughput Characterization of Pluripotent Cell Lines [J].
Bock, Christoph ;
Kiskinis, Evangelos ;
Verstappen, Griet ;
Gu, Hongcang ;
Boulting, Gabriella ;
Smith, Zachary D. ;
Ziller, Michael ;
Croft, Gist F. ;
Amoroso, Mackenzie W. ;
Oakley, Derek H. ;
Gnirke, Andreas ;
Eggan, Kevin ;
Meissner, Alexander .
CELL, 2011, 144 (03) :439-452