Modeling psychiatric disorders: from genomic findings to cellular phenotypes

被引:57
|
作者
Falk, A. [1 ]
Heine, V. M. [2 ,3 ]
Harwood, A. J. [4 ,5 ]
Sullivan, P. F. [6 ,7 ,8 ]
Peitz, M. [9 ,10 ]
Bruestle, O. [9 ,10 ]
Shen, S. [11 ]
Sun, Y-M [12 ]
Glover, J. C. [13 ,14 ]
Posthuma, D. [3 ,15 ]
Djurovic, S. [16 ,17 ]
机构
[1] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
[2] Vrije Univ Amsterdam, Med Ctr Amsterdam, Dept Pediat Child Neurol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Neurogen & Cognit Res, Dept Complex Trait Genet, Amsterdam, Netherlands
[4] Cardiff Univ, Neurosci & Mental Hlth Res Inst, Cardiff, S Glam, Wales
[5] Cardiff Univ, Sch Biosci, Cardiff, S Glam, Wales
[6] Univ N Carolina, Dept Genet, Chapel Hill, NC USA
[7] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[8] Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA
[9] Univ Bonn, LIFE & BRAIN Ctr, Inst Reconstruct Neurobiol, Bonn, Germany
[10] German Ctr Neurodegenerat Dis DZNE, Bonn, Germany
[11] NUI Galway, Regenerat Med Inst, Sch Med, Galway, Ireland
[12] Masaryk Univ, Dept Biol, Fac Med, Brno, Czech Republic
[13] Univ Oslo, Dept Mol Med, Oslo, Norway
[14] Oslo Univ Hosp, Norwegian Ctr Stem Cell Res, Oslo, Norway
[15] Vrije Univ, Med Ctr, Dept Clin Genet, Neurosci Campus Amsterdam, Amsterdam, Netherlands
[16] Univ Bergen, Oslo Univ Hosp, Dept Med Genet, Kirkeveien 166,POB 4956 Nydalen, N-0424 Oslo, Norway
[17] Univ Bergen, Dept Clin Sci, KG Jebsen Ctr Psychosis Res, NORMENT, Bergen, Norway
基金
瑞典研究理事会; 英国惠康基金;
关键词
PLURIPOTENT STEM-CELLS; FIBRILLARY ACIDIC PROTEIN; IPSC-DERIVED NEURONS; DE-NOVO MUTATIONS; GENE-EXPRESSION; CORTICAL DEVELOPMENT; NEURAL DEVELOPMENT; BIPOLAR DISORDER; DOWN-REGULATION; SOMATIC-CELLS;
D O I
10.1038/mp.2016.89
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
Major programs in psychiatric genetics have identified 4150 risk loci for psychiatric disorders. These loci converge on a small number of functional pathways, which span conventional diagnostic criteria, suggesting a partly common biology underlying schizophrenia, autism and other psychiatric disorders. Nevertheless, the cellular phenotypes that capture the fundamental features of psychiatric disorders have not yet been determined. Recent advances in genetics and stem cell biology offer new prospects for cell-based modeling of psychiatric disorders. The advent of cell reprogramming and induced pluripotent stem cells (iPSC) provides an opportunity to translate genetic findings into patient-specific in vitro models. iPSC technology is less than a decade old but holds great promise for bridging the gaps between patients, genetics and biology. Despite many obvious advantages, iPSC studies still present multiple challenges. In this expert review, we critically review the challenges for modeling of psychiatric disorders, potential solutions and how iPSC technology can be used to develop an analytical framework for the evaluation and therapeutic manipulation of fundamental disease processes.
引用
收藏
页码:1167 / 1179
页数:13
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